gnu: Remove extraneous #:meson build arguments. - guix

diff options

author	Maxim Cournoyer <maxim.cournoyer@gmail.com>	2023-04-08 10:39:49 -0400
committer	Maxim Cournoyer <maxim.cournoyer@gmail.com>	2023-04-09 12:48:29 -0400
commit	46873adc04ccf2c753362ee14c7faa81fed602c4 (patch)
tree	651184fef9b80225495d1d8e8126eea7084b89d4 /gnu/services/sound.scm
parent	03580b5f1d997df066a5119cf0a242f827354ba8 (diff)
download	guix-46873adc04ccf2c753362ee14c7faa81fed602c4.tar.gz guix-46873adc04ccf2c753362ee14c7faa81fed602c4.zip

gnu: Remove extraneous #:meson build arguments.

* gnu/packages/build-tools.scm (meson-python) [propagated-inputs]: Replace meson-0.63 with meson. * gnu/packages/freedesktop.scm (appstream) [arguments]: Remove #:meson argument. * gnu/packages/gnome.scm (raider): Likewise. (komikku): Likewise. * gnu/packages/syndication.scm (syndication-domination): Likewise. * gnu/packages/virtualization.scm (qemu): Likewise. * gnu/packages/xdisorg.scm (tofi): Likewise.

Diffstat (limited to 'gnu/services/sound.scm')

0 files changed, 0 insertions, 0 deletions

#:use-module (gnu packages gawk) #:use-module (gnu packages gcc) #:use-module (gnu packages gd) #:use-module (gnu packages golang) #:use-module (gnu packages golang-build) #:use-module (gnu packages golang-check) #:use-module (gnu packages golang-compression) #:use-module (gnu packages golang-xyz) #:use-module (gnu packages glib) #:use-module (gnu packages graph) #:use-module (gnu packages graphics) #:use-module (gnu packages graphviz) #:use-module (gnu packages groff) #:use-module (gnu packages gtk) #:use-module (gnu packages guile) #:use-module (gnu packages guile-xyz) #:use-module (gnu packages haskell-check) #:use-module (gnu packages haskell-web) #:use-module (gnu packages haskell-xyz) #:use-module (gnu packages image) #:use-module (gnu packages image-processing) #:use-module (gnu packages imagemagick) #:use-module (gnu packages java) #:use-module (gnu packages java-compression) #:use-module (gnu packages java-xml) #:use-module (gnu packages jemalloc) #:use-module (gnu packages jupyter) #:use-module (gnu packages libffi) #:use-module (gnu packages linux) #:use-module (gnu packages llvm) #:use-module (gnu packages logging) #:use-module (gnu packages lsof) #:use-module (gnu packages machine-learning) #:use-module (gnu packages man) #:use-module (gnu packages maths) #:use-module (gnu packages mpi) #:use-module (gnu packages ncurses) #:use-module (gnu packages node) #:use-module (gnu packages ocaml) #:use-module (gnu packages pcre) #:use-module (gnu packages parallel) #:use-module (gnu packages pdf) #:use-module (gnu packages perl) #:use-module (gnu packages perl-check) #:use-module (gnu packages perl-web) #:use-module (gnu packages pkg-config) #:use-module (gnu packages popt) #:use-module (gnu packages protobuf) #:use-module (gnu packages python) #:use-module (gnu packages python-build) #:use-module (gnu packages python-check) #:use-module (gnu packages python-compression) #:use-module (gnu packages python-crypto) #:use-module (gnu packages python-science) #:use-module (gnu packages python-web) #:use-module (gnu packages python-xyz) #:use-module (gnu packages qt) #:use-module (gnu packages rdf) #:use-module (gnu packages readline) #:use-module (gnu packages rpc) #:use-module (gnu packages rsync) #:use-module (gnu packages ruby) #:use-module (gnu packages serialization) #:use-module (gnu packages shells) #:use-module (gnu packages skribilo) #:use-module (gnu packages sphinx) #:use-module (gnu packages sqlite) #:use-module (gnu packages statistics) #:use-module (gnu packages swig) #:use-module (gnu packages tbb) #:use-module (gnu packages tex) #:use-module (gnu packages texinfo) #:use-module (gnu packages textutils) #:use-module (gnu packages time) #:use-module (gnu packages tls) #:use-module (gnu packages uglifyjs) #:use-module (gnu packages video) #:use-module (gnu packages vim) #:use-module (gnu packages web) #:use-module (gnu packages wget) #:use-module (gnu packages xml) #:use-module (gnu packages xorg) #:use-module (guix platform) #:use-module (srfi srfi-1) #:use-module (srfi srfi-26) #:use-module (ice-9 match)) (define-public aragorn (package (name "aragorn") (version "1.2.41") (source (origin (method url-fetch) (uri (string-append "https://www.ansikte.se/ARAGORN/Downloads/" "aragorn" version ".c")) (sha256 (base32 "0jkzx7sqiarydvz3bwaxh790fpvpkfc926dhsza1dbdhq32ir8wj")))) (build-system gnu-build-system) (arguments (list #:tests? #f ; there are no tests #:phases #~(modify-phases %standard-phases (delete 'configure) (replace 'build (lambda _ (invoke "gcc" "-O3" "-ffast-math" "-finline-functions" "-o" "aragorn" #$source))) (replace 'install (lambda* (#:key inputs #:allow-other-keys) (let ((bin (string-append #$output "/bin")) (man (string-append #$output "/share/man/man1"))) (install-file "aragorn" bin) (mkdir-p man) (copy-file (assoc-ref inputs "aragorn.1") (string-append man "/aragorn.1")))))))) (native-inputs `(("aragorn.1" ,(origin (method url-fetch) (uri "https://www.ansikte.se/ARAGORN/Downloads/aragorn.1") (sha256 (base32 "0bn9lapa6f0cl07dbn2fjrapirv9d4bk7w248w39fhb4vbczcc3f")))))) (home-page "https://www.ansikte.se/ARAGORN/") (synopsis "Detect tRNA, mtRNA and tmRNA genes in nucleotide sequences") (description "Aragorn identifies transfer RNA, mitochondrial RNA and transfer-messenger RNA from nucleotide sequences, based on homology to known tRNA consensus sequences and RNA structure. It also outputs the secondary structure of the predicted RNA.") (license license:gpl3+))) (define-public bamtools (package (name "bamtools") (version "2.5.2") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/pezmaster31/bamtools") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "14lw571vbks138i0lj66qjdbk8iwa817x2zbpzij61vv1gdgfbn5")))) (build-system cmake-build-system) (arguments (list #:configure-flags '(list "-DBUILD_SHARED_LIBS=ON"))) (inputs (list jsoncpp zlib)) (native-inputs (list pkg-config)) (home-page "https://github.com/pezmaster31/bamtools") (synopsis "C++ API and command-line toolkit for working with BAM data") (description "BamTools provides both a C++ API and a command-line toolkit for handling BAM files.") (license license:expat))) (define-public bamutils (package (name "bamutils") (version "1.0.15") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/statgen/bamUtil") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "1pxydf9qsr8667jh525bc2wiqn9nwk8rkg05kbyfmjs8d261fl9y")))) (build-system gnu-build-system) (arguments (list #:tests? #f ;fails to link debug libraries #:test-target "test" #:make-flags #~(list (string-append "INSTALLDIR=" #$output "/bin")) #:phases #~(modify-phases %standard-phases (replace 'configure (lambda* (#:key inputs #:allow-other-keys) (substitute* "src/Makefile" (("^DATE=.*") "DATE=\"1970-01-01\"\n")) (copy-recursively (assoc-ref inputs "libstatgen") "../libStatGen")))))) (inputs (list zlib)) (native-inputs `(("libstatgen" ,(origin (method git-fetch) (uri (git-reference (url "https://github.com/statgen/libStatGen/") (commit (string-append "v" version)))) (file-name (git-file-name "libstatgen" version)) (sha256 (base32 "0spvbpvnpxrgj8kajpkhf1mv7kdyvj723y9zh13jykvnjh8a15j3")))))) (home-page "https://genome.sph.umich.edu/wiki/BamUtil") (synopsis "Programs for working on SAM/BAM files") (description "This package provides several programs that perform operations on SAM/BAM files. All of these programs are built into a single executable called @code{bam}.") (license license:gpl3+))) (define-public bcftools (package (name "bcftools") (version "1.14") (source (origin (method url-fetch) (uri (string-append "https://github.com/samtools/bcftools/" "releases/download/" version "/bcftools-" version ".tar.bz2")) (sha256 (base32 "1jqrma16fx8kpvb3c0462dg0asvmiv5yi8myqmc5ddgwi6p8ivxp")) (modules '((guix build utils))) (snippet '(begin ;; Delete bundled htslib. (delete-file-recursively "htslib-1.14"))))) (build-system gnu-build-system) (arguments `(#:configure-flags (list "--enable-libgsl") #:test-target "test" #:phases (modify-phases %standard-phases (add-before 'check 'patch-tests (lambda _ (substitute* "test/test.pl" (("/bin/bash") (which "bash")))))))) (native-inputs (list htslib perl)) (inputs (list gsl zlib)) (home-page "https://samtools.github.io/bcftools/") (synopsis "Utilities for variant calling and manipulating VCFs and BCFs") (description "BCFtools is a set of utilities that manipulate variant calls in the Variant Call Format (VCF) and its binary counterpart BCF. All commands work transparently with both VCFs and BCFs, both uncompressed and BGZF-compressed.") ;; The sources are dual MIT/GPL, but becomes GPL-only when USE_GPL=1. (license (list license:gpl3+ license:expat)))) (define-public bcftools-1.12 (package/inherit bcftools (version "1.12") (source (origin (method url-fetch) (uri (string-append "https://github.com/samtools/bcftools/" "releases/download/" version "/bcftools-" version ".tar.bz2")) (sha256 (base32 "1x94l1hy2pi3lbz0sxlbw0g6q5z5apcrhrlcwda94ns9n4r6a3ks")) (modules '((guix build utils))) (snippet '(begin ;; Delete bundled htslib. (delete-file-recursively "htslib-1.12"))))) (native-inputs (list htslib-1.12 perl)))) (define-public bcftools-1.10 (package/inherit bcftools (version "1.10") (source (origin (method url-fetch) (uri (string-append "https://github.com/samtools/bcftools/" "releases/download/" version "/bcftools-" version ".tar.bz2")) (sha256 (base32 "10xgwfdgqb6dsmr3ndnpb77mc3a38dy8kh2c6czn6wj7jhdp4dra")) (modules '((guix build utils))) (snippet '(begin ;; Delete bundled htslib. (delete-file-recursively "htslib-1.10"))))) (native-inputs (list htslib-1.10 perl)))) (define-public bedops (package (name "bedops") (version "2.4.41") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/bedops/bedops") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "046037qdxsn01ln28rbrwnc7wq4a3xahmb2k74l0w75dby5ni42l")))) (build-system gnu-build-system) (arguments (list ;; We cannot run the tests because the build system makes strange ;; assumptions about where executables are located. #:tests? #false #:test-target "tests" #:make-flags #~(list (string-append "CC=" #$(cc-for-target))) #:phases #~(modify-phases %standard-phases (add-after 'unpack 'unpack-tarballs (lambda _ ;; FIXME: Bedops includes tarballs of minimally patched upstream ;; libraries jansson, zlib, and bzip2. We cannot just use stock ;; libraries because at least one of the libraries (zlib) is ;; patched to add a C++ function definition (deflateInit2cpp). ;; Until the Bedops developers offer a way to link against system ;; libraries we have to build the in-tree copies of these three ;; libraries. ;; See upstream discussion: ;; https://github.com/bedops/bedops/issues/124 ;; Unpack the tarballs to benefit from shebang patching. (with-directory-excursion "third-party" (invoke "tar" "xvf" "jansson-2.6.tar.bz2") (invoke "tar" "xvf" "zlib-1.2.7.tar.bz2") (invoke "tar" "xvf" "bzip2-1.0.6.tar.bz2")) ;; Disable unpacking of tarballs in Makefile. (substitute* "system.mk/Makefile.linux" (("^\tbzcat .*") "\t@echo \"not unpacking\"\n") (("\\./configure") "CONFIG_SHELL=bash ./configure")) (substitute* "third-party/zlib-1.2.7/Makefile.in" (("^SHELL=.*$") "SHELL=bash\n")))) (delete 'configure) (replace 'install (lambda _ (invoke "make" "install" (string-append "BINDIR=" #$output "/bin"))))))) (native-inputs (list diffutils perl which)) (home-page "https://github.com/bedops/bedops") (synopsis "Tools for high-performance genomic feature operations") (description "BEDOPS is a suite of tools to address common questions raised in genomic studies---mostly with regard to overlap and proximity relationships between data sets. It aims to be scalable and flexible, facilitating the efficient and accurate analysis and management of large-scale genomic data. BEDOPS provides tools that perform highly efficient and scalable Boolean and other set operations, statistical calculations, archiving, conversion and other management of genomic data of arbitrary scale. Tasks can be easily split by chromosome for distributing whole-genome analyses across a computational cluster.") (license license:gpl2+))) (define-public bedtools (package (name "bedtools") (version "2.30.0") (source (origin (method url-fetch) (uri (string-append "https://github.com/arq5x/bedtools2/releases/" "download/v" version "/" "bedtools-" version ".tar.gz")) (sha256 (base32 "1f2hh79l7dn147c2xyfgf5wfjvlqfw32kjfnnh2n1qy6rpzx2fik")))) (build-system gnu-build-system) (arguments (list #:test-target "test" #:make-flags #~(list (string-append "prefix=" #$output)) #:phases '(modify-phases %standard-phases (delete 'configure)))) (native-inputs (list python-wrapper)) (inputs (list samtools zlib)) (home-page "https://github.com/arq5x/bedtools2") (synopsis "Tools for genome analysis and arithmetic") (description "Collectively, the bedtools utilities are a swiss-army knife of tools for a wide-range of genomics analysis tasks. The most widely-used tools enable genome arithmetic: that is, set theory on the genome. For example, bedtools allows one to intersect, merge, count, complement, and shuffle genomic intervals from multiple files in widely-used genomic file formats such as BAM, BED, GFF/GTF, VCF.") (license license:expat))) ;; Later releases of bedtools produce files with more columns than ;; what Ribotaper expects. (define-public bedtools-2.18 (package (inherit bedtools) (name "bedtools") (version "2.18.0") (source (origin (method url-fetch) (uri (string-append "https://github.com/arq5x/bedtools2/" "releases/download/v" version "/bedtools-" version ".tar.gz")) (sha256 (base32 "11rvca19ncg03kxd0wzlfx5ws7r3nisd0z8s9j9n182d8ksp2pxz")))) (arguments (list #:test-target "test" #:phases #~(modify-phases %standard-phases (add-after 'unpack 'compatibility (lambda _ (substitute* "src/utils/fileType/FileRecordTypeChecker.h" (("static const float PERCENTAGE") "static constexpr float PERCENTAGE")) (substitute* "src/utils/general/DualQueue.h" (("template <class T, template<class T> class CompareFunc>") "template <class T, template<class U> class CompareFunc>")) (substitute* '("src/utils/BamTools/src/api/algorithms/Sort.h" "src/utils/BamTools/src/api/internal/bam/BamMultiMerger_p.h") (("(bool operator\$\$.*) \\{" m pre) (string-append pre " const {"))))) (delete 'configure) (replace 'install (lambda _ (let ((bin (string-append #$output "/bin/"))) (for-each (lambda (file) (install-file file bin)) (find-files "bin" ".*")))))))) (native-inputs (list python-wrapper)) (inputs (list samtools zlib)))) (define-public bitmapperbs (package (name "bitmapperbs") (version "1.0.2.3") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/chhylp123/BitMapperBS/") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "02ksssfnvmpskld0a2016smfz5nrzm3d90v8974f3cpzywckvp8v")) (modules '((guix build utils))) ;; This package bundles a modified copy of htslib, so we cannot ;; unbundle it. (snippet '(begin (delete-file-recursively "libdivsufsort-2.0.1") (delete-file-recursively "pSAscan-0.1.0"))))) (build-system gnu-build-system) (arguments (list #:tests? #false #:make-flags '(list "bitmapperBS") ;; The build system checks for CPU features. For this reason, we want ;; users to build it locally instead of using substitutes. #:substitutable? #false #:phases #~(modify-phases %standard-phases (add-after 'unpack 'fix-build-system (lambda _ (substitute* "Makefile" (("make prefix=../htslib_aim install") (string-append "make prefix=" #$output " install-so")) (("htslib_aim/include") "htslib") (("htslib_aim/lib") (string-append #$output "/lib"))))) (add-after 'unpack 'patch-references-to-psascan (lambda* (#:key inputs #:allow-other-keys) (substitute* "Makefile" (("\"(./)?psascan" pre all) (string-append "\"" pre (search-input-file inputs "/bin/psascan")))))) (delete 'configure) (replace 'install (lambda _ (install-file "bitmapperBS" (string-append #$output "/bin/"))))))) (inputs (list libdivsufsort psascan zlib)) (home-page "https://github.com/chhylp123/BitMapperBS/") (synopsis "Read aligner for whole-genome bisulfite sequencing") (description "BitMapperBS is memory-efficient aligner that is designed for whole-genome bisulfite sequencing (WGBS) reads from directional protocol.") (supported-systems '("x86_64-linux")) (license license:asl2.0))) (define-public bustools (package (name "bustools") (version "0.43.2") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/BUStools/bustools") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "068kjlc4d528269nl5mc3j8h2c95r1v545d3fi1iw1ckg8rba0hg")))) (build-system cmake-build-system) (arguments (list #:tests? #f)) ;no test target (inputs (list zlib)) (home-page "https://bustools.github.io") (synopsis "Tools for working with BUS files") (description "bustools is a program for manipulating BUS files for single cell RNA-Seq datasets. It can be used to error correct barcodes, collapse UMIs, produce gene count or transcript compatibility count matrices, and is useful for many other tasks.") (license license:bsd-2))) (define-public cellsnp-lite ;; Last release is from November 2021 and does not contain fixes. (let ((commit "0885d746b0b1ea65c8ef92f8943ca7669ca9734a") (revision "0")) (package (name "cellsnp-lite") (version (git-version "1.2.2" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/single-cell-genetics/cellsnp-lite") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "1qrvqgbvw6mbhpyqvqbmvv8dmyc67bsk1041cn7ib6zmd47qm444")))) (build-system gnu-build-system) (arguments (list #:configure-flags #~(list (string-append "--with-htslib=" #$(this-package-input "htslib"))))) (inputs (list curl htslib openssl zlib)) (native-inputs (list autoconf)) (home-page "https://cellsnp-lite.readthedocs.io") (synopsis "Pileup expresses alleles in single-cell or bulk RNA-seq data") (description "This package is designed to pileup the expressed alleles in single-cell or bulk RNA-seq data, which can be directly used for donor deconvolution in multiplexed single-cell RNA-seq data, particularly with other packages, which assigns cells to donors and detects doublets as vireo, even without genotyping reference. This package is the C version of the deprecated cellSNP implemented in Python. Compared to cellSNP, this package is more efficient with higher speed and less memory usage.") (license license:asl2.0)))) (define-public cpat (package (name "cpat") (version "3.0.4") (source (origin (method url-fetch) (uri (pypi-uri "CPAT" version)) (sha256 (base32 "0dfrwwbhv1n4nh2a903d1qfb30fgxgya89sa70aci3wzf8h2z0vd")) (modules '((guix build utils))) (snippet '(for-each delete-file-recursively (list ".eggs" "lib/__pycache__/" "lib/cpmodule/__pycache__/"))))) (build-system pyproject-build-system) (arguments (list #:phases '(modify-phases %standard-phases (replace 'check (lambda* (#:key tests? #:allow-other-keys) (when tests? (with-directory-excursion "test" ;; There is no test4.fa (substitute* "test.sh" ((".*-g test4.fa.*") "")) (invoke "bash" "test.sh")))))))) (propagated-inputs (list python-numpy python-pysam)) (inputs (list r-minimal)) (home-page "https://wlcb.oit.uci.edu/cpat/") (synopsis "Alignment-free distinction between coding and noncoding RNA") (description "CPAT is a method to distinguish coding and noncoding RNA by using a logistic regression model based on four pure sequence-based, linguistic features: ORF size, ORF coverage, Ficket TESTCODE, and Hexamer usage bias. Linguistic features based method does not require other genomes or protein databases to perform alignment and is more robust. Because it is alignment-free, it runs much faster and also easier to use.") (license license:gpl2+))) (define-public pbcopper (package (name "pbcopper") (version "2.0.0") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/PacificBiosciences/pbcopper") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "04mgmla96bsmr9gijbn3ibspry625cv4kqqxv70z4jq4qc407jy3")))) (build-system meson-build-system) (arguments `(#:phases (modify-phases %standard-phases (add-after 'unpack 'patch-meson-files (lambda _ (substitute* "meson.build" (("-msse4.1") ""))))))) (inputs (list boost)) (native-inputs (list googletest pkg-config)) (home-page "https://github.com/PacificBiosciences/pbcopper") (synopsis "Data structures, algorithms, and utilities for PacBio C++ applications") (description "The pbcopper library provides a suite of data structures, algorithms, and utilities for PacBio C++ applications.") (license license:bsd-3))) (define-public r-anndatar (let ((commit "5c3eb7e498d0d9bf1c522ad66f4eb8ad277238b6") (revision "1")) (package (name "r-anndatar") (version (git-version "0.99.0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/scverse/anndataR") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0sx87i8cb4p08ihgpgflxs0fhkr1kw6lxvky4w766rq7wqy41cgk")))) (properties `((upstream-name . "anndataR"))) (build-system r-build-system) (propagated-inputs (list r-matrix r-r6)) (native-inputs (list r-knitr)) (home-page "https://github.com/scverse/anndataR") (synopsis "AnnData interoperability in R") (description "This package aims to bring the power and flexibility of @code{AnnData} to the R ecosystem, allowing you to effortlessly manipulate and analyze your single-cell data. This package lets you work with backed h5ad and zarr files, directly access various slots (e.g. X, obs, var), or convert the data into @code{SingleCellExperiment} and Seurat objects.") (license license:expat)))) (define-public r-anpan (let ((commit "286b88dcf5e9e963a595482139aade154ee1dc86") (revision "1")) (package (name "r-anpan") (version (git-version "0.3.0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/biobakery/anpan") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "10nw5v69gn4pxb4g5gd8nh9r1ywd6yczapl3dpdfms0434wcmkxm")))) (properties `((upstream-name . "anpan"))) (build-system r-build-system) (propagated-inputs (list r-ape r-cmdstanr r-data-table r-dplyr r-fastglm r-furrr r-future r-ggdendro r-ggnewscale r-ggplot2 r-loo r-mass r-patchwork r-phylogram r-posterior r-progressr r-purrr r-r-utils r-stringr r-tibble r-tidyselect)) (native-inputs (list r-knitr)) (home-page "https://github.com/biobakery/anpan") (synopsis "Quantifying microbial strain-host associations") (description "The goal of anpan is to consolidate statistical methods for strain analysis. This includes automated filtering of metagenomic functional profiles, testing genetic elements for association with outcomes, phylogenetic association testing, and pathway-level random effects models.") (license license:expat)))) (define-public r-bedtorch (let ((commit "f5ff4f83b94f59eac660333c64e4b2f296b35cea") (revision "1")) (package (name "r-bedtorch") (version (git-version "0.1.12.12" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/haizi-zh/bedtorch/") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "08l04iqf54b5995gc7rvqqd7w327fwqs7qjyhc9y5cqfj8yv4c48")))) (properties `((upstream-name . "bedtorch"))) (build-system r-build-system) (propagated-inputs (list r-assertthat r-curl r-data-table r-dplyr r-genomeinfodb r-genomicranges r-purrr r-r-utils r-rcpp r-rcurl r-readr r-rhtslib12 r-s4vectors r-stringr r-tidyr)) (home-page "https://github.com/haizi-zh/bedtorch/") (synopsis "R package for fast BED-file manipulation") (description "The goal of bedtorch is to provide a fast BED file manipulation tool suite native in R.") (license license:expat)))) (define-public r-bpcells (let ((commit "32ce67312185d3ed1046b4218dd3aaf1b35dcfda") (revision "1")) (package (name "r-bpcells") (version (git-version "0.1.0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/bnprks/BPCells/") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0im4sqvbii326acmd1hnimyzsllnbvnh9al3dp1nla6isgi7s6cg")))) (properties `((upstream-name . "BPCells"))) (build-system r-build-system) (arguments (list #:phases '(modify-phases %standard-phases (add-after 'unpack 'do-not-tune (lambda _ (substitute* "configure" (("\"-march=native\"") "\"\""))))))) (inputs (list hdf5 zlib)) (propagated-inputs (list r-dplyr r-ggplot2 r-ggrepel r-hexbin r-magrittr r-matrix r-patchwork r-rcolorbrewer r-rcpp r-rcppeigen r-rlang r-scales r-scattermore r-stringr r-tibble r-tidyr r-vctrs)) (native-inputs (list pkg-config)) (home-page "https://github.com/bnprks/BPCells/") (synopsis "Single cell counts matrices to PCA") (description "This is a package providing efficient operations for single cell ATAC-seq fragments and RNA counts matrices. It is interoperable with standard file formats, and introduces efficient bit-packed formats that allow large storage savings and increased read speeds.") (license license:gpl3)))) (define-public r-btools (let ((commit "fa21d4ca01d37ea4d98b45582453f3bf95cbc2b5") (revision "1")) (package (name "r-btools") (version (git-version "0.0.1" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/twbattaglia/btools") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0bca593dnxz6xdywpdi0ipli0paln2b3bfxxj0csnmj55ryrz428")))) (properties `((upstream-name . "btools"))) (build-system r-build-system) (propagated-inputs (list r-biomformat r-coin r-deseq2 r-dplyr r-genefilter r-phyloseq r-picante r-plotly r-reshape2 r-stringr r-vegan)) (home-page "https://github.com/twbattaglia/btools") (synopsis "R functions for microbial diversity analyses") (description "This package provides an assortment of R functions that is suitable for all types of microbial diversity analyses.") (license license:expat)))) (define-public r-codeandroll2 (let ((commit "d58e258851a5c0b430e8620d34dbeefb597c548f") (revision "1")) (package (name "r-codeandroll2") (version (git-version "2.3.6" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/vertesy/CodeAndRoll2") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0sy88mfgw6qqhpnlc5020qzr1jllkcrxfhl2lw42bkl5nb56is71")))) (properties `((upstream-name . "CodeAndRoll2"))) (build-system r-build-system) (propagated-inputs (list r-colorramps r-dplyr r-gplots r-gtools r-plyr r-rcolorbrewer r-sessioninfo r-sm r-stringendo r-stringr)) (home-page "https://github.com/vertesy/CodeAndRoll2") (synopsis "CodeAndRoll2 for vector, matrix and list manipulations") (description "CodeAndRoll2 is a set of more than 130 productivity functions. These functions are used by MarkdownReports, ggExpress, and SeuratUtils.") (license license:gpl3)))) (define-public r-conospanel (let ((commit "39e76b201a783b4e92fd615010a735a61746fbb9") (revision "1")) (package (name "r-conospanel") (version (git-version "1.0.0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/kharchenkolab/conosPanel") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "1zf0aj5d4iaxc3ghvjnaja5qby1avlmljzh94bpyvxbd359z9snn")))) (properties `((upstream-name . "conosPanel"))) (build-system r-build-system) (home-page "https://github.com/kharchenkolab/conosPanel") (synopsis "Data for the conos package") (description "The data within this package is a panel of four samples, each with 3000 cells. There are two samples which are bone marrow (BM), and two samples which are cord blood (CB).") (license license:gpl3)))) (define-public r-conqur (let ((commit "c7a88794efd4ecfe4d96988dceeec3b410222e48") (revision "1")) (package (name "r-conqur") (version (git-version "2.0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/wdl2459/ConQuR") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "19a7p2l67mgjy99i5ksjxlhzaqmrnyi1vzvwnhgnx2jrr6crj7rq")))) (properties `((upstream-name . "ConQuR"))) (build-system r-build-system) (propagated-inputs (list r-ade4 r-ape r-compositions r-cqrreg r-doparallel r-dplyr r-fastdummies r-glmnet r-gplots r-gunifrac r-quantreg r-randomforest r-rocr r-vegan)) (native-inputs (list r-knitr)) (home-page "https://github.com/wdl2459/ConQuR") (synopsis "Batch effects removal for microbiome data") (description "This package conducts batch effects removal from a taxa read count table by a conditional quantile regression method. The distributional attributes of microbiome data - zero-inflation and over-dispersion, are simultaneously considered.") (license license:gpl3)))) (define-public r-ewastools (let ((commit "f7646cacd73266708479b3fea5d625054d179f95") (revision "1")) (package (name "r-ewastools") (version (git-version "1.7.2" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/hhhh5/ewastools/") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0irarlnxfnasa755adxsn67rxsy01zwhjhw18g4cag08cqiyyw41")))) (properties `((upstream-name . "ewastools"))) (build-system r-build-system) (propagated-inputs (list r-data-table r-igraph r-illuminaio r-mblm r-quadprog)) (native-inputs (list r-knitr)) (home-page "https://github.com/hhhh5/ewastools/") (synopsis "Quality control toolset for the Illumina Infinium DNA methylation") (description "This package provides a collection of useful functions for working with DNA methylation micro-array data.") (license license:unlicense)))) (define-public r-numbat (let ((commit "4ab7752e7d267a3f443756675728521a9b0a7295") (revision "1")) (package (name "r-numbat") (version (git-version "1.3.2-1" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/kharchenkolab/numbat") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0wa2cz5iy570r2a57bd74jramxayvfhmxznb0vq4vyk1ia8l5jd1")))) (properties `((upstream-name . "numbat"))) (build-system r-build-system) (propagated-inputs (list r-ape r-catools r-data-table r-dendextend r-dplyr r-genomicranges r-ggplot2 r-ggraph r-ggtree r-glue r-igraph r-iranges r-logger r-magrittr r-matrix r-optparse r-paralleldist r-patchwork r-pryr r-purrr r-r-utils r-rcpp r-rcpparmadillo r-rhpcblasctl r-roptim r-scales r-scistreer r-stringr r-tibble r-tidygraph r-tidyr r-vcfr r-zoo)) (home-page "https://github.com/kharchenkolab/numbat") (synopsis "Haplotype-Aware CNV Analysis from scRNA-Seq") (description "This package provides a computational method that infers copy number variations (CNVs) in cancer scRNA-seq data and reconstructs the tumor phylogeny. numbat integrates signals from gene expression, allelic ratio, and population haplotype structures to accurately infer allele-specific CNVs in single cells and reconstruct their lineage relationship. numbat can be used to: @enumerate @item detect allele-specific copy number variations from single-cells; @item differentiate tumor versus normal cells in the tumor microenvironment; @item infer the clonal architecture and evolutionary history of profiled tumors. @end enumerate numbat does not require tumor/normal-paired DNA or genotype data, but operates solely on the donor scRNA-data data (for example, 10x Cell Ranger output).") (license license:expat)))) (define-public r-p2data (let ((commit "7d4c0e17d7899f9d9b08ab2bf455abe150912f4c") (revision "1")) (package (name "r-p2data") (version (git-version "1.0.0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/kharchenkolab/p2data") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "1hadrldldxvhqs43aqs3c88bqfgql3wcfkbll3jz7fh6z7p3x324")))) (properties `((upstream-name . "p2data"))) (build-system r-build-system) (home-page "https://github.com/kharchenkolab/p2data") (synopsis "Data for pagoda2") (description "This package contains data used by pagoda2. The data within this package are the 3000 bone marrow cells used for vignettes.") (license license:gpl3)))) (define-public r-rhtslib12 (let ((commit "ee186daf04876969c7f31c16a0e0fda8e7c16a30") (revision "1")) (package (name "r-rhtslib12") (version (git-version "1.23.2" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/haizi-zh/Rhtslib12") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0a3kkp0phi2fq6ip8p9vfj3axn7l15f2mb51a6v3ai4nlkhqqawj")))) (properties `((upstream-name . "Rhtslib12"))) (build-system r-build-system) (propagated-inputs (list curl zlib r-zlibbioc)) (native-inputs (list pkg-config r-knitr)) (home-page "https://github.com/haizi-zh/Rhtslib12") (synopsis "HTSlib high-throughput sequencing library as an R package") (description "This package provides version 1.12 of the HTSlib C library for high-throughput sequence analysis. The package is primarily useful to developers of other R packages who wish to make use of HTSlib.") (license license:lgpl2.0+)))) (define-public r-scenic (let ((commit "cedf8490a634da550cea2c831544e5f7f14467d2") (revision "1")) (package (name "r-scenic") (version (git-version "1.3.1" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/aertslab/SCENIC") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "17ai0q260hdqbvm1km1s5dw93pgz4f546ycfii57jyy9m9jka7r0")))) (properties `((upstream-name . "SCENIC"))) (build-system r-build-system) (propagated-inputs (list r-aucell r-data-table r-dynamictreecut r-genie3 r-ggrepel r-mixtools r-nmf r-rcistarget r-rtsne)) (native-inputs (list r-knitr)) (home-page "https://github.com/aertslab/SCENIC") (synopsis "SCENIC (Single Cell rEgulatory Network Inference and Clustering)") (description "SCENIC (Single-cell regulatory network inference and clustering) is an R package to infer Gene Regulatory Networks and cell types from single-cell RNA-seq data.") ;; As of commit cedf8490a634da550cea2c831544e5f7f14467d2 the license is ;; GPLv3. (license license:gpl3)))) (define-public r-scent (let ((commit "f01f18ac30f8a9bcf85b738c6c7815017e2c8ee5") (revision "1")) (package (name "r-scent") (version (git-version "1.0.0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/immunogenomics/SCENT") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "18krksy8ac7yy8hghzaxscj91c61j195yg7j60zswdq97islvfzi")))) (properties `((upstream-name . "SCENT"))) (build-system r-build-system) (inputs (list bedtools)) (propagated-inputs (list r-boot r-data-table r-hmisc r-lme4 r-mass r-matrix r-r-utils r-stringr)) (native-inputs (list r-knitr)) (home-page "https://github.com/immunogenomics/SCENT") (synopsis "Single-Cell enhancer target gene mapping for multimodal single-cell data") (description "This package contains functions for the SCENT algorithm. SCENT uses single-cell multimodal data and links ATAC-seq peaks to their target genes by modeling association between chromatin accessibility and gene expression across individual single cells.") (license license:expat)))) (define-public r-saige (let ((commit "c6717ba9c5a967bcf612e97566d845397b1b7167") (revision "1")) (package (name "r-saige") (version (git-version "1.3.4" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/saigegit/SAIGE") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0c3211whqazycs9ivwdz23imj45j4na2xzcfq5l989ykkgmqnjzs")))) (properties `((upstream-name . "SAIGE"))) (build-system r-build-system) (arguments (list #:phases '(modify-phases %standard-phases (add-after 'unpack 'do-not-download-packages (lambda _ ;; Pretend to be a Conda build to avoid having to install ;; things with pip and cget. (setenv "CONDA_BUILD" "1"))) (add-after 'unpack 'link-with-openblas (lambda* (#:key inputs #:allow-other-keys) (substitute* "src/Makevars" (("-llapack") (search-input-file inputs "/lib/libopenblas.so")))))))) (inputs (list openblas savvy superlu zlib zstd)) (propagated-inputs (list r-bh r-data-table r-dplyr r-matrix r-metaskat r-optparse r-qlcmatrix r-rcpp r-rcpparmadillo r-rcppeigen r-rcppparallel r-rhpcblasctl r-rsqlite r-skat r-spatest)) (home-page "https://github.com/saigegit/SAIGE") (synopsis "Genome-wide association tests in large-scale data sets") (description "SAIGE is a package for efficiently controlling for case-control imbalance and sample relatedness in single-variant assoc tests (SAIGE) and controlling for sample relatedness in region-based assoc tests in large cohorts and biobanks (SAIGE-GENE+).") (license license:gpl2+)))) (define-public r-singlet (let ((commit "765a6c45081807a1522f0e8983e2417822a36f36") (revision "1")) (package (name "r-singlet") (version (git-version "0.99.26" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/zdebruine/singlet") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "040v8wzl9qr8ribr6qss61fz4698d14cqs8nxbc8hqwiqlpy3vs4")))) (properties `((upstream-name . "singlet"))) (build-system r-build-system) (propagated-inputs (list r-dplyr r-fgsea r-ggplot2 r-knitr r-limma r-matrix r-msigdbr r-rcpp r-rcppml/devel r-reshape2 r-scuttle r-seurat)) (native-inputs (list r-knitr)) (home-page "https://github.com/zdebruine/singlet") (synopsis "Non-negative Matrix Factorization for single-cell analysis") (description "This is a package for fast @dfn{Non-negative Matrix Factorization} (NMF) with automatic rank-determination for dimension reduction of single-cell data using Seurat, RcppML nmf, SingleCellExperiments and similar.") (license license:gpl2+)))) (define-public r-stacas (package (name "r-stacas") (version "2.2.0") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/carmonalab/STACAS") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "13i0h5i6vlbrb8ndq9gr81560z9d74b2c7m3rjfzls01irjza9hm")))) (properties `((upstream-name . "STACAS"))) (build-system r-build-system) (propagated-inputs (list r-biocneighbors r-biocparallel r-ggplot2 r-ggridges r-pbapply r-r-utils r-seurat)) (home-page "https://github.com/carmonalab/STACAS") (synopsis "Sub-type anchoring correction for alignment in Seurat") (description "This package implements methods for batch correction and integration of scRNA-seq datasets, based on the Seurat anchor-based integration framework. In particular, STACAS is optimized for the integration of heterogenous datasets with only limited overlap between cell sub-types (e.g. TIL sets of CD8 from tumor with CD8/CD4 T cells from lymphnode), for which the default Seurat alignment methods would tend to over-correct biological differences. The 2.0 version of the package allows the users to incorporate explicit information about cell-types in order to assist the integration process.") (license license:gpl3))) (define-public r-stringendo (let ((commit "15594b1bba11048a812874bafec0eea1dcc8618a") (revision "1")) (package (name "r-stringendo") (version (git-version "0.6.0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/vertesy/Stringendo") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "15ij4zf2j9c8m9n4bqhmxkchjh2bhddwjfxngfpwv7c5wjqyi6ir")))) (properties `((upstream-name . "Stringendo"))) (build-system r-build-system) (propagated-inputs (list r-clipr)) (home-page "https://github.com/vertesy/Stringendo") (synopsis "Stringendo is a string parsing library") (description "This package provides string parsing functionalites for generating plotnames, filenames and paths.") (license license:gpl3)))) (define-public r-readwriter (let ((commit "91373c44641014a1ce8e1c3e928747608aae8f54") (revision "1")) (package (name "r-readwriter") (version (git-version "1.5.3" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/vertesy/ReadWriter") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "156kvmplrip0w1zhs9yl5r0ayjipa0blhy614l65hbsjn1lwbskr")))) (properties `((upstream-name . "ReadWriter"))) (build-system r-build-system) (propagated-inputs (list r-gtools r-openxlsx r-readr r-stringendo)) (home-page "https://github.com/vertesy/ReadWriter") (synopsis "Functions to read and write files conveniently") (description "ReadWriter is a set of R functions to read and write files conveniently.") (license license:gpl3)))) (define-public r-streamgraph (let ((commit "76f7173ec89d456ace5943a512e20b1f6810bbcb") (revision "1")) (package (name "r-streamgraph") (version (git-version "0.9.0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/hrbrmstr/streamgraph") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "010rhnby5a9dg08jvlkr65b3p9iipdxi2f5m1k6j53s80p25yvig")))) (properties `((upstream-name . "streamgraph"))) (build-system r-build-system) (propagated-inputs (list r-dplyr r-htmltools r-htmlwidgets r-magrittr r-tidyr r-xts)) (native-inputs (list r-knitr)) (home-page "https://github.com/hrbrmstr/streamgraph") (synopsis "Htmlwidget for building streamgraph visualizations") (description "A streamgraph is a type of stacked area chart. It represents the evolution of a numeric variable for several groups. Areas are usually displayed around a central axis, and edges are rounded to give a flowing shape. This package provides an @code{htmlwidget} for building streamgraph visualizations.") (license license:expat)))) (define-public r-wasabi (let ((commit "8c33cabde8d18c2657cd6e38e7cb834f87cf9846") (revision "1")) (package (name "r-wasabi") (version (git-version "1.0.1" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/COMBINE-lab/wasabi") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0rpdj6n4cnx8n2zl60dzgl638474sg49dknwi9x3qb4g56dpphfa")))) (properties `((upstream-name . "wasabi"))) (build-system r-build-system) (propagated-inputs (list r-data-table r-rhdf5 r-rjson)) (home-page "https://github.com/COMBINE-lab/wasabi") (synopsis "Use Sailfish and Salmon with Sleuth") (description "This package converts the output of the Sailfish and Salmon RNA-seq quantification tools so that it can be used with the Sleuth differential analysis package.") (license license:bsd-3)))) (define-public pbbam (package (name "pbbam") (version "2.1.0") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/PacificBiosciences/pbbam") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "1iyazi3l7dswpfxh39k5j7ydi0ywja0579xz3r6l9kkwz2n1z6dc")))) (build-system meson-build-system) (arguments `(#:phases (modify-phases %standard-phases (add-after 'unpack 'patch-tests (lambda* (#:key inputs #:allow-other-keys) ;; Disable this test. I tried fixing it by including ;; optional_io.hpp, but there's a type error. (substitute* "tests/src/meson.build" (("'test_ReadGroupInfo.cpp',") "")) #; (substitute* "include/pbbam/ReadGroupInfo.h" (("#include <boost/optional.hpp>" m) (string-append m "\n#include <boost/optional/optional_io.hpp>"))) (substitute* '("tests/scripts/cram/_test.py" "tests/scripts/cram/_main.py") (("'/bin/sh'") (string-append "'" (which "sh") "'")))))))) ;; These libraries are listed as "Required" in the pkg-config file. (propagated-inputs (list htslib-1.14 pbcopper zlib)) (inputs (list boost samtools)) (native-inputs (list googletest pkg-config python-wrapper)) ;for tests (home-page "https://github.com/PacificBiosciences/pbbam") (synopsis "Work with PacBio BAM files") (description "The pbbam software package provides components to create, query, and edit PacBio BAM files and associated indices. These components include a core C++ library, bindings for additional languages, and command-line utilities. This library is not intended to be used as a general-purpose BAM utility - all input and output BAMs must adhere to the PacBio BAM format specification. Non-PacBio BAMs will cause exceptions to be thrown.") (license license:bsd-3))) (define-public pbgzip (let ((commit "2b09f97b5f20b6d83c63a5c6b408d152e3982974")) (package (name "pbgzip") (version (git-version "0.0.0" "0" commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/nh13/pbgzip") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "1mlmq0v96irbz71bgw5zcc43g1x32zwnxx21a5p1f1ch4cikw1yd")))) (build-system gnu-build-system) (native-inputs (list autoconf automake)) (inputs (list zlib)) (home-page "https://github.com/nh13/pbgzip") (synopsis "Parallel Block GZIP") (description "This package implements parallel block gzip. For many formats, in particular genomics data formats, data are compressed in fixed-length blocks such that they can be easily indexed based on a (genomic) coordinate order, since typically each block is sorted according to this order. This allows for each block to be individually compressed (deflated), or more importantly, decompressed (inflated), with the latter enabling random retrieval of data in large files (gigabytes to terabytes). @code{pbgzip} is not limited to any particular format, but certain features are tailored to genomics data formats when enabled. Parallel decompression is somewhat faster, but the true speedup comes during compression.") (license license:expat)))) (define-public blasr-libcpp (package (name "blasr-libcpp") (version "5.3.5") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/PacificBiosciences/blasr_libcpp") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "07cdfnfl29zf2j7fpaaqaxghq3p0wnc109razs0icwm2q6l3gycb")))) (build-system meson-build-system) (arguments `(#:phases (modify-phases %standard-phases (add-after 'unpack 'link-with-hdf5 (lambda* (#:key inputs #:allow-other-keys) (let ((hdf5 (assoc-ref inputs "hdf5"))) (substitute* "meson.build" (("libblasr_deps = \\[" m) (string-append m (format #f "cpp.find_library('hdf5', dirs : '~a'), \ cpp.find_library('hdf5_cpp', dirs : '~a'), " hdf5 hdf5))))))) (add-after 'unpack 'find-googletest (lambda* (#:key inputs #:allow-other-keys) ;; It doesn't find gtest_main because there's no pkg-config file ;; for it. Find it another way. (substitute* "unittest/meson.build" (("libblasr_gtest_dep = dependency\\('gtest_main'.*") (format #f "cpp = meson.get_compiler('cpp') libblasr_gtest_dep = cpp.find_library('gtest_main', dirs : '~a')\n" (assoc-ref inputs "googletest"))))))) ;; TODO: unittest/libblasr_unittest cannot be linked ;; ld: ;; unittest/df08227@@libblasr_unittest@exe/alignment_utils_FileUtils_gtest.cpp.o: ;; undefined reference to symbol ;; '_ZN7testing8internal9DeathTest6CreateEPKcPKNS0_2REES3_iPPS1_' ;; ld: /gnu/store/...-googletest-1.8.0/lib/libgtest.so: ;; error adding symbols: DSO missing from command line #:tests? #f #:configure-flags '("-Dtests=false"))) (inputs (list boost hdf5 htslib pbbam zlib)) (native-inputs (list googletest pkg-config)) (home-page (string-append "https://web.archive.org/web/20201106122415/" "https://github.com/PacificBiosciences/blasr_libcpp")) (synopsis "Library for analyzing PacBio genomic sequences") (description "This package provides three libraries used by applications for analyzing PacBio genomic sequences. This library contains three sub-libraries: pbdata, hdf and alignment.") (license license:bsd-3))) (define-public blasr (package (name "blasr") (version "5.3.5") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/PacificBiosciences/blasr") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "0axyd06gn2xa0p0k76fihsbxpfxvhlb18jn6bf97c0ii58r1wc0k")))) (build-system meson-build-system) (arguments `(#:phases (modify-phases %standard-phases (add-after 'unpack 'link-with-hdf5 (lambda* (#:key inputs #:allow-other-keys) (let ((hdf5 (assoc-ref inputs "hdf5"))) (substitute* "meson.build" (("blasr_deps = \\[" m) (string-append m (format #f "cpp.find_library('hdf5', dirs : '~a'), \ cpp.find_library('hdf5_cpp', dirs : '~a'), " hdf5 hdf5)))))))) ;; Tests require "cram" executable, which is not packaged. #:tests? #f #:configure-flags '("-Dtests=false"))) (inputs (list boost blasr-libcpp hdf5 pbbam zlib)) (native-inputs (list pkg-config)) (home-page (string-append "https://web.archive.org/web/20210813124135/" "https://github.com/PacificBiosciences/blasr")) (synopsis "PacBio long read aligner") (description "Blasr is a genomic sequence aligner for processing PacBio long reads.") (license license:bsd-3))) (define-public randfold (package (name "randfold") (version "2.0.1") (source (origin (method url-fetch) (uri (string-append "http://bioinformatics.psb.ugent.be/" "supplementary_data/erbon/nov2003/downloads/" "randfold-" version ".tar.gz")) (sha256 (base32 "0gqixl4ncaibrxmn25d6lm2hrw4ml2fj13nrc9q1kilsxdfi91mj")))) (build-system gnu-build-system) (arguments (list #:tests? #f ;no tests provided #:phases #~(modify-phases %standard-phases (delete 'configure) (replace 'install (lambda _ (install-file "randfold" (string-append #$output "/bin"))))))) (inputs (list eddylab-squid)) (home-page "http://bioinformatics.psb.ugent.be/supplementary_data/erbon/nov2003/") (synopsis "Minimum free energy of folding randomization test software") (description "randfold computes the probability that, for a given sequence, the @dfn{Minimum Free Energy} (MFE) of the secondary structure is different from MFE computed with random sequences.") (license license:gpl2))) (define-public ribotaper (package (name "ribotaper") (version "1.3.1") (source (origin (method url-fetch) (uri (string-append "https://ohlerlab.mdc-berlin.de/" "files/RiboTaper/RiboTaper_Version_" version ".tar.gz")) (sha256 (base32 "0ykjbps1y3z3085q94npw8i9x5gldc6shy8vlc08v76zljsm07hv")))) (build-system gnu-build-system) (arguments (list #:phases #~(modify-phases %standard-phases (add-after 'install 'wrap-executables (lambda _ (for-each (lambda (script) (wrap-program (string-append #$output "/bin/" script) `("R_LIBS_SITE" ":" = (,(getenv "R_LIBS_SITE"))))) '("create_annotations_files.bash" "create_metaplots.bash" "Ribotaper_ORF_find.sh" "Ribotaper.sh"))))))) (inputs (list bash-minimal bedtools-2.18 samtools-0.1 r-minimal r-foreach r-xnomial r-domc r-multitaper r-seqinr)) (home-page "https://ohlerlab.mdc-berlin.de/software/RiboTaper_126/") (synopsis "Define translated ORFs using ribosome profiling data") (description "Ribotaper is a method for defining translated @dfn{open reading frames} (ORFs) using ribosome profiling (ribo-seq) data. This package provides the Ribotaper pipeline.") (license license:gpl3+))) (define-public bioawk (package (name "bioawk") (version "1.0") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/lh3/bioawk") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "1pxc3zdnirxbf9a0az698hd8xdik7qkhypm7v6hn922x8y9qmspm")))) (build-system gnu-build-system) (inputs (list zlib)) (native-inputs (list bison)) (arguments (list #:tests? #f ; There are no tests to run. ;; Bison must generate files, before other targets can build. #:parallel-build? #f #:phases #~(modify-phases %standard-phases (delete 'configure) ; There is no configure phase. (replace 'install (lambda _ (let ((bin (string-append #$output "/bin")) (man (string-append #$output "/share/man/man1"))) (mkdir-p man) (copy-file "awk.1" (string-append man "/bioawk.1")) (install-file "bioawk" bin))))))) (home-page "https://github.com/lh3/bioawk") (synopsis "AWK with bioinformatics extensions") (description "Bioawk is an extension to Brian Kernighan's awk, adding the support of several common biological data formats, including optionally gzip'ed BED, GFF, SAM, VCF, FASTA/Q and TAB-delimited formats with column names. It also adds a few built-in functions and a command line option to use TAB as the input/output delimiter. When the new functionality is not used, bioawk is intended to behave exactly the same as the original BWK awk.") (license license:x11))) (define-public python-bcbio-gff (package (name "python-bcbio-gff") (version "0.6.9") (source (origin (method url-fetch) (uri (pypi-uri "bcbio-gff" version)) (sha256 (base32 "1pm1szyxabhn8jismrj9cjhf88ajgcmm39f0cgf36iagw5qakprl")))) (build-system pyproject-build-system) (propagated-inputs (list python-biopython python-six)) (native-inputs (list python-pytest)) (home-page "https://github.com/chapmanb/bcbb/tree/master/gff") (synopsis "Read and write GFF files with Biopython integration") (description "This package lets you read and write files in Generic Feature Format (GFF) with Biopython integration.") (license (license:non-copyleft "http://www.biopython.org/DIST/LICENSE")))) (define-public python-bcbio-gff/biopython-1.73 (hidden-package (package (inherit python-bcbio-gff) (propagated-inputs (modify-inputs (package-propagated-inputs python-bcbio-gff) (replace "python-biopython" python-biopython-1.73)))))) ;; Note: the name on PyPi is "biofluff". (define-public python-biofluff (package (name "python-biofluff") (version "3.0.4") ;; PyPi tarball does not contain test data. (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/simonvh/fluff") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "12yvhgp72s2ygf3h07rrc852zd6q8swc41hm28mcczpsyprggxyz")))) (build-system pyproject-build-system) (arguments (list #:test-flags ;; Theses tests require internet access '(list "--ignore=tests/test_mirror.py" "-k" "not test_plots_big") #:phases '(modify-phases %standard-phases (add-after 'unpack 'matplotlib-compatibility (lambda _ (substitute* "fluff/plot.py" (("beginarrow=False, endarrow=True,") ""))))))) (propagated-inputs (list htseq python-matplotlib python-numpy python-palettable python-pybedtools python-pybigwig python-pysam python-scikit-learn python-scipy)) (native-inputs (list python-pytest)) (home-page "https://github.com/simonvh/fluff/") (synopsis "Analysis and visualization of high-throughput sequencing data") (description "Fluff is a Python package that contains several scripts to produce pretty, publication-quality figures for next-generation sequencing experiments.") (license license:expat))) (define-public python-bulkvis (let ((commit "00a82a90c7e748a34af896e779d27e78a2c82b5e") (revision "2")) (package (name "python-bulkvis") (version (git-version "2.0.0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/LooseLab/bulkVis") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "02blai158xyyqcg0ljzkmfa6ci05m4awrl4njvp9nwfp717xq8n0")) (modules '((guix build utils))) (snippet '(substitute* '("requirements.txt" "setup.py") (("tqdm~=4.46.1") "tqdm") (("tornado~=6.0.4") "tornado") (("pandas~=1.0.5") "pandas") (("h5py~=2.10.0") "h5py") ;; See below for com (("bokeh~=2.1.0") "bokeh"))))) (build-system pyproject-build-system) (arguments (list #:tests? #f ;There are no tests #:phases '(modify-phases %standard-phases ;; See https://github.com/LooseLab/bulkvis/issues/58 (add-after 'unpack 'bokeh-compatibility (lambda _ (substitute* "bulkvis/bulkvis.py" (("import importlib" m) (string-append m " from bokeh.command.subcommand import Argument from bokeh.util.dataclasses import entries\n")) (("( *)_parser.add_argument" m indent) (string-append (string-join (list "if isinstance(opts, Argument):\n" " opts = dict(entries(opts))\n") indent 'prefix) m)))))))) (propagated-inputs (list python-bokeh python-dill python-h5py python-joblib python-matplotlib python-numpy python-pandas python-plotly python-readpaf python-scikit-learn python-scikit-image python-scipy python-seaborn python-tornado-6 python-tqdm python-umap-learn)) (native-inputs (list python-pytest)) (home-page "https://github.com/LooseLab/bulkVis") (synopsis "Interactive visualization of bulk RNA-seq data") (description "This is a Python package for the interactive visualization of bulk RNA-seq data. It provides a range of plotting functions and interactive tools to explore and analyze bulk RNA-seq data.") (license license:expat)))) (define-public python-cell2cell (package (name "python-cell2cell") (version "0.6.8") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/earmingol/cell2cell") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "1hwww0rcv8sc4k312n4d0jhbyix1jjqgv5djg25bw8127q5iym3s")) (modules '((guix build utils))) (snippet '(begin ;; We remove the dependency on statannotations because it ;; will not work with the current version of seaborn. See ;; https://github.com/trevismd/statannotations/issues/122 (substitute* "cell2cell/plotting/factor_plot.py" (("from statannotations.Annotator import Annotator") "") (("if statistical_test is not None") "if False")) (substitute* "setup.py" (("'statannotations',") "") ;; We provide version 1.0.4, which should be fine. (("'gseapy == 1.0.3'") "'gseapy'") ;; Using matplotlib 3.5.2 leads to this bug: ;; https://github.com/earmingol/cell2cell/issues/19 but we ;; can't package a different minor version of matplotlib ;; and limit its use to just this package. (("matplotlib >= 3.2.0,<=3.5.1") "")))))) (build-system pyproject-build-system) (arguments (list #:tests? #f ;There are no tests #:phases '(modify-phases %standard-phases ;; Numba needs a writable dir to cache functions. (add-before 'build 'set-numba-cache-dir (lambda _ (setenv "NUMBA_CACHE_DIR" "/tmp")))))) (propagated-inputs (list python-gseapy python-kneed python-matplotlib python-networkx python-numpy python-openpyxl python-pandas python-scikit-learn python-scipy python-seaborn python-statsmodels python-scanpy python-seaborn python-tensorly python-tqdm python-umap-learn python-xlrd)) (home-page "https://github.com/earmingol/cell2cell") (synopsis "Python library for cell communication analysis") (description "Cell2cell is a Python library for cell communication analysis. This is a method to calculate, visualize and analyze communication between cell types. Cell2cell is suitable for single-cell RNA sequencing (scRNA-seq) data.") (license license:bsd-3))) (define-public python-cellbender (package (name "python-cellbender") (version "0.2.2") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/broadinstitute/CellBender") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "0h9d9pznffdbya631hkk7b7jwjrgx5saqssar1d42qbyvdji3hgy")))) (build-system pyproject-build-system) (arguments (list #:tests? #false)) ;there are none (propagated-inputs (list python-anndata python-matplotlib python-numpy python-pandas python-pyro-ppl python-scikit-learn python-scipy python-sphinx python-sphinx-argparse python-sphinx-autodoc-typehints python-sphinx-rtd-theme python-sphinxcontrib-programoutput python-tables)) (home-page "https://cellbender.rtfd.io/") (synopsis "Eliminate technical artifacts from single-cell RNA-seq data") (description "CellBender is a software package for eliminating technical artifacts from high-throughput single-cell RNA sequencing (scRNA-seq) data.") (license license:bsd-3))) (define-public python-celltypist (package (name "python-celltypist") (version "1.6.2") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/Teichlab/celltypist") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "0c42cx01zkxr0dk5f1d7q71qdi18v2smlc3wpvwyjlzplya7k2iy")))) (build-system pyproject-build-system) (arguments (list #:tests? #false ;there are none #:phases '(modify-phases %standard-phases (add-before 'check 'set-home ;; The sanity check requires a HOME directory, because celltypist ;; wants to write settings. (lambda _ (setenv "HOME" "/tmp"))) ;; Numba needs a writable dir to cache functions. (add-before 'build 'set-numba-cache-dir (lambda _ (setenv "NUMBA_CACHE_DIR" "/tmp")))))) (propagated-inputs (list python-click python-leidenalg python-numpy python-openpyxl python-pandas python-scanpy python-scikit-learn python-requests)) (home-page "https://github.com/Teichlab/celltypist") (synopsis "Tool for semi-automatic cell type classification") (description "CellTypist is an automated cell type annotation tool for scRNA-seq datasets on the basis of logistic regression classifiers optimised by the stochastic gradient descent algorithm. CellTypist allows for cell prediction using either built-in (with a current focus on immune sub-populations) or custom models, in order to assist in the accurate classification of different cell types and subtypes.") (license license:expat))) (define-public python-cmseq (package (name "python-cmseq") (version "1.0.4") (source (origin (method url-fetch) (uri (pypi-uri "CMSeq" version)) (sha256 (base32 "0p6a99c299m5wi2z57dgqz52m1z3nfr8mv7kdnk2jvl2p9nql0wk")))) (build-system pyproject-build-system) (arguments (list #:tests? #false ;there are no tests #:phases '(modify-phases %standard-phases (add-after 'unpack 'patch-samtools-reference (lambda* (#:key inputs #:allow-other-keys) (substitute* "cmseq/cmseq.py" (("'samtools'") (string-append "'" (search-input-file inputs "/bin/samtools") "'")))))))) (inputs (list samtools)) (propagated-inputs (list python-bcbio-gff/biopython-1.73 python-biopython-1.73 python-numpy python-pandas python-pysam python-scipy)) (home-page "https://github.com/SegataLab/cmseq/") (synopsis "Set of utilities on sequences and BAM files") (description "CMSeq is a set of commands to provide an interface to .bam files for coverage and sequence consensus.") (license license:expat))) (define-public python-cyvcf2 (package (name "python-cyvcf2") (version "0.30.28") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/brentp/cyvcf2") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "16yhfax509zyip8kkq2b0lflx5bdq5why7d785ayrqyzzq2rxqkk")) (modules '((guix build utils))) (snippet ;; Delete bundled library '(delete-file-recursively "htslib")))) (build-system pyproject-build-system) (arguments (list #:phases #~(modify-phases %standard-phases (add-before 'check 'build-extensions (lambda _ ;; Cython extensions have to be built before running the tests. (invoke "python" "setup.py" "build_ext" "--inplace"))) (add-after 'unpack 'fix-setup (lambda* (#:key inputs #:allow-other-keys) (substitute* "setup.py" (("^htslib_include_dirs =.*") (string-append "htslib_include_dirs = [\"" #$(this-package-input "htslib") "/include\"]\n")) (("lib_name = \"libhts.so\"") (string-append "lib_name = \"" (search-input-file inputs "lib/libhts.so.3") "\"\n"))))) (add-before 'build 'use-system-htslib-package (lambda _ (setenv "CYTHONIZE" "1") (setenv "CYVCF2_HTSLIB_MODE" "EXTERNAL")))))) (inputs (list curl htslib libdeflate openssl zlib)) (native-inputs (list python-cython python-pytest)) (propagated-inputs (list python-click python-coloredlogs python-numpy)) (home-page "https://github.com/brentp/cyvcf2/") (synopsis "Fast vcf file parsing with Cython and htslib") (description "Cyvcf2 is a Cython wrapper around htslib built for fast parsing of Variant Call Format (VCF) files.") (license license:expat))) (define-public python-decoupler-py (package (name "python-decoupler-py") (version "1.6.0") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/saezlab/decoupler-py") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "1mqkp0i8k5hzhfnka4nc2f0phmrs0k404ynbl1lqfjzywx25y75h")))) (build-system pyproject-build-system) (arguments (list #:test-flags '(list "-k" ;; These tests require internet access (string-append "not test_get_resource" " and not test_show_resources" " and not test_get_dorothea" " and not test_get_progeny" " and not test_get_ksn_omnipath" ;; This attempts to download things for Omnipath " and not test_get_collectri")) #:phases '(modify-phases %standard-phases (add-before 'check 'set-home ;; Some tests require a home directory to be set. (lambda _ (setenv "HOME" "/tmp"))) ;; Numba needs a writable dir to cache functions. (add-before 'build 'set-numba-cache-dir (lambda _ (setenv "NUMBA_CACHE_DIR" "/tmp")))))) (propagated-inputs (list python-adjusttext python-anndata python-ipython python-matplotlib python-nbsphinx python-numba python-numpy python-numpydoc python-omnipath python-scanpy python-scikit-learn python-scipy python-skranger python-tqdm python-typing-extensions)) (native-inputs (list python-pytest)) (home-page "https://github.com/saezlab/decoupler-py") (synopsis "Framework for modeling, analyzing and interpreting single-cell RNA-seq data") (description "This package provides different statistical methods to extract biological activities from omics data within a unified framework.") (license license:gpl3+))) (define-public python-demuxem (package (name "python-demuxem") (version "0.1.7") (source (origin (method url-fetch) (uri (pypi-uri "demuxEM" version)) (sha256 (base32 "1bhyxqjk44bmyd26m1smapf68wyf7252kk65i27k50dd3kswgnd6")))) (build-system pyproject-build-system) ;; There are no tests. (arguments (list #:tests? #false)) (propagated-inputs (list python-docopt python-importlib-metadata python-numpy python-pandas python-pegasusio python-scikit-learn python-scipy python-seaborn)) (native-inputs (list python-cython python-setuptools-scm)) (home-page "https://github.com/lilab-bcb/demuxEM") (synopsis "Analyze cell-hashing/nucleus-hashing data") (description "This is a Python module for analyzing cell-hashing/nucleus-hashing data. It is the demultiplexing module of Pegasus, which is used by Cumulus in the demultiplexing step.") (license license:bsd-3))) (define-public python-doubletdetection (package (name "python-doubletdetection") (version "4.2") (source (origin (method url-fetch) (uri (pypi-uri "doubletdetection" version)) (sha256 (base32 "0v0a19014h4p6x8pyz1s78xn3q5w5166cysvg574z6vw79a3s9vp")))) (build-system pyproject-build-system) (arguments (list #:tests? #false ;there are none #:phases #~(modify-phases %standard-phases (add-after 'unpack 'use-poetry-core (lambda _ ;; Patch to use the core poetry API. (substitute* "pyproject.toml" (("poetry.masonry.api") "poetry.core.masonry.api"))))))) (propagated-inputs (list python-anndata python-ipywidgets python-leidenalg python-vtraag-louvain python-matplotlib python-numpy python-pandas python-phenograph python-scanpy python-scipy python-tqdm)) (native-inputs (list python-black python-flake8 python-poetry-core python-pytest)) (home-page "https://github.com/JonathanShor/DoubletDetection") (synopsis "This is a package to detect doublets in single-cell RNA-seq count matrices") (description "This package provides a method to detect and enable removal of doublets from single-cell RNA-sequencing.") (license license:expat))) (define-public python-hclust2 (package (name "python-hclust2") (version "1.0.0") (source (origin (method url-fetch) (uri (pypi-uri "hclust2" version)) (sha256 (base32 "0v89n2g42d7jhgfs8glf06apgxx6aswp3mfisgnhm518cv8z2rwn")))) (build-system pyproject-build-system) (arguments (list #:tests? #f)) ;there are no tests (propagated-inputs (list python-matplotlib python-numpy python-pandas python-scipy)) (home-page "https://github.com/SegataLab/hclust2/") (synopsis "Plotting heat-maps for publications") (description "Hclust2 is a handy tool for plotting heat-maps with several useful options to produce high quality figures that can be used in publications.") (license license:expat))) (define-public python-htsget (package (name "python-htsget") (version "0.2.6") (source (origin (method url-fetch) (uri (pypi-uri "htsget" version)) (sha256 (base32 "111q4pzkav26aa3hkgh948wqlyrq7dq6sjml9z63n3blw8s6b0c4")))) (build-system pyproject-build-system) (native-inputs (list python-setuptools-scm)) (propagated-inputs (list python-humanize python-requests python-six)) (home-page "https://pypi.org/project/htsget/") (synopsis "Python API and command line interface for the GA4GH htsget API") (description "This package is a client implementation of the GA4GH htsget protocol. It provides a simple and reliable way to retrieve genomic data from servers supporting the protocol.") (license license:asl2.0))) (define-public python-liana-py (package (name "python-liana-py") (version "1.1.0") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/saezlab/liana-py") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "0f5al0v55haja91q9gd409v7q78mmp1wv9znsplsbjp6lfspjfnw")))) (build-system pyproject-build-system) (arguments (list #:test-flags '(list "-k" ;; These tests require internet access. (string-append "not test_generate_lr_resource" " and not test_get_metalinks" " and not test_get_metalinks_values" " and not test_describe_metalinks" " and not test_generate_nondefault_lr_resource" ;; Minor accuracy difference " and not test_bivar_morans_perms" ;; XXX unclear failure: 'coo_matrix' object is not ;; subscriptable " and not test_bivar_product" ) ;; These need the optional squidpy, which we don't have yet. "--ignore=liana/tests/test_misty.py" ;; These need the optional corneto. "--ignore=liana/tests/test_causalnet.py") #:phases '(modify-phases %standard-phases (add-after 'unpack 'relax-requirements (lambda _ ;; Don't fail the sanity check when these optional inputs aren't ;; available. (substitute* "pyproject.toml" (("^pre-commit =.*") "")))) ;; Numba needs a writable directory to cache functions. (add-before 'build 'set-numba-cache-dir (lambda _ (setenv "NUMBA_CACHE_DIR" "/tmp")))))) (propagated-inputs (list python-anndata python-cell2cell python-decoupler-py python-hypothesis python-ipykernel python-ipython python-mudata python-nbconvert python-nbsphinx python-numpy python-numpydoc python-omnipath python-pandas python-plotnine python-pypandoc python-scipy python-requests python-scanpy python-statsmodels python-tqdm tzdata)) (native-inputs (list python-black python-poetry-core python-pytest python-pytest-cov)) (home-page "https://github.com/saezlab/liana-py") (synopsis "LIANA is a ligand-receptor analysis framework") (description "This is a Ligand-Receptor inference framework. The framework enables the use of any LR method with any resources.") (license license:gpl3+))) (define-public python-logomaker (package (name "python-logomaker") (version "0.8") (source (origin (method url-fetch) (uri (pypi-uri "logomaker" version)) (sha256 (base32 "0v9z3ml1s7imk28hqyhrqjqg3sq0j29lx975d36n2ybdgld51iyq")))) (build-system pyproject-build-system) (propagated-inputs (list python-matplotlib python-numpy python-pandas)) (home-page "https://logomaker.readthedocs.io") (synopsis "Package for making Sequence Logos") (description "Logomaker is a Python package for generating publication-quality sequence logos. Logomaker can generate both standard and highly customized logos illustrating the properties of DNA, RNA, or protein sequences. Logos are rendered as vector graphics embedded within native matplotlib Axes objects, making them easy to style and incorporate into multi-panel figures.") (license license:expat))) (define-public python-magic-impute (package (name "python-magic-impute") (version "1.2.1") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/KrishnaswamyLab/MAGIC") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "1yjs16vg87lcg9g16bnblg1v9sk73j6dm229lkcz0bfjlzxjhv8w")))) (build-system pyproject-build-system) (arguments (list #:tests? #false ;there are none #:phases '(modify-phases %standard-phases (add-after 'unpack 'chdir (lambda _ (chdir "python")))))) (propagated-inputs (list python-future python-graphtools python-matplotlib python-numpy python-pandas python-scikit-learn python-scipy python-tasklogger)) (home-page "https://github.com/KrishnaswamyLab/MAGIC") (synopsis "Markov affinity-based graph imputation of cells") (description "MAGIC is an interactive tool to impute missing values in single-cell sequencing data and to restore the structure of the data. It also provides data pre-processing functionality such as dimensionality reduction and gene expression visualization.") (license license:gpl2+))) (define-public python-metacells (package (name "python-metacells") (version "0.9.4") (source (origin (method url-fetch) (uri (pypi-uri "metacells" version)) (sha256 (base32 "02f63nxz6b60vl6s4n9vapaysnq1w5f3x7c179rh2rr7j2k5cf1y")))) #; (properties '((tunable? . #t))) (build-system pyproject-build-system) (arguments (list #:phases #~(modify-phases %standard-phases ;; The package "python-igraph" has been deprecated in favor of ;; just "igraph". (add-after 'unpack 'rename-igraph (lambda _ (substitute* "requirements.txt" (("python-igraph") "igraph")))) (add-after 'unpack 'do-not-tune (lambda _ ;; Without this they pass -march=native to the compiler. (setenv "WHEEL" "1"))) ;; Numba needs a writable dir to cache functions. (add-before 'check 'set-numba-cache-dir (lambda _ (setenv "NUMBA_CACHE_DIR" "/tmp"))) (add-before 'build 'build-extensions (lambda _ (invoke "python" "setup.py" "build_ext" "--inplace")))))) (propagated-inputs (list python-anndata python-cvxpy python-fastcluster python-importlib-metadata python-numpy python-pandas python-psutil python-igraph python-pyyaml python-scanpy python-scipy python-threadpoolctl python-umap-learn)) (native-inputs (list python-black python-bumpversion python-flake8 python-isort python-mypy python-mypy-extensions python-pylint python-pytest python-pytest-cov python-sphinx python-sphinx-rtd-theme python-tox python-twine)) (home-page "https://github.com/tanaylab/metacells.git") (synopsis "Single-cell RNA Sequencing Analysis") (description "The metacells package implements the improved metacell algorithm for single-cell RNA sequencing (scRNA-seq) data analysis within the scipy framework, and projection algorithm based on it. The original metacell algorithm was implemented in R. The Python package contains various algorithmic improvements and is scalable for larger data sets (millions of cells).") (license license:expat))) (define-public python-parabam (package (name "python-parabam") (version "3.0.1") (source (origin (method url-fetch) (uri (pypi-uri "parabam" version)) (sha256 (base32 "1cy9q3gzdawi1kilycpd7waymjmrwsg8czwycfp13g301ir9xyp3")) (modules '((guix build utils))) (snippet '(substitute* "setup.py" (("'argparse',") ""))))) (build-system pyproject-build-system) (propagated-inputs (list python-numpy python-pysam)) (home-page "https://github.com/cancerit/parabam") (synopsis "Parallel BAM File Analysis") (description "Parabam is a tool for processing sequencing files in parallel. It uses Python's native multiprocessing framework to apply a user defined rule on an input file.") (license license:gpl3))) (define-public python-pdbfixer (package (name "python-pdbfixer") (version "1.9") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/openmm/pdbfixer") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "1zjhb19q5dclkwvzh8n29p31n1vzkhlmmzwqllimi89jsis1cx35")))) (build-system pyproject-build-system) (arguments (list #:test-flags '(list "-k" ;; These tests fail because they require internet access. (string-append "not test_build_and_simulate.py" " and not test_cli.py" " and not test_mutate.py")))) (propagated-inputs (list openmm python-numpy)) (native-inputs (list python-pytest)) (home-page "https://github.com/openmm/pdbfixer") (synopsis "Application for fixing problems in Protein Data Bank") (description "PDBFixer is designed to rectify issues in Protein Data Bank files. Its intuitive interface simplifies the process of resolving problems encountered in PDB files prior to simulation tasks.") (license license:expat))) (define-public python-peaks2utr (package (name "python-peaks2utr") (version "1.2.0") (source (origin (method url-fetch) (uri (pypi-uri "peaks2utr" version)) (sha256 (base32 "1idp9cgwqxvryf4qqrc1xjsamfqn3jmr56kmjp2h1ysmckwmhw4v")))) (build-system pyproject-build-system) (arguments (list #:test-flags ;; These two tests fail because file names are not URLs. '(list "-k" "not test_annotation.py"))) (propagated-inputs (list python-asgiref python-gffutils python-importlib-resources macs python-numpy python-psutil python-pybedtools python-pysam python-requests python-tqdm python-typing-extensions python-zipp)) (home-page "https://github.com/haessar/peaks2utr") (synopsis "Python CLI for annotating three prime UTR") (description "This package provides a robust, parallelized Python CLI for annotating three prime UTR.") (license license:gpl3+))) (define-public python-pegasusio (package (name "python-pegasusio") (version "0.7.1") (source (origin (method url-fetch) (uri (pypi-uri "pegasusio" version)) (sha256 (base32 "0gqygspdy398vjymdy6756jmk99s7fhwav9rivdx59kpqjcdxaz9")))) (build-system pyproject-build-system) ;; There are no tests. (arguments (list #:tests? #false)) (propagated-inputs (list python-anndata python-docopt python-h5py python-importlib-metadata python-loompy python-natsort python-numpy python-pandas python-pillow python-scipy python-zarr)) (native-inputs (list python-cython python-setuptools-scm)) (home-page "https://github.com/lilab-bcb/pegasusio") (synopsis "Read or write single-cell genomics data") (description "Pegasusio is a Python package for reading or writing single-cell genomics data.") (license license:bsd-3))) (define-public python-phenograph (package (name "python-phenograph") (version "1.5.7") (source (origin (method url-fetch) (uri (pypi-uri "PhenoGraph" version)) (sha256 (base32 "0nji449mzwgp1f87iknl5fmnjdkrhkfkapxvafxdw01s0jg8zcj6")) (modules '((guix build utils))) ;; Remove bundled binaries (snippet '(delete-file-recursively "phenograph/louvain")))) (build-system pyproject-build-system) (arguments (list #:phases #~(modify-phases %standard-phases ;; This test can never succeed because Q_leiden is never set to ;; anything other than None. (add-after 'unpack 'disable-leiden-test (lambda _ (substitute* "tests/test_cluster.py" (("def test_run_leiden") "def _test_run_leiden")))) (add-after 'unpack 'patch-louvain (lambda* (#:key inputs #:allow-other-keys) (substitute* "phenograph/core.py" (("lpath = os.path.*") (string-append "lpath = \"" (dirname (search-input-file inputs "/bin/community")) "\"\n")) (("linux-(community|hierarchy|convert)" _ thing) thing) ;; Do not write binaries, because the unmodified "convert" ;; from louvain only knows how to process plain text files. (("with open\$filename \\+ \".bin\", \"w\\+b\"\$ as f:") "with open(filename + \".bin\", \"w+\") as f:") (("f.writelines\$\\[e for t in zip\\(ij, s\$ for e in t\\]\\)") "for [src, dest], weight in zip(ij, s): \ f.write(src.astype(\"str\") + ' ' + \ dest.astype(\"str\") + ' ' + \ weight.astype(\"str\") + '\\n')"))))))) (inputs (list louvain)) (propagated-inputs (list python-leidenalg python-numpy python-psutil python-scikit-learn python-scipy)) (native-inputs (list python-pytest)) (home-page "https://github.com/dpeerlab/PhenoGraph.git") (synopsis "Graph-based clustering for high-dimensional single-cell data") (description "PhenoGraph is a clustering method designed for high-dimensional single-cell data. It works by creating a graph representing phenotypic similarities between cells and then identifying communities in this graph.") (license license:expat))) (define-public python-phylophlan (package (name "python-phylophlan") (version "3.0.3") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/biobakery/phylophlan") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "1wz70xzxqx2sf5flmf45m15jq027dqijfaj1r51pl50w5x6dkawx")))) (build-system pyproject-build-system) (arguments (list #:tests? #f)) ;there are no tests (propagated-inputs (list python-biopython python-dendropy python-matplotlib python-numpy python-pandas python-seaborn)) (home-page "https://github.com/biobakery/phylophlan") (synopsis "Phylogenetic analysis of microbial isolates and genomes from metagenomes") (description "This package is an integrated pipeline for large-scale phylogenetic profiling of genomes and metagenomes. PhyloPhlAn is an accurate, rapid, and easy-to-use method for large-scale microbial genome characterization and phylogenetic analysis at multiple levels of resolution. This software package can assign both genomes and @acronym{MAGs, metagenome-assembled genomes} to @acronym{SGBs, species-level genome bins}. PhyloPhlAn can reconstruct strain-level phylogenies using clade- specific maximally informative phylogenetic markers, and can also scale to very large phylogenies comprising >17,000 microbial species.") (license license:expat))) (define-public python-pybedtools (package (name "python-pybedtools") (version "0.9.0") (source (origin (method url-fetch) (uri (pypi-uri "pybedtools" version)) (sha256 (base32 "18rhzk08d3rpxhi5xh6pqg64x6v5q3daw6y3v54k85v4swncjrwj")))) (build-system pyproject-build-system) (arguments `(#:modules ((srfi srfi-26) (guix build utils) (guix build python-build-system) (guix build pyproject-build-system)) ;; See https://github.com/daler/pybedtools/issues/192 #:phases (modify-phases %standard-phases (add-after 'unpack 'disable-broken-tests (lambda _ (substitute* "pybedtools/test/test_helpers.py" ;; Requires internet access. (("def test_chromsizes") "def _do_not_test_chromsizes") ;; Broken as a result of the workaround used in the check phase ;; (see: https://github.com/daler/pybedtools/issues/192). (("def test_getting_example_beds") "def _do_not_test_getting_example_beds")) ;; This issue still occurs on python2 (substitute* "pybedtools/test/test_issues.py" (("def test_issue_303") "def _test_issue_303")))) ;; Force the Cythonization of C++ files to guard against compilation ;; problems. (add-after 'unpack 'remove-cython-generated-files (lambda _ (let ((cython-sources (map (cut string-drop-right <> 4) (find-files "." "\\.pyx$"))) (c/c++-files (find-files "." "\\.(c|cpp|cxx)$"))) (define (strip-extension filename) (string-take filename (string-index-right filename #\.))) (define (cythonized? c/c++-file) (member (strip-extension c/c++-file) cython-sources)) (for-each delete-file (filter cythonized? c/c++-files))))) (add-after 'remove-cython-generated-files 'generate-cython-extensions (lambda _ (invoke "python" "setup.py" "cythonize"))) (replace 'check (lambda _ ;; The tests need to be run from elsewhere... (mkdir-p "/tmp/test") (copy-recursively "pybedtools/test" "/tmp/test") (with-directory-excursion "/tmp/test" (invoke "pytest" "-v" "--doctest-modules"))))))) (propagated-inputs (list bedtools samtools python-matplotlib python-pysam python-pyyaml)) (native-inputs (list python-numpy python-pandas python-cython kentutils ; for bedGraphToBigWig python-six ;; For the test suite. python-pytest python-psutil)) (home-page "https://pythonhosted.org/pybedtools/") (synopsis "Python wrapper for BEDtools programs") (description "This package is a Python wrapper for Aaron Quinlan's BEDtools programs, which are widely used for genomic interval manipulation or \"genome algebra\". pybedtools extends BEDTools by offering feature-level manipulations from with Python.") ;; pypi lists GPLv2 in the PKG-INFO and website, but was relicensed in ;; version 0.9.0 and the LICENSE.txt is consistent with the source code. ;; ;; pybedtools/include/gzstream.cpp and pybedtools/include/gzstream.h are ;; licensed lgpl2.1+ (license (list license:expat license:lgpl2.1+)))) (define-public python-ega-download-client (package (name "python-ega-download-client") (version "5.1.0") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/EGA-archive/ega-download-client") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "0k9rfq2yyvfxs5sq9lsm8krp9ddx4s18hv85ikf3b37zv24kpwjk")))) (build-system pyproject-build-system) (arguments (list #:test-flags '(list ;; These tests fail because they require internet access. "--ignore=tests/functional/test_download.py" "--ignore=tests/functional/test_htsget.py" "-k" (string-append "not test_error_5xx" " and not test_error_too_many_requests" ;; Something's wrong here. On some powerful machines ;; (but not on my laptop) these fail, and tests like ;; test_file_is_saved_into_an_existing_directory_which_was_specified_by_the_user ;; take a *very* long time to complete. ;; ;; It looks like "dataset_in_fire.download" takes an ;; unusually long time on those machines. We disable ;; tests that fail under these conditions. " and not test_download_file" " and not test_output_file_is_removed_if_md5_was_invalid" " and not test_post_stats_if_download_succeeded")) #:phases '(modify-phases %standard-phases (add-after 'unpack 'relax-requirements (lambda _ (substitute* "setup.py" (("==") ">="))))))) (propagated-inputs (list python-htsget python-psutil python-requests python-tqdm python-urllib3)) (native-inputs (list python-coverage python-pytest python-pyfakefs python-responses python-mock)) (home-page "https://github.com/EGA-archive/ega-download-client") (synopsis "EGA download client") (description "PyEGA3 is a tool for viewing and downloading files from authorized EGA datasets. It uses the EGA data API and has several key features: @itemize @item Files are transferred over secure https connections and received unencrypted, so no need for decryption after download. @item Downloads resume from where they left off in the event that the connection is interrupted. @item Supports file segmenting and parallelized download of segments, improving overall performance. @item After download completes, file integrity is verified using checksums. @item Implements the GA4GH-compliant htsget protocol for download of genomic ranges for data files with accompanying index files. @end itemize\n") (license license:asl2.0))) (define-public python-scdamandtools (package (name "python-scdamandtools") (version "1.0") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/KindLab/scDamAndTools") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "1mblw6cn5jqik6ky8cv7ry99z6jm1i4r71pzdfl398vrwbda65gd")))) (build-system pyproject-build-system) (arguments (list #:tests? #f)) ;there are none (propagated-inputs (list python-h5py python-numpy python-sortedcontainers python-pandas python-pysam python-tqdm)) (native-inputs (list python-cython python-pytest)) (home-page "https://github.com/KindLab/scDamAndTools") (synopsis "Functions for processing raw scDam&T-seq data") (description "This is a set of functions for processing raw scDam&T-seq data. scDam&T-seq is a method to simultaneously measure protein-DNA interactions and transcription from single cells (Rooijers et al., 2019). It combines a DamID-based method to measure protein-DNA interactions and an adaptation of CEL-Seq to measure transcription. The starting point of the workflow is raw sequencing data and the end result are tables of UMI-unique DamID and CEL-Seq counts.") (license license:expat))) (define-public python-snaptools (package (name "python-snaptools") (version "1.4.8") (source (origin (method url-fetch) (uri (pypi-uri "snaptools" version)) (sha256 (base32 "1s5373g5jjbshh3q39zy7dlxr7nda6ksxq9d1gw46h82c4fsmfbn")))) (build-system pyproject-build-system) (arguments (list #:tests? #false)) ;there are none (propagated-inputs (list python-future python-h5py python-louvain python-numpy python-pybedtools python-pysam)) (home-page "https://github.com/r3fang/SnapTools") (synopsis "Tools for processing snap files" ) (description "@code{SnapTools} can operate on snap files the following types of operations: @itemize @item index the reference genome before alignment; @item align reads to the corresponding reference genome; @item pre-process by convert pair-end reads into fragments, checking the mapping quality score, alingment and filtration; @item create the cell-by-bin matrix. @end itemize") (license license:asl2.0))) (define-public python-telomerecat (package (name "python-telomerecat") (version "4.0.2") (source (origin (method url-fetch) (uri (pypi-uri "telomerecat" version)) (sha256 (base32 "16mfdqmp0j6g3h26h59334w9lqb4qihqrlzwvgznj0fiqs1rkxn2")))) (build-system pyproject-build-system) (arguments (list #:tests? #false)) ;there are none (propagated-inputs (list python-click python-numpy python-pandas python-parabam python-pysam)) (home-page "https://github.com/cancerit/telomerecat") (synopsis "Telomere computational analysis tool") (description "Telomerecat is a tool for estimating the average telomere length (TL) for a paired end, whole genome sequencing (WGS) sample. Telomerecat is adaptable, accurate and fast. The algorithm accounts for sequencing amplification artifacts, anneouploidy (common in cancer samples) and noise generated by WGS. For a high coverage WGS BAM file of around 100GB telomerecat can produce an estimate in ~1 hour.") (license license:gpl3))) (define-public python-bioframe (package (name "python-bioframe") (version "0.6.4") (source (origin (method git-fetch) ;; pypi version does not contain tests and requirements.txt (uri (git-reference (url "https://github.com/open2c/bioframe") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "1m99hgxw4cb2x4qszb2lhp1isz57sdkqbmcgisnbqxqxkv4gba7v")))) (build-system pyproject-build-system) (arguments (list #:test-flags '(list "-k" (string-append "not test_fetch_chromsizes" " and not test_fetch_chromsizes_local_vs_ucsc" " and not test_fetch_centromeres")) #:phases '(modify-phases %standard-phases (add-before 'check 'pre-check (lambda _ (setenv "MPLCONFIGDIR" "/tmp")))))) (native-inputs (list python-biopython python-hatchling python-pysam python-pytest python-wheel)) (propagated-inputs (list python-matplotlib python-numpy python-pandas python-pyyaml python-requests)) (home-page "https://github.com/open2c/bioframe") (synopsis "Pandas utilities for tab-delimited and other genomic files") (description "This package is a library to enable flexible and scalable operations on genomic interval dataframes in Python. Bioframe enables access to a rich set of dataframe operations. Working in Python enables rapid visualization and iteration of genomic analyses. The philosophy underlying bioframe is to enable flexible operations. Instead of creating a function for every possible use-case, we encourage users to compose functions to achieve their goals.") (license license:expat))) (define-public python-biom-format (package (name "python-biom-format") (version "2.1.12") (source (origin (method git-fetch) ;; Use GitHub as source because PyPI distribution does not contain ;; test data: https://github.com/biocore/biom-format/issues/693 (uri (git-reference (url "https://github.com/biocore/biom-format") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "06x2d8fv80jp86kd66fm3ragmxrpa2j0lzsbm337ziqjnpsdwc0f")) (modules '((guix build utils))) ;; Delete generated C files. (snippet '(for-each delete-file (find-files "." "\\.c"))))) (build-system python-build-system) (arguments (list #:phases '(modify-phases %standard-phases (add-after 'unpack 'use-cython (lambda _ (setenv "USE_CYTHON" "1"))) (add-after 'unpack 'pandas-compatibility (lambda _ (substitute* "biom/tests/test_table.py" (("import pandas.util.testing") "import pandas.testing")))) (add-after 'unpack 'disable-broken-tests (lambda _ (substitute* "biom/tests/test_util.py" (("^(.+)def test_biom_open_hdf5_no_h5py" m indent) (string-append indent "@npt.dec.skipif(True, msg='Guix')\n" m))) (substitute* "biom/tests/test_table.py" (("^(.+)def test_from_hdf5_issue_731" m indent) (string-append indent "@npt.dec.skipif(True, msg='Guix')\n" m)) ;; Unclear why this one fails. There is no backtrace. (("^(.+)def test_to_dataframe_is_sparse" m indent) (string-append indent "@npt.dec.skipif(True, msg='Guix')\n" m)) ;; These need skbio, but that neeeds biom-format. (("^(.+)def test_align_tree_intersect_obs" m indent) (string-append indent "@npt.dec.skipif(True, msg='Guix')\n" m)) (("^(.+)def test_align_tree_intersect_tips" m indent) (string-append indent "@npt.dec.skipif(True, msg='Guix')\n" m)) (("^(.+)def test_align_tree_sample" m indent) (string-append indent "@npt.dec.skipif(True, msg='Guix')\n" m)))))))) (propagated-inputs (list python-anndata python-click python-flake8 python-future python-h5py python-numpy python-pandas ;;python-scikit-bio ;mutually recursive dependency python-scipy)) (native-inputs (list python-cython python-pytest python-pytest-cov python-nose)) (home-page "https://www.biom-format.org") (synopsis "Biological Observation Matrix (BIOM) format utilities") (description "The BIOM file format is designed to be a general-use format for representing counts of observations e.g. operational taxonomic units, KEGG orthology groups or lipid types, in one or more biological samples e.g. microbiome samples, genomes, metagenomes.") (license license:bsd-3))) (define-public python-pairtools (package (name "python-pairtools") (version "1.0.2") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/open2c/pairtools") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "0xn4cg4jq3rfn42h8rfwg0k6xkvihjrv32gwldb9y0jp05lzw9cs")))) (build-system python-build-system) (arguments `(#:phases (modify-phases %standard-phases (add-after 'unpack 'fix-references (lambda _ (substitute* '("pairtools/cli/header.py" "pairtools/cli/merge.py" "pairtools/cli/sort.py") (("/bin/bash") (which "bash"))))) (replace 'check (lambda* (#:key tests? #:allow-other-keys) (when tests? (with-directory-excursion "/tmp" (invoke "pytest" "-v")))))))) (native-inputs (list python-cython python-pytest)) (propagated-inputs (list htslib ; for bgzip, looked up in PATH samtools ; looked up in PATH lz4 ; for lz4c python-bioframe python-click python-numpy python-pandas python-pysam python-pyyaml python-scipy)) (home-page "https://github.com/open2c/pairtools") (synopsis "Process mapped Hi-C data") (description "Pairtools is a simple and fast command-line framework to process sequencing data from a Hi-C experiment. Process pair-end sequence alignments and perform the following operations: @itemize @item detect ligation junctions (a.k.a. Hi-C pairs) in aligned paired-end sequences of Hi-C DNA molecules @item sort @code{.pairs} files for downstream analyses @item detect, tag and remove PCR/optical duplicates @item generate extensive statistics of Hi-C datasets @item select Hi-C pairs given flexibly defined criteria @item restore @code{.sam} alignments from Hi-C pairs. @end itemize ") (license license:expat))) (define-public python-readpaf (package (name "python-readpaf") (version "0.0.10") (source (origin (method url-fetch) (uri (pypi-uri "readpaf" version)) (sha256 (base32 "15m6ffks4zwpp1ycwk6n02py6mw2yh7qr0vhpc178b91gldr97ia")))) (build-system pyproject-build-system) (arguments (list #:tests? #false)) ;there are none (propagated-inputs (list python-pandas)) (home-page "https://github.com/alexomics/read-paf") (synopsis "Minimap2 PAF file reader") (description "This is a fast parser for minimap2 PAF (Pairwise mApping Format) files.") (license license:expat))) (define-public bioperl-minimal (package (name "bioperl-minimal") (version "1.7.0") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/bioperl/bioperl-live") (commit (string-append "release-" (string-map (lambda (c) (if (char=? c #\.) #\- c)) version))))) (file-name (git-file-name name version)) (sha256 (base32 "0wl8yvzcls59pwwk6m8ahy87pwg6nnibzy5cldbvmcwg2x2w7783")))) (build-system perl-build-system) (arguments (let ((transitive-inputs (map (compose package-name cadr) (delete-duplicates (concatenate (map (compose package-transitive-target-inputs cadr) (package-inputs this-package))))))) `(#:phases (modify-phases %standard-phases (add-after 'install 'wrap-programs (lambda* (#:key outputs #:allow-other-keys) ;; Make sure all executables in "bin" find the required Perl ;; modules at runtime. As the PERL5LIB variable contains also ;; the paths of native inputs, we pick the transitive target ;; inputs from %build-inputs. (let* ((out (assoc-ref outputs "out")) (bin (string-append out "/bin/")) (path (string-join (cons (string-append out "/lib/perl5/site_perl") (map (lambda (name) (assoc-ref %build-inputs name)) ',transitive-inputs)) ":"))) (for-each (lambda (file) (wrap-program file `("PERL5LIB" ":" prefix (,path)))) (find-files bin "\\.pl$"))))))))) (inputs (list bash-minimal perl-module-build perl-data-stag perl-libwww perl-uri)) (native-inputs (list perl-test-most)) (home-page "https://metacpan.org/release/BioPerl") (synopsis "Bioinformatics toolkit") (description "BioPerl is the product of a community effort to produce Perl code which is useful in biology. Examples include Sequence objects, Alignment objects and database searching objects. These objects not only do what they are advertised to do in the documentation, but they also interact - Alignment objects are made from the Sequence objects, Sequence objects have access to Annotation and SeqFeature objects and databases, Blast objects can be converted to Alignment objects, and so on. This means that the objects provide a coordinated and extensible framework to do computational biology.") (license license:perl-license))) (define-public perl-bio-db-hts (package (name "perl-bio-db-hts") (version "3.01") (source (origin (method url-fetch) (uri (string-append "mirror://cpan/authors/id/A/AV/AVULLO/Bio-DB-HTS-" version ".tar.gz")) (sha256 (base32 "0hjg0igfkpvh27zdkdr6pa7cqm9n6r7cwz0np74cl4wmawgvr9hj")))) (build-system perl-build-system) (native-inputs (list perl-module-build pkg-config)) (propagated-inputs (list bioperl-minimal htslib-1.9)) (home-page "https://metacpan.org/release/Bio-DB-HTS") (synopsis "Perl interface to HTS library for DNA sequencing") (description "This is a Perl interface to the HTS library for DNA sequencing.") (license license:asl2.0))) (define-public python-biopython (package (name "python-biopython") (version "1.80") (source (origin (method url-fetch) ;; use PyPi rather than biopython.org to ease updating (uri (pypi-uri "biopython" version)) (sha256 (base32 "0hqf3jsxn2sphcx81fx7x3i69sarpjsi70fzw98f8rw7z2d5x02j")))) (build-system pyproject-build-system) (arguments '(#:phases (modify-phases %standard-phases (add-before 'check 'set-home ;; Some tests require a home directory to be set. (lambda _ (setenv "HOME" "/tmp")))))) (propagated-inputs (list python-numpy)) (home-page "https://biopython.org/") (synopsis "Tools for biological computation in Python") (description "Biopython is a set of tools for biological computation including parsers for bioinformatics files into Python data structures; interfaces to common bioinformatics programs; a standard sequence class and tools for performing common operations on them; code to perform data classification; code for dealing with alignments; code making it easy to split up parallelizable tasks into separate processes; and more.") (license (license:non-copyleft "http://www.biopython.org/DIST/LICENSE")))) (define-public python-biopython-1.73 (package (inherit python-biopython) (version "1.73") (source (origin (method url-fetch) ;; use PyPi rather than biopython.org to ease updating (uri (pypi-uri "biopython" version)) (sha256 (base32 "1q55jhf76z3k6is3psis0ckbki7df26x7dikpcc3vhk1vhkwribh")))))) (define-public python-fastalite (package (name "python-fastalite") (version "0.3") (source (origin (method url-fetch) (uri (pypi-uri "fastalite" version)) (sha256 (base32 "1qli6pxp77i9xn2wfciq2zaxhl82bdxb33cpzqzj1z25yd036wqj")))) (build-system python-build-system) (arguments `(#:tests? #f)) ; Test data is not distributed. (home-page "https://github.com/nhoffman/fastalite") (synopsis "Simplest possible FASTA parser") (description "This library implements a FASTA and a FASTQ parser without relying on a complex dependency tree.") (license license:expat))) (define-public biosoup (package (name "biosoup") (version "0.10.0") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/rvaser/biosoup") ;; Corresponds to version 0.10.0 (commit "38181f09854ff42cbd9632200a2ec9fb37a4b7b6"))) (file-name (git-file-name name version)) (sha256 (base32 "02hvyka703zagx0nvv2yx3dkc748zc8g6qbrpya7r8kfkcl7y8hw")))) (build-system cmake-build-system) (arguments `(#:phases (modify-phases %standard-phases (replace 'check (lambda* (#:key tests? #:allow-other-keys) (when tests? (invoke "./bin/biosoup_test"))))))) (native-inputs (list googletest)) (home-page "https://github.com/rvaser/biosoup") (synopsis "C++ support library for bioinformatics tools") (description "Biosoup is a C++ collection of header-only data structures used for storage and logging in bioinformatics tools.") (license license:expat))) (define-public bioparser (package (name "bioparser") (version "3.0.13") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/rvaser/bioparser") ;; Corresponds to tag 3.0.13 (commit "13341e6e0855c6b358ffcea6dad216e1009e1287"))) (file-name (git-file-name name version)) (sha256 (base32 "0c5p2dl8jb12ci9f427jzrmmm9cgvc1k4fxsn2ggkfsin6r1r82i")))) (build-system cmake-build-system) (arguments `(#:phases (modify-phases %standard-phases (replace 'check (lambda* (#:key tests? #:allow-other-keys) (when tests? (invoke "./bin/bioparser_test"))))))) (inputs (list biosoup)) (propagated-inputs (list zlib)) (native-inputs (list googletest)) (home-page "https://github.com/rvaser/bioparser") (synopsis "C++ library for parsing several formats in bioinformatics") (description "Bioparser is a C++ header only parsing library for several bioinformatics formats (FASTA/Q, MHAP/PAF/SAM), with support for zlib compressed files.") (license license:expat))) (define-public circtools (package (name "circtools") (version "1.0.0") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/Kevinzjy/circtools") ;; Corresponds to tag v1.0.0 (commit "79380de59013601021ca3b1352d6f64d2fb89646") (recursive? #t))) (file-name (git-file-name name version)) (sha256 (base32 "0wg1s927g32k25j967kfr8l30nmr4c0p4zvy5igvy7cs6chd60lh")))) (build-system cargo-build-system) (arguments `(#:phases (modify-phases %standard-phases (add-after 'unpack 'make-writable (lambda _ (for-each make-file-writable (find-files ".")))) (add-after 'unpack 'prepare-spoa-dependencies (lambda* (#:key inputs #:allow-other-keys) (substitute* "vendor/spoa/CMakeLists.txt" (("find_package\$bioparser 3.0.13 QUIET\$") "find_package(bioparser 3.0.13 CONFIG)") (("find_package\$biosoup 0.10.0 QUIET\$") "find_package(biosoup 0.10.0 CONFIG)") (("GTest_FOUND") "TRUE"))))) #:cargo-inputs (("rust-anyhow" ,rust-anyhow-1) ("rust-bio" ,rust-bio-0.33) ("rust-chrono" ,rust-chrono-0.4) ("rust-docopt" ,rust-docopt-1) ("rust-flate2" ,rust-flate2-1) ("rust-indicatif" ,rust-indicatif-0.15) ("rust-libc" ,rust-libc-0.2) ("rust-serde" ,rust-serde-1) ("rust-seq-io" ,rust-seq-io-0.3)))) (inputs (list bioparser biosoup)) (native-inputs (list cmake pkg-config googletest)) (home-page "https://github.com/Kevinzjy/circtools") (synopsis "Accelerating functions in CIRI toolkit") (description "This package provides accelerated functions for the CIRI toolkit. It also provides the @code{ccs} executable to scan for circular consensus sequences.") (license license:expat))) (define-public ciri-long (package (name "ciri-long") (version "1.0.2") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/bioinfo-biols/CIRI-long") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "10k88i1fcqchrrjv82rmylwvbwqfba0n51palhig9hsg71xs0dbi")) ;; Delete bundled binary (snippet '(delete-file "libs/ccs")))) (build-system python-build-system) (arguments `(#:phases (modify-phases %standard-phases (add-after 'unpack 'relax-requirements (lambda _ (substitute* "setup.py" (("'argparse[^']*',") "") ; only for python2 (("==") ">=")))) (add-before 'build 'build-libssw (lambda _ (with-directory-excursion "libs/striped_smith_waterman" (invoke "make" "libssw.so")))) (add-before 'build 'fix-reference-to-ccs (lambda* (#:key inputs #:allow-other-keys) (substitute* "CIRI_long/pipeline.py" (("'ccs -i") (string-append "'" (assoc-ref inputs "circtools") "/bin/ccs" " -i"))) ;; yuck! (substitute* "CIRI_long/main.py" (("os.chmod\\(lib_path.*") ""))))))) (inputs (list circtools python-biopython python-bwapy python-levenshtein python-mappy python-numpy python-pandas python-pysam python-pyspoa python-scikit-learn python-scipy)) (native-inputs (list python-cython python-nose python-setuptools)) (home-page "https://ciri-cookbook.readthedocs.io/") (synopsis "Circular RNA identification for Nanopore sequencing") (description "CIRI-long is a package for circular RNA identification using long-read sequencing data.") (license license:expat))) (define-public qtltools (package (name "qtltools") (version "1.3.1") (source (origin (method url-fetch/tarbomb) (uri (string-append "https://qtltools.github.io/qtltools/" "binaries/QTLtools_" version "_source.tar.gz")) (sha256 (base32 "13gdry5l43abn3464fmk8qzrxgxnxah2612r66p9dzhhl92j30cd")))) (build-system gnu-build-system) (arguments `(#:tests? #f ; no tests included #:make-flags ,#~(list (string-append "BOOST_INC=" #$(this-package-input "boost") "/include") (string-append "BOOST_LIB=" #$(this-package-input "boost") "/lib") (string-append "HTSLD_INC=" #$(this-package-input "htslib") "/include") (string-append "HTSLD_LIB=" #$(this-package-input "htslib") "/lib") (string-append "RMATH_INC=" #$(this-package-input "rmath-standalone") "/include") (string-append "RMATH_LIB=" #$(this-package-input "rmath-standalone") "/lib")) #:phases (modify-phases %standard-phases (add-after 'unpack 'fix-linkage (lambda _ (substitute* "qtltools/Makefile" (("libboost_iostreams.a") "libboost_iostreams.so") (("libboost_program_options.a") "libboost_program_options.so") (("-lblas") "-lopenblas")))) (add-before 'build 'chdir (lambda _ (chdir "qtltools"))) (replace 'configure (lambda _ (substitute* "qtltools/Makefile" (("LIB_FLAGS=-lz") "LIB_FLAGS=-lz -lcrypto -lssl") (("LIB_FILES=\\$\$RMATH_LIB\$/libRmath.a \ \\$\$HTSLD_LIB\$/libhts.a \ \\$\$BOOST_LIB\$/libboost_iostreams.a \ \\$\$BOOST_LIB\$/libboost_program_options.a") "LIB_FILES=$(RMATH_LIB)/libRmath.so \ $(HTSLD_LIB)/libhts.so \ $(BOOST_LIB)/libboost_iostreams.so \ $(BOOST_LIB)/libboost_program_options.so")))) (replace 'install (lambda* (#:key outputs #:allow-other-keys) (let ((bin (string-append (assoc-ref outputs "out") "/bin"))) (mkdir-p bin) (install-file "bin/QTLtools" bin))))))) (inputs (list curl gsl boost rmath-standalone htslib-1.3 openssl openblas zlib)) (home-page "https://qtltools.github.io/qtltools/") (synopsis "Tool set for molecular QTL discovery and analysis") (description "QTLtools is a tool set for molecular QTL discovery and analysis. It allows going from the raw genetic sequence data to collection of molecular @dfn{Quantitative Trait Loci} (QTLs) in few easy-to-perform steps.") (license license:gpl3+))) (define-public bpp-core (package (name "bpp-core") (version "2.4.1") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/BioPP/bpp-core") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "0ma2cl677l7s0n5sffh66cy9lxp5wycm50f121g8rx85p95vkgwv")))) (build-system cmake-build-system) ;; XXX: does not build with later GCC: ;; error: ‘numeric_limits’ was not declared in this scope (native-inputs (list gcc-10)) (home-page "https://pbil.univ-lyon1.fr/bpp-doc/bpp-core/html/index.html") (synopsis "C++ libraries for Bioinformatics") (description "Bio++ is a set of C++ libraries for Bioinformatics, including sequence analysis, phylogenetics, molecular evolution and population genetics. It is Object Oriented and is designed to be both easy to use and computer efficient. Bio++ intends to help programmers to write computer expensive programs, by providing them a set of re-usable tools.") (license license:cecill-c))) (define-public bpp-phyl (package (name "bpp-phyl") (version "2.4.1") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/BioPP/bpp-phyl") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "192zks6wyk903n06c2lbsscdhkjnfwms8p7jblsmk3lvjhdipb20")))) (build-system cmake-build-system) (inputs (list bpp-core bpp-seq)) (home-page "https://pbil.univ-lyon1.fr/bpp-doc/bpp-phyl/html/") (synopsis "Bio++ phylogenetic library") (description "Bio++ is a set of C++ libraries for Bioinformatics, including sequence analysis, phylogenetics, molecular evolution and population genetics. This library provides phylogenetics-related modules.") (license license:cecill-c))) (define-public bpp-phyl-omics (package (name "bpp-phyl-omics") (version "2.4.1") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/BioPP/bpp-phyl-omics") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "172psb8njkjwg3cd6gdy5w0mq8f0817v635yw4bk7146aggjzl1h")))) (build-system cmake-build-system) (arguments (list #:tests? #f)) ; No test provided. (inputs (list bpp-core bpp-phyl bpp-seq bpp-seq-omics)) (home-page "https://github.com/BioPP/bpp-phyl-omics") (synopsis "Bio++ phylogenetic library genomics components") (description "This library contains the genomics components of the Bio++ phylogenetics library. It is part of the Bio++ project.") (license license:cecill))) (define-public bpp-popgen (package (name "bpp-popgen") (version "2.4.1") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/BioPP/bpp-popgen") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "0bz0fhrq3dri6a0hvfc3zlvrns8mrzzlnicw5pyfa812gc1qwfvh")))) (build-system cmake-build-system) (arguments (list #:tests? #f)) ; There are no tests. (inputs (list bpp-core bpp-seq)) (home-page "https://pbil.univ-lyon1.fr/bpp-doc/bpp-popgen/html/") (synopsis "Bio++ population genetics library") (description "Bio++ is a set of C++ libraries for Bioinformatics, including sequence analysis, phylogenetics, molecular evolution and population genetics. This library provides population genetics-related modules.") (license license:cecill-c))) (define-public bpp-seq (package (name "bpp-seq") (version "2.4.1") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/BioPP/bpp-seq") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "1mc09g8jswzsa4wgrfv59jxn15ys3q8s0227p1j838wkphlwn2qk")))) (build-system cmake-build-system) (inputs (list bpp-core)) (home-page "https://pbil.univ-lyon1.fr/bpp-doc/bpp-seq/html/") (synopsis "Bio++ sequence library") (description "Bio++ is a set of C++ libraries for Bioinformatics, including sequence analysis, phylogenetics, molecular evolution and population genetics. This library provides sequence-related modules.") (license license:cecill-c))) (define-public bpp-seq-omics (package (name "bpp-seq-omics") (version "2.4.1") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/BioPP/bpp-seq-omics") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "1sc2xdfnfp5a6qihplp49rgrqmj89898avfy9bqaq1g2fajppgjj")))) (build-system cmake-build-system) (inputs (list bpp-core bpp-seq)) (home-page "https://github.com/BioPP/bpp-seq-omics") (synopsis "Bio++ sequence library genomics components") (description "This library contains the genomics components of the Bio++ sequence library. It is part of the Bio++ project.") (license license:cecill))) (define-public bppsuite (package (name "bppsuite") (version "2.4.1") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/BioPP/bppsuite") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "1wdwcgczqbc3m116vakvi0129wm3acln3cfc7ivqnalwvi6lrpds")))) (build-system cmake-build-system) (arguments (list #:tests? #f)) ; There are no tests. (native-inputs (list groff man-db texinfo)) (inputs (list bpp-core bpp-seq bpp-phyl bpp-popgen)) (home-page "https://github.com/BioPP") (synopsis "Bioinformatics tools written with the Bio++ libraries") (description "Bio++ is a set of C++ libraries for Bioinformatics, including sequence analysis, phylogenetics, molecular evolution and population genetics. This package provides command line tools using the Bio++ library.") (license license:cecill-c))) (define-public blast+ (package (name "blast+") (version "2.14.0") (source (origin (method url-fetch) (uri (string-append "https://ftp.ncbi.nlm.nih.gov/blast/executables/blast+/" version "/ncbi-blast-" version "+-src.tar.gz")) (sha256 (base32 "003mn7m4y306k7visv3in3ikfgm8m41z0jq9lyvz10iv1hdpyixz")) (modules '((guix build utils))) (snippet '(begin ;; Remove bundled bzip2, zlib and pcre. (delete-file-recursively "c++/src/util/compress/bzip2") (delete-file-recursively "c++/src/util/compress/zlib") (delete-file-recursively "c++/src/util/regexp") (substitute* "c++/src/util/compress/Makefile.in" (("bzip2 zlib api") "api")) ;; Remove useless msbuild directory (delete-file-recursively "c++/src/build-system/project_tree_builder/msbuild") ;; Build reproducibly. ;; Do not record the kernel version (substitute* "c++/src/build-system/configure" (("kver=.*") "kver=\"\"")) ;; Do not generate random numbers. (substitute* "c++/scripts/common/impl/define_random_macros.sh" (("#define NCBI_RANDOM_VALUE_MAX 0xffffffffu" m) (string-append m " #define NCBI_RANDOM_VALUE_0 2845495105u #define NCBI_RANDOM_VALUE_1 2158634051u #define NCBI_RANDOM_VALUE_2 4072202242u #define NCBI_RANDOM_VALUE_3 902228395u #define NCBI_RANDOM_VALUE_4 1353323915u #define NCBI_RANDOM_VALUE_5 574823513u #define NCBI_RANDOM_VALUE_6 4119501261u #define NCBI_RANDOM_VALUE_7 2477640938u #define NCBI_RANDOM_VALUE_8 2776595395u #define NCBI_RANDOM_VALUE_9 270550684u ")) (("cksum") "cksum >/dev/null")))))) (build-system gnu-build-system) (arguments (list ;; There are two(!) tests for this massive library, and both fail with ;; "unparsable timing stats". ;; ERR [127] -- [serial/datatool] datatool.sh (unparsable timing stats) ;; ERR [127] -- [serial/datatool] datatool_xml.sh (unparsable timing stats) #:tests? #f #:out-of-source? #t #:parallel-build? #f ;not supported #:phases #~(modify-phases %standard-phases (add-before 'configure 'set-HOME ;; $HOME needs to be set at some point during the configure phase (lambda _ (setenv "HOME" "/tmp"))) (add-after 'unpack 'enter-dir (lambda _ (chdir "c++"))) (add-after 'enter-dir 'fix-build-system (lambda _ (define (which* cmd) (cond ((string=? cmd "date") ;; make call to "date" deterministic "date -d @0") ((which cmd) => identity) (else (format (current-error-port) "WARNING: Unable to find absolute path for ~s~%" cmd) #false))) ;; Rewrite hardcoded paths to various tools (substitute* (append '("src/build-system/configure.ac" "src/build-system/configure" "src/build-system/helpers/run_with_lock.c" "scripts/common/impl/if_diff.sh" "scripts/common/impl/run_with_lock.sh" "src/build-system/Makefile.configurables.real" "src/build-system/Makefile.in.top" "src/build-system/Makefile.meta.gmake=no" "src/build-system/Makefile.meta.in" "src/build-system/Makefile.meta_l" "src/build-system/Makefile.meta_p" "src/build-system/Makefile.meta_r" "src/build-system/Makefile.mk.in" "src/build-system/Makefile.requirements" "src/build-system/Makefile.rules_with_autodep.in") (find-files "scripts/common/check" "\\.sh$")) (("(/usr/bin/|/bin/)([a-z][-_.a-z]*(\\+\\+)?)" all dir cmd) (or (which* cmd) all))) (substitute* (find-files "src/build-system" "^config.*") (("LN_S=/bin/\\$LN_S") (string-append "LN_S=" (which "ln"))) (("^PATH=.*") "")) ;; rewrite "/var/tmp" in check script (substitute* "scripts/common/check/check_make_unix.sh" (("/var/tmp") "/tmp")) ;; do not reset PATH (substitute* (find-files "scripts/common/impl/" "\\.sh$") (("^ *PATH=.*") "") (("action=/bin/") "action=") (("export PATH") ":")))) (replace 'configure (lambda _ (let ((lib (string-append #$output:lib "/lib")) (include (string-append #$output:include "/include/ncbi-tools++"))) ;; The 'configure' script doesn't recognize things like ;; '--enable-fast-install'. (invoke "./configure.orig" (string-append "--with-build-root=" (getcwd) "/build") (string-append "--prefix=" #$output) (string-append "--libdir=" lib) (string-append "--includedir=" include) (string-append "--with-bz2=" #$(this-package-input "bzip2")) (string-append "--with-z=" #$(this-package-input "zlib")) (string-append "--with-pcre=" #$(this-package-input "pcre")) ;; Each library is built twice by default, once ;; with "-static" in its name, and again ;; without. "--without-static" "--with-dll"))))))) (outputs '("out" ; 21 MB "lib" ; 226 MB "include")) ; 33 MB (inputs (list bzip2 lmdb zlib pcre perl python-wrapper)) (native-inputs (list cpio)) (home-page "https://blast.ncbi.nlm.nih.gov") (synopsis "Basic local alignment search tool") (description "BLAST is a popular method of performing a DNA or protein sequence similarity search, using heuristics to produce results quickly. It also calculates an “expect value” that estimates how many matches would have occurred at a given score by chance, which can aid a user in judging how much confidence to have in an alignment.") ;; Most of the sources are in the public domain, with the following ;; exceptions: ;; * Expat: ;; * ./c++/include/util/bitset/ ;; * ./c++/src/html/ncbi_menu*.js ;; * Boost license: ;; * ./c++/include/util/impl/floating_point_comparison.hpp ;; * LGPL 2+: ;; * ./c++/include/dbapi/driver/odbc/unix_odbc/ ;; * ASL 2.0: ;; * ./c++/src/corelib/teamcity_* (license (list license:public-domain license:expat license:boost1.0 license:lgpl2.0+ license:asl2.0)))) (define-public bless (package (name "bless") (version "1p02") (source (origin (method url-fetch) (uri (string-append "mirror://sourceforge/bless-ec/bless.v" version ".tgz")) (sha256 (base32 "0rm0gw2s18dqwzzpl3c2x1z05ni2v0xz5dmfk3d33j6g4cgrlrdd")) (modules '((guix build utils))) (snippet `(begin ;; Remove bundled boost, pigz, zlib, and .git directory ;; FIXME: also remove bundled sources for murmurhash3 and ;; kmc once packaged. (delete-file-recursively "boost") (delete-file-recursively "pigz") (delete-file-recursively "google-sparsehash") (delete-file-recursively "zlib") (delete-file-recursively ".git"))))) (build-system gnu-build-system) (arguments `(#:tests? #f ;no "check" target #:make-flags ,#~(list (string-append "ZLIB=" #$(this-package-input "zlib") "/lib/libz.so") (string-append "LDFLAGS=" (string-join '("-lboost_filesystem" "-lboost_system" "-lboost_iostreams" "-lz" "-fopenmp")))) #:phases (modify-phases %standard-phases (add-after 'unpack 'do-not-build-bundled-pigz (lambda* (#:key inputs outputs #:allow-other-keys) (substitute* "Makefile" (("cd pigz/pigz-2.3.3; make") "")))) (add-after 'unpack 'patch-paths-to-executables (lambda* (#:key inputs outputs #:allow-other-keys) (substitute* "parse_args.cpp" (("kmc_binary = .*") (string-append "kmc_binary = \"" (assoc-ref outputs "out") "/bin/kmc\";")) (("pigz_binary = .*") (string-append "pigz_binary = \"" (assoc-ref inputs "pigz") "/bin/pigz\";"))))) (replace 'install (lambda* (#:key outputs #:allow-other-keys) (let ((bin (string-append (assoc-ref outputs "out") "/bin/"))) (for-each (lambda (file) (install-file file bin)) '("bless" "kmc/bin/kmc"))))) (delete 'configure)))) (native-inputs (list perl)) (inputs (list openmpi boost sparsehash pigz zlib)) (supported-systems '("x86_64-linux")) (home-page "https://sourceforge.net/p/bless-ec/wiki/Home/") (synopsis "Bloom-filter-based error correction tool for NGS reads") (description "@dfn{Bloom-filter-based error correction solution for high-throughput sequencing reads} (BLESS) uses a single minimum-sized bloom filter is a correction tool for genomic reads produced by @dfn{Next-generation sequencing} (NGS). BLESS produces accurate correction results with much less memory compared with previous solutions and is also able to tolerate a higher false-positive rate. BLESS can extend reads like DNA assemblers to correct errors at the end of reads.") (license license:gpl3+))) (define-public bowtie (package (name "bowtie") (version "2.3.4.3") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/BenLangmead/bowtie2") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "1zl3cf327y2p7p03cavymbh7b00djc7lncfaqih33n96iy9q8ibp")) (modules '((guix build utils))) (snippet '(begin (substitute* "Makefile" ;; replace BUILD_HOST and BUILD_TIME for deterministic build (("-DBUILD_HOST=.*") "-DBUILD_HOST=\"\\\"guix\\\"\"") (("-DBUILD_TIME=.*") "-DBUILD_TIME=\"\\\"0\\\"\"")))))) (build-system gnu-build-system) (arguments `(#:make-flags ,#~(list "allall" "WITH_TBB=1" (string-append "prefix=" #$output)) #:phases (modify-phases %standard-phases (replace 'configure (lambda _ ;; This "extended character" is not considered valid. (substitute* "processor_support.h" (("“") "\"") (("”") "\"")))) (replace 'check (lambda _ (invoke "perl" "scripts/test/simple_tests.pl" "--bowtie2=./bowtie2" "--bowtie2-build=./bowtie2-build")))))) (inputs `(("tbb" ,tbb-2020) ("zlib" ,zlib) ("python" ,python-wrapper))) (native-inputs (list perl perl-clone perl-test-deep perl-test-simple)) (home-page "https://bowtie-bio.sourceforge.net/bowtie2/index.shtml") (synopsis "Fast and sensitive nucleotide sequence read aligner") (description "Bowtie 2 is a fast and memory-efficient tool for aligning sequencing reads to long reference sequences. It is particularly good at aligning reads of about 50 up to 100s or 1,000s of characters, and particularly good at aligning to relatively long (e.g. mammalian) genomes. Bowtie 2 indexes the genome with an FM Index to keep its memory footprint small: for the human genome, its memory footprint is typically around 3.2 GB. Bowtie 2 supports gapped, local, and paired-end alignment modes.") (supported-systems '("x86_64-linux")) (license license:gpl3+))) (define-public bowtie1 (package (name "bowtie1") (version "1.3.1") (source (origin (method url-fetch) (uri (string-append "mirror://sourceforge/bowtie-bio/bowtie/" version "/bowtie-" version "-src.zip")) (sha256 (base32 "0q87nhgj9wrnbazcpvqp4594hmyh1isi3s9b2wlghvl4afm1fdg2")) (modules '((guix build utils))) (snippet '(substitute* "Makefile" ;; replace BUILD_HOST and BUILD_TIME for deterministic build (("-DBUILD_HOST=.*") "-DBUILD_HOST=\"\\\"guix\\\"\"") (("-DBUILD_TIME=.*") "-DBUILD_TIME=\"\\\"0\\\"\""))))) (build-system gnu-build-system) (arguments `(#:tests? #f ; Tests need various perl modules #:test-target "simple-test" #:make-flags ,#~(append #$(if (not (target-x86?)) #~'("POPCNT_CAPABILITY=0") #~'()) (list (string-append "CC=" #$(cc-for-target)) (string-append "CXX=" #$(cxx-for-target)) "all" (string-append "prefix=" #$output))) #:phases (modify-phases %standard-phases (delete 'configure)))) (inputs (list python-wrapper tbb zlib)) (supported-systems %64bit-supported-systems) (home-page "https://bowtie-bio.sourceforge.net/index.shtml") (synopsis "Fast aligner for short nucleotide sequence reads") (description "Bowtie is a fast, memory-efficient short read aligner. It aligns short DNA sequences (reads) to the human genome at a rate of over 25 million 35-bp reads per hour. Bowtie indexes the genome with a Burrows-Wheeler index to keep its memory footprint small: typically about 2.2 GB for the human genome (2.9 GB for paired-end).") (license license:artistic2.0))) (define-public tophat (package (name "tophat") (version "2.1.1") (source (origin (method url-fetch) (uri (string-append "http://ccb.jhu.edu/software/tophat/downloads/tophat-" version ".tar.gz")) (sha256 (base32 "19add02kv2xhd6ihd779dr7x35ggym3jqr0m5c4315i1yfb0p11p")) (modules '((guix build utils))) (snippet '(begin ;; Remove bundled SeqAn and samtools (delete-file-recursively "src/SeqAn-1.4.2") (delete-file-recursively "src/samtools-0.1.18"))))) (build-system gnu-build-system) (arguments '(#:parallel-build? #f ; not supported #:phases (modify-phases %standard-phases (add-after 'set-paths 'hide-default-gcc (lambda* (#:key inputs #:allow-other-keys) (let ((gcc (assoc-ref inputs "gcc"))) ;; Remove the default GCC from CPLUS_INCLUDE_PATH to prevent ;; conflicts with the GCC 5 input. (setenv "CPLUS_INCLUDE_PATH" (string-join (delete (string-append gcc "/include/c++") (string-split (getenv "CPLUS_INCLUDE_PATH") #\:)) ":"))))) (add-after 'unpack 'use-system-samtools (lambda* (#:key inputs #:allow-other-keys) (substitute* "src/Makefile.in" (("(noinst_LIBRARIES = )\\$\$SAMLIB\$" _ prefix) prefix) (("\\$\$SAMPROG\$: \\$\$SAMLIB\$") "") (("SAMPROG = samtools_0\\.1\\.18") "") (("\\$\$samtools_0_1_18_SOURCES\$") "") (("am__EXEEXT_1 = samtools_0\\.1\\.18\\$\$EXEEXT\$") "")) (substitute* '("src/common.cpp" "src/tophat.py") (("samtools_0.1.18") (which "samtools"))) (substitute* '("src/common.h" "src/bam2fastx.cpp") (("#include \"bam.h\"") "#include <samtools/bam.h>") (("#include \"sam.h\"") "#include <samtools/sam.h>")) (substitute* '("src/bwt_map.h" "src/map2gtf.h" "src/align_status.h") (("#include <bam.h>") "#include <samtools/bam.h>") (("#include <sam.h>") "#include <samtools/sam.h>"))))))) (native-inputs `(("gcc@5" ,gcc-5))) ;; doesn't build with later versions (inputs `(("boost" ,boost) ("bowtie" ,bowtie) ("ncurses" ,ncurses) ("perl" ,perl) ("python" ,python-2) ("samtools" ,samtools-0.1) ("seqan" ,seqan-1) ("zlib" ,zlib))) (home-page "https://ccb.jhu.edu/software/tophat/index.shtml") (synopsis "Spliced read mapper for RNA-Seq data") (description "TopHat is a fast splice junction mapper for nucleotide sequence reads produced by the RNA-Seq method. It aligns RNA-Seq reads to mammalian-sized genomes using the ultra high-throughput short read aligner Bowtie, and then analyzes the mapping results to identify splice junctions between exons.") ;; TopHat is released under the Boost Software License, Version 1.0 ;; See https://github.com/infphilo/tophat/issues/11#issuecomment-121589893 (license license:boost1.0))) (define-public bwa (package (name "bwa") (version "0.7.18") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/lh3/bwa") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "1vf3iwkzxqkzhcfz2q3qyvcv3jrvbb012qy21pfgjl8lv20ywfr1")))) (build-system gnu-build-system) (arguments (list #:tests? #f ;no "check" target #:make-flags #~(list "CFLAGS=-fcommon" (string-append "CC=" #$(cc-for-target))) #:phases #~(modify-phases %standard-phases (replace 'install (lambda* (#:key outputs #:allow-other-keys) (let* ((out (assoc-ref outputs "out")) (bin (string-append out "/bin")) (lib (string-append out "/lib")) (doc (string-append out "/share/doc/bwa")) (man (string-append out "/share/man/man1"))) (install-file "bwa" bin) (install-file "libbwa.a" lib) (install-file "README.md" doc) (install-file "bwa.1" man)))) ;; no "configure" script (delete 'configure)))) (inputs (list zlib)) (supported-systems '("x86_64-linux" "aarch64-linux")) (home-page "https://bio-bwa.sourceforge.net/") (synopsis "Burrows-Wheeler sequence aligner") (description "BWA is a software package for mapping low-divergent sequences against a large reference genome, such as the human genome. It consists of three algorithms: BWA-backtrack, BWA-SW and BWA-MEM. The first algorithm is designed for Illumina sequence reads up to 100bp, while the rest two for longer sequences ranged from 70bp to 1Mbp. BWA-MEM and BWA-SW share similar features such as long-read support and split alignment, but BWA-MEM, which is the latest, is generally recommended for high-quality queries as it is faster and more accurate. BWA-MEM also has better performance than BWA-backtrack for 70-100bp Illumina reads.") (license license:gpl3+))) (define-public bwa-pssm (package (inherit bwa) (name "bwa-pssm") (version "0.5.11") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/pkerpedjiev/bwa-pssm") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "076c4q0cdqz8jgylb067y9zmvxglppnzi3qiscn0xiypgc6lgb5r")))) (build-system gnu-build-system) (arguments (substitute-keyword-arguments (package-arguments bwa) ((#:phases phases #~%standard-phases) #~(modify-phases #$phases (add-after 'unpack 'patch-C-error (lambda _ (substitute* "pssm.c" (("inline int map") "int map")))))))) (inputs (list gdsl zlib perl)) ;; https://bwa-pssm.binf.ku.dk is down, and all Web Archived copies are ;; blank (they actually have "display:none" for some nefarious reason). (home-page "https://github.com/pkerpedjiev/bwa-pssm") (synopsis "Burrows-Wheeler transform-based probabilistic short read mapper") (description "BWA-PSSM is a probabilistic short genomic sequence read aligner based on the use of @dfn{position specific scoring matrices} (PSSM). Like many of the existing aligners it is fast and sensitive. Unlike most other aligners, however, it is also adaptible in the sense that one can direct the alignment based on known biases within the data set. It is coded as a modification of the original BWA alignment program and shares the genome index structure as well as many of the command line options.") (license license:gpl3+))) (define-public bwa-meth (package (name "bwa-meth") (version "0.2.3") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/brentp/bwa-meth") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "0c695lkrr0996zwkibl7324wg2vxmn6522sz30xv4a9gaf0lnbh3")))) (build-system python-build-system) (arguments `(#:phases (modify-phases %standard-phases (add-after 'unpack 'keep-references-to-bwa (lambda* (#:key inputs #:allow-other-keys) (substitute* "bwameth.py" (("bwa (mem|index)" _ command) (string-append (which "bwa") " " command)) ;; There's an ill-advised check for "samtools" on PATH. (("^checkX.*") ""))))))) (inputs (list bwa)) (native-inputs (list python-toolshed)) (home-page "https://github.com/brentp/bwa-meth") (synopsis "Fast and accurante alignment of BS-Seq reads") (description "BWA-Meth works for single-end reads and for paired-end reads from the directional protocol (most common). It uses the method employed by methylcoder and Bismark of in silico conversion of all C's to T's in both reference and reads. It recovers the original read (needed to tabulate methylation) by attaching it as a comment which BWA appends as a tag to the read. It performs favorably to existing aligners gauged by number of on and off-target reads for a capture method that targets CpG-rich region.") (license license:expat))) (define-public python-bx-python (package (name "python-bx-python") (version "0.9.0") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/bxlab/bx-python") (commit "4f4a48d3f227ae390c1b22072867ba86e347bdef"))) (file-name (git-file-name name version)) (sha256 (base32 "1c914rw8phiw7zwzngz9i9hdciz5lq53drwdbpl2bd2sf5bj2biy")))) (build-system pyproject-build-system) (arguments (list #:phases '(modify-phases %standard-phases (add-before 'check 'build-extensions (lambda _ ;; Cython extensions have to be built before running the tests. (invoke "python" "setup.py" "build_ext" "--inplace"))) ;; Unrecognized argument. (add-after 'unpack 'disable-cython-doctests (lambda _ (substitute* "pytest.ini" (("--doctest-cython") ""))))))) (propagated-inputs (list python-numpy)) (inputs (list zlib)) (native-inputs (list python-cython python-lzo python-pytest)) (home-page "https://github.com/bxlab/bx-python") (synopsis "Tools for manipulating biological data") (description "bx-python provides tools for manipulating biological data, particularly multiple sequence alignments.") (license license:expat))) (define-public python-mofax ;; This is a recent commit from the "dev" branch, which is much more recent ;; than the latest commit from the "master" branch. (let ((commit "4d96f8f0a5d5251847353656f523684d66c3c47a") (revision "0")) (package (name "python-mofax") (version (git-version "0.4.0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/bioFAM/mofax") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "1lwrw0qyvvnyiqz1l20dhcf7dxidb80cqgvk78czvdgba87yxzqx")) (modules '((guix build utils))) ;; Prevent the pyproject-build-system from guessing that flit ;; should be used as a builder. (snippet '(substitute* "pyproject.toml" (("^#.*") ""))))) (build-system pyproject-build-system) (arguments (list ;; This test is failing due to a bug. The bug has been reported to the ;; developers. See https://github.com/bioFAM/mofax/issues/12 for more ;; info. #:test-flags '(list "-k" "not test_get_methods"))) (propagated-inputs (list python-h5py python-matplotlib python-pandas python-poetry-core python-scipy python-seaborn)) (native-inputs (list python-numpy python-pytest)) (home-page "https://github.com/bioFAM/mofax") (synopsis "Motif activity finder for transcription factor motif analysis") (description "MoFax is a Python package for transcription factor motif analysis. It provides convenience functions to load and visualize factor models trained with MOFA+ in Python.") (license license:expat)))) (define-public python-mudata (package (name "python-mudata") (version "0.2.3") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/scverse/mudata") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "02h0k1q57589r0hdv8nwg1vk7g2ljvn5g66c47fy5gdilbm3gjws")))) (build-system pyproject-build-system) (propagated-inputs (list python-anndata python-h5py python-pandas)) (native-inputs (list python-flit-core python-numpy python-pytest python-zarr)) (home-page "https://github.com/scverse/mudata") (synopsis "Python package for multi-omics data analysis") (description "Mudata is a Python package for multi-omics data analysis. It is designed to provide functionality to load, process, and store multimodal omics data.") (license license:bsd-3))) (define-public python-mofapy2 (package (name "python-mofapy2") (version "0.7.1") (source (origin ;; The tarball from PyPi doesn't include tests. (method git-fetch) (uri (git-reference (url "https://github.com/bioFAM/mofapy2") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "0ahhnqk6gjrhyq286mrd5n7mxcv8l6040ffsawbjx9maqx8wbam0")))) (build-system pyproject-build-system) (arguments (list #:test-flags ;; cupy is an optional dependency, which ;; itself has nonfree dependencies (CUDA) '(list "--ignore=mofapy2/notebooks/test_cupy.py"))) (propagated-inputs (list python-anndata python-h5py python-numpy python-pandas python-scikit-learn python-scipy)) (native-inputs (list python-poetry-core python-pytest)) (home-page "https://biofam.github.io/MOFA2/") (synopsis "Multi-omics factor analysis") (description "MOFA is a factor analysis model that provides a general framework for the integration of multi-omic data sets in an unsupervised fashion. Intuitively, MOFA can be viewed as a versatile and statistically rigorous generalization of principal component analysis to multi-omics data. Given several data matrices with measurements of multiple -omics data types on the same or on overlapping sets of samples, MOFA infers an interpretable low-dimensional representation in terms of a few latent factors. These learnt factors represent the driving sources of variation across data modalities, thus facilitating the identification of cellular states or disease subgroups.") (license license:lgpl3))) (define-public python-muon (package (name "python-muon") (version "0.1.6") (source (origin ;; The tarball from PyPi doesn't include tests. (method git-fetch) (uri (git-reference (url "https://github.com/scverse/muon") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "1kd3flgy41dc0sc71wfnirh8vk1psxgyjxkbx1zx9yskkh6anbgw")))) (build-system pyproject-build-system) (arguments (list #:test-flags ;; Even providing a random seed, scipy.sparse.rand produces inconsistent ;; results across scipy versions. '(list "-k" "not test_tfidf") #:phases '(modify-phases %standard-phases ;; Numba needs a writable dir to cache functions. (add-before 'build 'set-numba-cache-dir (lambda _ (setenv "NUMBA_CACHE_DIR" "/tmp")))))) (propagated-inputs (list python-anndata python-h5py python-matplotlib python-mofapy2 python-mudata python-numba python-numpy python-pandas python-protobuf python-pybedtools python-pysam python-scanpy python-scikit-learn python-seaborn python-tqdm python-umap-learn)) (native-inputs (list python-flit-core python-pytest python-pytest-flake8)) (home-page "https://github.com/scverse/muon") (synopsis "Multimodal omics analysis framework") (description "muon is a multimodal omics Python framework.") (license license:bsd-3))) (define-public python-pyega3 (deprecated-package "python-pyega3" python-ega-download-client)) (define-public python-pysam (package (name "python-pysam") (version "0.20.0") (source (origin (method git-fetch) ;; Test data is missing on PyPi. (uri (git-reference (url "https://github.com/pysam-developers/pysam") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "1dq6jwwm98lm30ijdgqc5xz5ppda4nj999y6qs78mhw8x0kij8gg")) (modules '((guix build utils))) (snippet '(begin ;; FIXME: Unbundle samtools and bcftools. (delete-file-recursively "htslib"))))) (build-system pyproject-build-system) (arguments `(#:phases (modify-phases %standard-phases (add-before 'build 'set-flags (lambda* (#:key inputs #:allow-other-keys) (setenv "HTSLIB_MODE" "external") (setenv "HTSLIB_LIBRARY_DIR" (string-append (assoc-ref inputs "htslib") "/lib")) (setenv "HTSLIB_INCLUDE_DIR" (string-append (assoc-ref inputs "htslib") "/include")) (setenv "LDFLAGS" "-lncurses") (setenv "CFLAGS" "-D_CURSES_LIB=1"))) (replace 'check (lambda* (#:key tests? #:allow-other-keys) (when tests? ;; Step out of source dir so python does not import from CWD. (with-directory-excursion "tests" (setenv "HOME" "/tmp") (invoke "make" "-C" "pysam_data") (invoke "make" "-C" "cbcf_data") ;; The FileHTTP test requires network access. (invoke "pytest" "-k" "not FileHTTP")))))))) (propagated-inputs (list htslib)) ; Included from installed header files. (inputs (list ncurses curl zlib)) (native-inputs (list python-cython python-pytest ;; Dependencies below are are for tests only. samtools bcftools)) (home-page "https://github.com/pysam-developers/pysam") (synopsis "Python bindings to the SAMtools C API") (description "Pysam is a Python module for reading and manipulating files in the SAM/BAM format. Pysam is a lightweight wrapper of the SAMtools C API. It also includes an interface for tabix.") (license license:expat))) (define-public python-twobitreader (package (name "python-twobitreader") (version "3.1.6") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/benjschiller/twobitreader") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "1qbxvv1h58cismbk1anpjrkpghsaiy64a11ir3lhy6qch6xf8n62")))) (build-system python-build-system) ;; Tests are not included (arguments '(#:tests? #f)) (native-inputs (list python-sphinx)) (home-page "https://github.com/benjschiller/twobitreader") (synopsis "Python library for reading .2bit files") (description "twobitreader is a Python library for reading .2bit files as used by the UCSC genome browser.") (license license:artistic2.0))) (define-public python-plastid (package (name "python-plastid") (version "0.6.1") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/joshuagryphon/plastid") (commit "d97f239d73b3a7c2eff46f71928b777431891f90"))) (file-name (git-file-name name version)) (sha256 (base32 "0iccpywlpf1ws46279z9rl0l29pil0rj0g2j5nvqq7jfbnq581cf")))) (build-system pyproject-build-system) (arguments (list #:test-flags '(list "plastid/test" ;; These four failures look like errors in the test wrapper ;; class. "-k" (string-append "not test_chrom_sizes" " and not test_no_crash_if_file_not_exist" " and not test_fiveprime_variable" " and not test_fiveprime_variable_from_file")) #:phases #~(modify-phases %standard-phases (add-after 'unpack 'unpack-test-data (lambda* (#:key inputs #:allow-other-keys) (invoke "tar" "-C" "plastid/test" "-xf" (assoc-ref inputs "test-data")) ;; This one requires bowtie-build (delete-file "plastid/test/functional/test_crossmap.py"))) (add-after 'unpack 'patch-for-python-3.10 (lambda _ ;; Some classes were moved from collections to collections.abc ;; in Python 3.10. (substitute* "plastid/readers/bigbed.pyx" ((", Iterable") "\nfrom collections.abc import Iterable")))) (add-before 'check 'build-extensions (lambda _ ;; Cython extensions have to be built before running the tests. (invoke "python3" "setup.py" "build_ext" "--inplace")))))) (propagated-inputs (list python-numpy python-scipy python-pandas python-pysam python-matplotlib python-biopython python-twobitreader python-termcolor)) (inputs (list openssl)) (native-inputs `(("python-cython" ,python-cython) ("python-pytest" ,python-pytest) ("test-data" ,(origin (method url-fetch) (uri "https://www.dropbox.com/s/np3wlfvp6gx8tb8/2022-05-04.plastid-test-data.tar.bz2?dl=1") (file-name "plastid-test-data-2022-05-04.tar.bz2") (sha256 (base32 "1szsji06m2r21flnvxg84jnj5zmlk6z10c9651v9ag71nxj9rbzn")))))) (home-page "https://github.com/joshuagryphon/plastid") (synopsis "Python library for genomic analysis") (description "plastid is a Python library for genomic analysis – in particular, high-throughput sequencing data – with an emphasis on simplicity.") (license license:bsd-3))) (define-public tetoolkit (package (name "tetoolkit") (version "2.2.1b") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/mhammell-laboratory/TEtranscripts") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "1m3xsydakhdan9gp9mfdz7llka5g6ak91d0mbl1cmmxq9qs6an4y")))) (build-system python-build-system) (arguments `(#:phases (modify-phases %standard-phases (add-after 'unpack 'adjust-requirements (lambda _ (substitute* "setup.py" ;; This defunct dependency isn't required for Python 3 (see: ;; https://github.com/mhammell-laboratory/TEtranscripts/issues/111). ((".*'argparse'.*") "")))) (add-after 'unpack 'patch-invocations (lambda* (#:key inputs #:allow-other-keys) (substitute* '("bin/TEtranscripts" "bin/TEcount") (("'sort ") (string-append "'" (search-input-file inputs "bin/sort") " ")) (("'rm -f ") (string-append "'" (search-input-file inputs "bin/rm") " -f ")) (("'Rscript'") (string-append "'" (search-input-file inputs "bin/Rscript") "'"))) (substitute* "TEToolkit/IO/ReadInputs.py" (("BamToBED") (search-input-file inputs "bin/bamToBed"))) (substitute* "TEToolkit/Normalization.py" (("\"Rscript\"") (string-append "\"" (search-input-file inputs "bin/Rscript") "\""))))) (add-after 'install 'wrap-program (lambda* (#:key outputs #:allow-other-keys) ;; Make sure the executables find R packages. (for-each (lambda (script) (wrap-program script `("R_LIBS_SITE" ":" = (,(getenv "R_LIBS_SITE"))))) (list (search-input-file outputs "bin/TEtranscripts") (search-input-file outputs "bin/TEcount")))))))) (inputs (list bash-minimal coreutils bedtools python-pysam r-minimal r-deseq2)) (home-page "https://github.com/mhammell-laboratory/TEtranscripts") (synopsis "Transposable elements in differential enrichment analysis") (description "This is package for including transposable elements in differential enrichment analysis of sequencing datasets. TEtranscripts and TEcount take RNA-seq (and similar data) and annotates reads to both genes and transposable elements. TEtranscripts then performs differential analysis using DESeq2. Note that TEtranscripts and TEcount rely on specially curated GTF files, which are not included due to their size.") (license license:gpl3+))) (define-public cd-hit (package (name "cd-hit") (version "4.8.1") (source (origin (method url-fetch) (uri (string-append "https://github.com/weizhongli/cdhit" "/releases/download/V" version "/cd-hit-v" version "-2019-0228.tar.gz")) (sha256 (base32 "1phmfhgcpyfd6kj7jwzw976613lcpv1wc2pzfdfaxla062x2s5r6")))) (build-system gnu-build-system) (arguments (list #:tests? #f ; there are no tests #:make-flags ;; Executables are copied directly to the PREFIX. #~(list (string-append "PREFIX=" #$output "/bin") ;; Support longer sequences (e.g. Pacbio sequences) "MAX_SEQ=60000000") #:phases '(modify-phases %standard-phases ;; No "configure" script (delete 'configure) ;; Remove sources of non-determinism (add-after 'unpack 'be-timeless (lambda _ (substitute* "cdhit-utility.c++" ((" \$built on \" __DATE__ \"\$") "")) (substitute* "cdhit-common.c++" (("__DATE__") "\"0\"") (("\", %s, \" __TIME__ \"\\\\n\", date") "")))) ;; The "install" target does not create the target directory. (add-before 'install 'create-target-dir (lambda* (#:key outputs #:allow-other-keys) (mkdir-p (string-append (assoc-ref outputs "out") "/bin"))))))) (inputs (list perl zlib)) (home-page "http://weizhongli-lab.org/cd-hit/") (synopsis "Cluster and compare protein or nucleotide sequences") (description "CD-HIT is a program for clustering and comparing protein or nucleotide sequences. CD-HIT is designed to be fast and handle extremely large databases.") ;; The manual says: "It can be copied under the GNU General Public License ;; version 2 (GPLv2)." (license license:gpl2))) (define-public cd-hit-auxtools (package (inherit cd-hit) (name "cd-hit-auxtools") (arguments (list #:tests? #f ; there are no tests #:phases #~(modify-phases %standard-phases (add-after 'unpack 'chdir (lambda _ (chdir "cd-hit-auxtools"))) ;; No "configure" script (delete 'configure) ;; There is no install target. (replace 'install (lambda _ (for-each (lambda (file) (install-file file (string-append #$output "/bin"))) '("cd-hit-dup" "cd-hit-lap" "read-linker"))))))) (inputs '()))) (define-public clipper (package (name "clipper") (version "2.0.1") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/YeoLab/clipper") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "0508rgnfjk5ar5d1mjbjyrnarv4kw9ksq0m3jw2bmgabmb5v6ikk")) (modules '((guix build utils))) (snippet '(begin ;; Delete pre-compiled files. (delete-file "clipper/src/peaks.so"))))) (build-system python-build-system) (arguments `(#:tests? #false #:phases (modify-phases %standard-phases (add-after 'unpack 'use-python3-for-cython (lambda _ (substitute* "setup.py" (("^setup") "\ peaks.cython_directives = {'language_level': '3'} readsToWiggle.cython_directives = {'language_level': '3'} setup")))) (add-after 'unpack 'disable-nondeterministic-test (lambda _ ;; This test fails/succeeds non-deterministically. (substitute* "clipper/test/test_call_peak.py" (("test_get_FDR_cutoff_mean") "_test_get_FDR_cutoff_mean")))) ;; This doesn't work because "usage" is executed, and that calls ;; exit(8). (replace 'check (lambda* (#:key tests? inputs outputs #:allow-other-keys) (when tests? (add-installed-pythonpath inputs outputs) (with-directory-excursion "clipper/test" (invoke "python" "-m" "unittest"))))) ;; This is not a library (delete 'sanity-check)))) (inputs (list htseq python-pybedtools python-cython python-scikit-learn python-matplotlib python-pandas python-pysam python-numpy python-scipy)) (native-inputs (list python-setuptools-git python-mock ; for tests python-nose ; for tests python-pytz)) ; for tests (home-page "https://github.com/YeoLab/clipper") (synopsis "CLIP peak enrichment recognition") (description "CLIPper is a tool to define peaks in CLIP-seq datasets.") (license license:gpl2))) (define-public codingquarry (package (name "codingquarry") (version "2.0") (source (origin (method url-fetch) (uri (string-append "mirror://sourceforge/codingquarry/CodingQuarry_v" version ".tar.gz")) (sha256 (base32 "0115hkjflsnfzn36xppwf9h9avfxlavr43djqmshkkzbgjzsz60i")))) (build-system gnu-build-system) (arguments (list #:tests? #f ;no "check" target #:phases #~(modify-phases %standard-phases (delete 'configure) (replace 'install (lambda _ (let ((bin (string-append #$output "/bin")) (doc (string-append #$output "/share/doc/codingquarry"))) (install-file "INSTRUCTIONS.pdf" doc) (copy-recursively "QuarryFiles" (string-append #$output "/share/codingquarry/QuarryFiles")) (install-file "CodingQuarry" bin) (install-file "CufflinksGTF_to_CodingQuarryGFF3.py" bin))))))) ;; TODO: This package also needs a Python 2 variant of biopython (inputs (list openmpi python-2)) ;Only Python 2 is supported (native-search-paths (list (search-path-specification (variable "QUARRY_PATH") (files '("share/codingquarry/QuarryFiles"))))) (home-page "https://sourceforge.net/projects/codingquarry/") (synopsis "Fungal gene predictor") (description "CodingQuarry is a highly accurate, self-training GHMM fungal gene predictor designed to work with assembled, aligned RNA-seq transcripts.") (license license:gpl3+))) (define-public clustal-omega (package (name "clustal-omega") (version "1.2.4") (source (origin (method url-fetch) (uri (string-append "http://www.clustal.org/omega/clustal-omega-" version ".tar.gz")) (sha256 (base32 "1vm30mzncwdv881vrcwg11vzvrsmwy4wg80j5i0lcfk6dlld50w6")))) (build-system gnu-build-system) (inputs (list argtable)) (home-page "http://www.clustal.org/omega/") (synopsis "Multiple sequence aligner for protein and DNA/RNA") (description "Clustal-Omega is a general purpose multiple sequence alignment (MSA) program for protein and DNA/RNA. It produces high quality MSAs and is capable of handling data-sets of hundreds of thousands of sequences in reasonable time.") (license license:gpl2+))) (define-public crossmap (package (name "crossmap") (version "0.6.1") (source (origin (method url-fetch) (uri (pypi-uri "CrossMap" version)) (sha256 (base32 "0hqminh5wn1p3x481jbyc7gmncp5xc196hpvki7k25vzbryhwcix")) (modules '((guix build utils))) (snippet '(begin ;; Delete compiled Python files. (for-each delete-file (find-files "." "\\.pyc$")) (delete-file-recursively ".eggs"))))) (build-system python-build-system) (inputs (list python-bx-python python-numpy python-pybigwig python-pysam zlib)) (native-inputs (list python-cython python-nose)) (home-page "https://crossmap.sourceforge.net/") (synopsis "Convert genome coordinates between assemblies") (description "CrossMap is a program for conversion of genome coordinates or annotation files between different genome assemblies. It supports most commonly used file formats including SAM/BAM, Wiggle/BigWig, BED, GFF/GTF, VCF.") (license license:gpl2+))) (define-public python-dnaio (package (name "python-dnaio") (version "0.10.0") (source (origin (method url-fetch) (uri (pypi-uri "dnaio" version)) (sha256 (base32 "064xc4j8plb4fpkm8mw55715mvpvi2sxsknpjx18c2zh904salfy")))) (build-system pyproject-build-system) (arguments (list #:tests? #false)) ;there are none (native-inputs (list python-cython python-pytest python-setuptools-scm)) (propagated-inputs (list python-xopen)) (home-page "https://github.com/marcelm/dnaio/") (synopsis "Read FASTA and FASTQ files efficiently") (description "dnaio is a Python library for fast parsing of FASTQ and also FASTA files. The code was previously part of the cutadapt tool.") (license license:expat))) (define-public python-deeptoolsintervals (package (name "python-deeptoolsintervals") (version "0.1.9") (source (origin (method url-fetch) (uri (pypi-uri "deeptoolsintervals" version)) (sha256 (base32 "1xnl80nblysj6dylj4683wgrfa425rkx4dp5k65hvwdns9pw753x")))) (build-system python-build-system) (inputs (list zlib)) (home-page "https://github.com/deeptools/deeptools_intervals") (synopsis "Create GTF-based interval trees with associated meta-data") (description "This package provides a Python module creating/accessing GTF-based interval trees with associated meta-data. It is primarily used by the @code{deeptools} package.") (license license:expat))) (define-public python-deeptools (package (name "python-deeptools") (version "3.5.5") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/deeptools/deepTools") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "0mgcs03amrd5157drbm6ikdg0m0szrn9xbflariz2zrrnqpsai6s")))) (build-system pyproject-build-system) (arguments (list #:phases #~(modify-phases %standard-phases (add-after 'unpack 'fix-test (lambda _ (substitute* "deeptools/test/test_tools.py" (("e_ver = _p") "e_ver = \".\" + _p + \"-real\"")) (substitute* "deeptools/multiBigwigSummary.py" (("version='multiBigwigSummary") "version='%(prog)s")) (substitute* "deeptools/plotCoverage.py" (("version='plotCoverage") "version='%(prog)s"))))))) (native-inputs (list python-mock python-pytest)) (propagated-inputs (list python-matplotlib python-numpy python-numpydoc python-py2bit python-pybigwig python-pysam python-scipy python-deeptoolsintervals python-plotly)) (home-page "https://pypi.org/project/deepTools/") (synopsis "Useful tools for exploring deep sequencing data") (description "This package addresses the challenge of handling large amounts of data that are now routinely generated from DNA sequencing centers. @code{deepTools} contains useful modules to process the mapped reads data for multiple quality checks, creating normalized coverage files in standard bedGraph and bigWig file formats, that allow comparison between different files. Finally, using such normalized and standardized files, deepTools can create many publication-ready visualizations to identify enrichments and for functional annotations of the genome.") ;; The file deeptools/cm.py is licensed under the BSD license. The ;; remainder of the code is licensed under the MIT license. (license (list license:bsd-3 license:expat)))) (define-public cutadapt (package (name "cutadapt") (version "4.0") (source (origin (method url-fetch) (uri (pypi-uri "cutadapt" version)) (sha256 (base32 "0xgsv88mrlw2b1radmd1104y7bg8hvv54ay7xfdpnjiw2jgkrha9")))) (build-system pyproject-build-system) (arguments (list #:test-flags '(list "-k" "not test_no_read_only_comment_fasta_input") #:phases #~(modify-phases %standard-phases (add-after 'unpack 'fix-test (lambda _ (let ((site (string-append #$output "/lib/python" #$(version-major+minor (package-version python)) "/site-packages"))) (substitute* "tests/test_command.py" (("env=\\{\"LC_CTYPE\": \"C\"\\},") (string-append "env={\"LC_CTYPE\": \"C\", \"GUIX_PYTHONPATH\": \"" (getenv "GUIX_PYTHONPATH") ":" site "\"},"))))))))) (inputs (list python-dnaio python-xopen)) (native-inputs (list python-cython python-pytest python-pytest-mock python-pytest-timeout python-setuptools-scm)) (home-page "https://cutadapt.readthedocs.io/en/stable/") (synopsis "Remove adapter sequences from nucleotide sequencing reads") (description "Cutadapt finds and removes adapter sequences, primers, poly-A tails and other types of unwanted sequence from high-throughput sequencing reads.") (license license:expat))) (define-public lammps (let ((commit "stable_2Aug2023_update2")) (package (name "lammps") (version (string-append "0." commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/lammps/lammps.git") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "11xagacgxgldkx34qdzyjrjvn8x3hpl0kgzhh9zh7skpq79pwycz")))) (build-system gnu-build-system) (arguments (list #:tests? #f ; no check target #:make-flags '(list "CC=mpicc" "mpi" "LMP_INC=-DLAMMPS_GZIP \ -DLAMMPS_JPEG -DLAMMPS_PNG -DLAMMPS_FFMPEG -DLAMMPS_MEMALIGN=64" "LIB=-gz -ljpeg -lpng -lavcodec") #:phases #~(modify-phases %standard-phases (add-after 'unpack 'chdir (lambda _ (chdir "src"))) (replace 'configure (lambda _ (substitute* "MAKE/Makefile.mpi" (("SHELL =.*") (string-append "SHELL=" (which "bash") "\n")) (("cc ") "mpicc ")) (substitute* "Makefile" (("SHELL =.*") (string-append "SHELL=" (which "bash") "\n"))))) (add-after 'configure 'configure-modules (lambda _ (invoke "make" "yes-molecule" "yes-misc" "yes-granular" (string-append "HDF5_PATH=" #$(this-package-input "hdf5"))))) (replace 'install (lambda _ (let ((bin (string-append #$output "/bin"))) (mkdir-p bin) (install-file "lmp_mpi" bin))))))) (inputs (list ffmpeg gfortran gzip hdf5 libjpeg-turbo libpng openmpi python-wrapper)) (native-inputs (list bc)) (home-page "https://www.lammps.org/") (synopsis "Classical molecular dynamics simulator") (description "LAMMPS is a classical molecular dynamics simulator designed to run efficiently on parallel computers. LAMMPS has potentials for solid-state materials (metals, semiconductors), soft matter (biomolecules, polymers), and coarse-grained or mesoscopic systems. It can be used to model atoms or, more generically, as a parallel particle simulator at the atomic, meso, or continuum scale.") (license license:gpl2+)))) (define-public lammps-serial (package (inherit lammps) (name "lammps-serial") (arguments (substitute-keyword-arguments (package-arguments lammps) ((#:make-flags flags) '(list "CC=gcc" "serial" "LMP_INC=-DLAMMPS_GZIP \ -DLAMMPS_JPEG -DLAMMPS_PNG -DLAMMPS_FFMPEG -DLAMMPS_MEMALIGN=64" "LIB=-gz -ljpeg -lpng -lavcodec")) ((#:phases phases) #~(modify-phases #$phases (replace 'configure (lambda _ (substitute* "MAKE/Makefile.serial" (("SHELL =.*") (string-append "SHELL=" (which "bash") "\n")) (("cc ") "gcc ")) (substitute* "Makefile" (("SHELL =.*") (string-append "SHELL=" (which "bash") "\n"))))) (replace 'install (lambda _ (let ((bin (string-append #$output "/bin"))) (mkdir-p bin) (install-file "lmp_serial" bin)))))))) (inputs (modify-inputs (package-inputs lammps) (delete "openmpi"))))) (define-public libbigwig (package (name "libbigwig") (version "0.4.4") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/dpryan79/libBigWig") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "09693dmf1scdac5pyq6qyn8b4mcipvnmc370k9a5z41z81m3dcsj")))) (build-system gnu-build-system) (arguments `(#:test-target "test" #:tests? #f ; tests require access to the web #:make-flags ,#~(list "CC=gcc" (string-append "prefix=" #$output)) #:phases (modify-phases %standard-phases (delete 'configure)))) (inputs (list zlib curl)) (native-inputs `(("doxygen" ,doxygen) ;; Need for tests ("python" ,python-2))) (home-page "https://github.com/dpryan79/libBigWig") (synopsis "C library for handling bigWig files") (description "This package provides a C library for parsing local and remote BigWig files.") (license license:expat))) (define-public lsgkm (package (name "lsgkm") (version "0.1.1") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/Dongwon-Lee/lsgkm.git") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "0b3m94kndvimdfjaf1q2yhmsn7lm5s9v81c5xgfjcp6ig7mh3sa5")))) (build-system gnu-build-system) (arguments (list #:make-flags '(list "-C" "src") #:tests? #false ;there are no executable tests #:phases #~(modify-phases %standard-phases (delete 'configure) (replace 'install (lambda _ (let ((bin (string-append #$output "/bin"))) (for-each (lambda (file) (install-file file bin)) '("src/gkmtrain" "src/gkmpredict")))))))) (home-page "https://github.com/Dongwon-Lee/lsgkm") (synopsis "Predict regulatory DNA elements in large-scale data") (description "gkm-SVM, a sequence-based method for predicting regulatory DNA elements, is a useful tool for studying gene regulatory mechanisms. LS-GKM is an effort to improve the method. It offers much better scalability and provides further advanced gapped k-mer based kernel functions. As a result, LS-GKM achieves considerably higher accuracy than the original gkm-SVM.") (license license:gpl3+))) (define-public python-fcsparser (package (name "python-fcsparser") (version "0.2.8") (source (origin (method url-fetch) (uri (pypi-uri "fcsparser" version)) (sha256 (base32 "1skk1k8phq9sj4ar0cnq8px89y3kcyh5zrbl6anz9wcdcyzkc16z")))) (build-system pyproject-build-system) (propagated-inputs (list python-numpy python-pandas)) (native-inputs (list python-poetry-core python-pytest)) (home-page "https://github.com/eyurtsev/fcsparser") (synopsis "Package for reading raw fcs files") (description "This package provides a Python package for reading raw fcs files") (license license:expat))) (define-public python-pybigwig (package (name "python-pybigwig") (version "0.3.22") (source (origin (method url-fetch) (uri (pypi-uri "pyBigWig" version)) (sha256 (base32 "0hr25lkp26mk0fp7irdjdrdsd5lann9kyv0xq9npyyxxakvjci2x")) (modules '((guix build utils))) (snippet ;; Delete bundled libBigWig sources '(delete-file-recursively "libBigWig")))) (build-system pyproject-build-system) (arguments '(#:tests? #false ;only one test exists and it needs internet access #:phases (modify-phases %standard-phases (add-after 'unpack 'link-with-libBigWig (lambda _ (substitute* "setup.py" (("libs=\\[") "libs=[\"BigWig\", "))))))) (propagated-inputs (list python-numpy)) (inputs (list libbigwig zlib curl)) (home-page "https://github.com/dpryan79/pyBigWig") (synopsis "Access bigWig files in Python using libBigWig") (description "This package provides Python bindings to the libBigWig library for accessing bigWig files.") (license license:expat))) (define-public python-pyfasta ;; The release on pypi does not contain the test data files. (let ((commit "c2f0611c5311f1b1466f2d56560447898b4a8b03") (revision "1")) (package (name "python-pyfasta") (version (git-version "0.5.2" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/brentp/pyfasta") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0a189id3fbv88gssyk6adbmz2ll1mqpmyw8vxmx3fi955gvaq9j7")))) (build-system pyproject-build-system) (arguments (list #:phases '(modify-phases %standard-phases (add-after 'unpack 'python3.10-compat (lambda _ (substitute* "pyfasta/__init__.py" (("from fasta import") "from pyfasta.fasta import") (("from records import") "from pyfasta.records import") (("from split_fasta import") "from pyfasta.split_fasta import") (("in f.iteritems") "in f.items")) (substitute* "pyfasta/fasta.py" (("from collections import Mapping") "from collections.abc import Mapping") (("from records import") "from pyfasta.records import")) (substitute* "pyfasta/records.py" (("cPickle") "pickle") (("\$int, long\$") "(int, int)") ;; XXX: it's not clear if this is really correct. (("buffer\$self\$") "memoryview(bytes(str(self), encoding='utf-8'))") (("sys.maxint") "sys.maxsize")) (substitute* "pyfasta/split_fasta.py" (("from cStringIO import") "from io import") (("in lens.iteritems") "in lens.items")) (substitute* "tests/test_all.py" (("f.keys\$\$\\) == \\['a-extra'") "list(f.keys())) == ['a-extra'") (("f.iterkeys\$\$") "iter(f.keys())") (("tests/data/" m) (string-append (getcwd) "/" m)))))))) (propagated-inputs (list python-numpy)) (native-inputs (list python-nose)) (home-page "https://github.com/brentp/pyfasta/") (synopsis "Pythonic access to fasta sequence files") (description "This library provides fast, memory-efficient, pythonic (and command-line) access to fasta sequence files. It stores a flattened version of a fasta sequence file without spaces or headers and uses either a @code{mmap} in numpy binary format or @code{fseek}/@code{fread} so the sequence data is never read into memory. It saves a pickle (@code{.gdx}) of the start and stop (for @code{fseek}/@code{mmap}) locations of each header in the fasta file for internal use. Note that this package has been deprecated in favor of @code{pyfaidx}.") (license license:expat)))) (define-public python-schema-salad (package (name "python-schema-salad") (version "8.5.20240102191335") (source (origin (method url-fetch) (uri (pypi-uri "schema-salad" version)) (sha256 (base32 "035202p696i3jylb8b3nm9qcxsqby15hhqn1dl4nrz73a17p0ckx")))) (build-system pyproject-build-system) (arguments (list #:phases #~(modify-phases %standard-phases (add-after 'unpack 'set-version (lambda _ ;; Set exact version. (substitute* "setup.py" (("use_scm_version=True") (string-append "version=\"" #$version "\""))))) (add-before 'check 'skip-failing-tests (lambda _ ;; Skip tests that require network access. (let ((skip-test (lambda (test-pattern) (string-append "@pytest.mark.skip(reason=" "\"test requires network access\")\n" test-pattern)))) (substitute* "schema_salad/tests/test_cg.py" (("^def test_(load(_by_yaml_metaschema|_metaschema|_cwlschema|)|include|idmap|idmap2)\\(" all) (skip-test all))) (substitute* "schema_salad/tests/test_cwl11.py" (("^def test_(secondaryFiles|outputBinding|yaml_tab_error)\\(" all) (skip-test all))) (substitute* "schema_salad/tests/test_examples.py" (("^def test_bad_schemas\\(" all) (skip-test all))))))))) (propagated-inputs (list python-cachecontrol python-importlib-resources python-mistune-next python-mypy-extensions python-rdflib python-requests python-ruamel.yaml)) (native-inputs (list python-black python-pytest python-pytest-runner python-pytest-xdist)) (home-page "https://github.com/common-workflow-language/schema_salad") (synopsis "Schema Annotations for Linked Avro Data (SALAD)") (description "Salad is a schema language for describing JSON or YAML structured linked data documents. Salad schema describes rules for preprocessing, structural validation, and hyperlink checking for documents described by a Salad schema. Salad supports rich data modeling with inheritance, template specialization, object identifiers, object references, documentation generation, code generation, and transformation to RDF. Salad provides a bridge between document and record oriented data modeling and the Semantic Web.") (license license:asl2.0))) (define-public python-scikit-bio (package (name "python-scikit-bio") (version "0.6.0") (source (origin (method url-fetch) (uri (pypi-uri "scikit-bio" version)) (sha256 (base32 "03y1n91p6m44hhxm3rpb355j6ddalydz49s94h85kbhm7iy5l40h")))) (build-system pyproject-build-system) (arguments (list #:test-flags ;; Accuracy problem '(list "-k" (string-append "not test_fisher_alpha" ;; UNEXPECTED EXCEPTION: ValueError("could ;; not convert string to float: 'gut'") " and not skbio.diversity")) #:phases '(modify-phases %standard-phases (add-before 'check 'build-extensions (lambda _ ;; Cython extensions have to be built before running the tests. (invoke "python3" "setup.py" "build_ext" "--inplace"))) (replace 'check (lambda* (#:key tests? test-flags #:allow-other-keys) (when tests? (apply invoke "python3" "-m" "skbio.test" test-flags))))))) (propagated-inputs (list python-biom-format python-decorator python-h5py python-hdmedians python-natsort python-numpy python-pandas python-requests python-scipy)) (native-inputs (list python-coverage python-pytest)) (home-page "https://scikit-bio.org") (synopsis "Data structures, algorithms and educational resources for bioinformatics") (description "This package provides data structures, algorithms and educational resources for bioinformatics.") (license license:bsd-3))) (define-public python-scrublet (package (name "python-scrublet") (version "0.2.3") (source (origin (method url-fetch) (uri (pypi-uri "scrublet" version)) (sha256 (base32 "0fk5pwk12yz9wpvwkl6j2l2g28f3x35b9r9n5bw6f0i9f0qgd191")))) (build-system pyproject-build-system) (arguments '(#:tests? #false)) ;there are none (propagated-inputs (list python-annoy python-cython python-matplotlib python-numba python-numpy python-pandas python-scikit-image python-scikit-learn python-scipy python-umap-learn)) (home-page "https://github.com/swolock/scrublet") (synopsis "Tool to indentify and remove doublets in single-cell data") (description "This package provides a tool for identifying and removing doublets in single-cell RNA-seq data.") (license license:expat))) (define-public python-cwlformat (package (name "python-cwlformat") (version "2022.02.18") (source ;; The PyPI tarball is missing Readme.md. Readme.md is required for the ;; build. (origin (method git-fetch) (uri (git-reference (url "https://github.com/rabix/cwl-format") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "0agkz2w86k91rc9m5vx5hsqi5nm6fcmzkng6j99hjapz0r9233ql")))) (build-system pyproject-build-system) (propagated-inputs (list python-importlib-resources python-ruamel.yaml)) (home-page "https://github.com/rabix/cwl-format") (synopsis "Prettifier for CWL code") (description "@code{python-cwlformat} is a specification and a reference implementation for a very opinionated @acronym{CWL, Common Workflow Language} code formatter. It outputs CWL in a standardized YAML format.") (license license:asl2.0))) (define-public python-cwl-upgrader (package (name "python-cwl-upgrader") (version "1.2.11") (source (origin (method url-fetch) (uri (pypi-uri "cwl-upgrader" version)) (sha256 (base32 "12j6z8nvwnzjjyypz59hwj5hmrcri2r6aknw52n9dbj6lbzbdd2p")))) (build-system pyproject-build-system) (native-inputs (list python-pytest)) (propagated-inputs (list python-ruamel.yaml python-schema-salad)) (home-page "https://github.com/common-workflow-language/cwl-upgrader") (synopsis "CWL document upgrader") (description "@code{python-cwl-upgrader} is a standalone upgrader for @acronym{CWL, Common Workflow Language} documents from version draft-3, v1.0, and v1.1 to v1.2.") (license license:asl2.0))) (define-public python-cwl-utils (package (name "python-cwl-utils") (version "0.32") (source (origin (method url-fetch) (uri (pypi-uri "cwl-utils" version)) (sha256 (base32 "06wkw8d8cqm3hnz8xwnysz874gwaym36c358cr7frw5iglhvsj98")))) (build-system pyproject-build-system) (arguments (list #:test-flags #~(list "-k" (string-append "not test_graph_split" " and not test_load_document_with_remote_uri" " and not test_remote_packing" " and not test_remote_packing_github_soft_links" " and not test_value_from_two_concatenated_expressions")))) (inputs (list node)) (native-inputs (list python-mypy-extensions python-pytest python-pytest-mock python-pytest-runner)) (propagated-inputs (list python-cwl-upgrader python-cwlformat python-packaging python-rdflib python-requests python-ruamel.yaml python-schema-salad)) (home-page "https://github.com/common-workflow-language/cwl-utils") (synopsis "Python utilities for CWL") (description "@code{python-cwl-utils} provides python utilities and autogenerated classes for loading and parsing CWL v1.0, CWL v1.1, and CWL v1.2 documents.") (license license:asl2.0))) (define-public cwltool (package (name "cwltool") (version "3.1.20240112164112") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/common-workflow-language/cwltool") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "1fpc5kqgpbn48g5vlvy64p297x2wm3gfz8casgpk15ap593wwh33")))) (build-system pyproject-build-system) (arguments (list #:phases #~(modify-phases %standard-phases (add-after 'unpack 'loosen-version-restrictions (lambda _ (substitute* "setup.py" (("== 1.5.1") "> 1.5.1")))) ; prov (add-after 'unpack 'set-version (lambda _ ;; Set exact version. (substitute* "setup.py" (("use_scm_version=True") (string-append "version=\"" #$version "\""))))) (add-after 'unpack 'modify-tests (lambda _ ;; Tries to connect to the internet. (delete-file "tests/test_content_type.py") (delete-file "tests/test_udocker.py") (delete-file "tests/test_http_input.py") (substitute* "tests/test_load_tool.py" (("def test_load_graph_fragment_from_packed") (string-append "@pytest.mark.skip(reason=\"Disabled by Guix\")\n" "def test_load_graph_fragment_from_packed"))) (substitute* "tests/test_examples.py" (("def test_env_filtering") (string-append "@pytest.mark.skip(reason=\"Disabled by Guix\")\n" "def test_env_filtering"))) ;; Tries to use cwl-runners. (substitute* "tests/test_examples.py" (("def test_v1_0_arg_empty_prefix_separate_false") (string-append "@pytest.mark.skip(reason=\"Disabled by Guix\")\n" "def test_v1_0_arg_empty_prefix_separate_false"))) (substitute* '("tests/subgraph/env-tool2.cwl" "tests/subgraph/env-tool2_req.cwl" "tests/subgraph/env-wf2_subwf-packed.cwl" "tests/subgraph/env-tool2_no_env.cwl") (("\"/bin/sh\"") (string-append "\"" (which "sh") "\"")))))))) (inputs (list python-argcomplete python-bagit python-coloredlogs python-cwl-utils python-mypy-extensions python-prov python-pydot python-psutil python-rdflib python-requests python-ruamel.yaml python-schema-salad python-shellescape python-spython python-typing-extensions ;; Not listed as needed but still necessary: node)) (native-inputs (list python-arcp python-humanfriendly python-mock python-pytest python-pytest-cov python-pytest-mock python-pytest-runner python-pytest-xdist)) (home-page "https://github.com/common-workflow-language/common-workflow-language") (synopsis "Common Workflow Language reference implementation") (description "This is the reference implementation of the @acronym{CWL, Common Workflow Language} standards. The CWL open standards are for describing analysis workflows and tools in a way that makes them portable and scalable across a variety of software and hardware environments, from workstations to cluster, cloud, and high performance computing (HPC) environments. CWL is designed to meet the needs of data-intensive science, such as Bioinformatics, Medical Imaging, Astronomy, Physics, and Chemistry. The @acronym{cwltool, CWL reference implementation} is intended to be feature complete and to provide comprehensive validation of CWL files as well as provide other tools related to working with CWL descriptions.") (license license:asl2.0))) (define-public python-dendropy (package (name "python-dendropy") (version "4.5.1") (source (origin (method git-fetch) ;; Source from GitHub so that tests are included. (uri (git-reference (url "https://github.com/jeetsukumaran/DendroPy") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "0lrfzjqzbpk1rrra9vd7z2j7q09jy9w1ss7wn2rd85i4k5y3xz8l")))) (build-system pyproject-build-system) (arguments (list #:test-flags '(list "-k" (string-join ;; These tests fail because we have no "paup" executable. (list "not test_group1" "test_basic_split_counting_under_different_rootings" "test_basic_split_count_with_incorrect_weight_treatment_raises_error" "test_basic_split_count_with_incorrect_rootings_raises_error" ;; Assert error for unknown reasons "test_by_num_lineages") " and not ")) #:phases '(modify-phases %standard-phases (add-after 'unpack 'python-compatibility (lambda _ (substitute* "tests/test_datamodel_taxon.py" (("collections.Iterable") "collections.abc.Iterable"))))))) (native-inputs (list python-pytest)) (home-page "https://dendropy.org/") (synopsis "Library for phylogenetics and phylogenetic computing") (description "DendroPy is a library for phylogenetics and phylogenetic computing: reading, writing, simulation, processing and manipulation of phylogenetic trees (phylogenies) and characters.") (license license:bsd-3))) (define-public python-py2bit (package (name "python-py2bit") (version "0.3.0") (source (origin (method url-fetch) (uri (pypi-uri "py2bit" version)) (sha256 (base32 "1vw2nvw1yrl7ikkqsqs1pg239yr5nspvd969r1x9arms1k25a1a5")))) (build-system python-build-system) (home-page "https://github.com/dpryan79/py2bit") (synopsis "Access 2bit files using lib2bit") (description "This package provides Python bindings for lib2bit to access 2bit files with Python.") (license license:expat))) (define-public delly (package (name "delly") (version "0.8.3") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/dellytools/delly") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "1ibnplgfzj96w8glkx17v7sld3pm402fr5ybmf3h0rlcryabxrqy")) (modules '((guix build utils))) (snippet '(delete-file-recursively "src/htslib")))) (build-system gnu-build-system) (arguments (list #:tests? #f ;There are no tests to run. #:make-flags #~(list "PARALLEL=1" ; Allow parallel execution at run-time. (string-append "prefix=" #$output)) #:phases #~(modify-phases %standard-phases (delete 'configure) ; There is no configure phase. (add-after 'install 'install-templates (lambda _ (let ((templates (string-append #$output "/share/delly/templates"))) (mkdir-p templates) (copy-recursively "excludeTemplates" templates))))))) (inputs (list boost bzip2 htslib zlib)) (home-page "https://github.com/dellytools/delly") (synopsis "Integrated structural variant prediction method") (description "Delly is an integrated structural variant prediction method that can discover and genotype deletions, tandem duplications, inversions and translocations at single-nucleotide resolution in short-read massively parallel sequencing data. It uses paired-ends and split-reads to sensitively and accurately delineate genomic rearrangements throughout the genome.") (license license:gpl3+))) (define-public transanno (package (name "transanno") (version "0.3.0") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/informationsea/transanno") ;; Corresponds to tag v0.3.0 (commit "df49050c92644ea12d9d5c6fae2186ca436dbca3"))) (file-name (git-file-name name version)) (sha256 (base32 "1jpn7s3cnd9ybk4lmfbhj2arhf6cmrv7jp74n7n87m3a3irkaif1")) (snippet '(with-output-to-file "liftover-rs/build.rs" (lambda _ (format #true "fn main() {~@ println!(\"cargo:rustc-link-lib=lzma\");~@ }~%")))))) (build-system cargo-build-system) (arguments (list #:install-source? #false ;fails #:phases #~(modify-phases %standard-phases (add-after 'unpack 'prepare-test-files (lambda _ (delete-file "Cargo.lock") (substitute* "liftover-rs/prepare-test.sh" (("/bin/bash") (string-append #$(this-package-native-input "bash") "/bin/bash"))) (invoke "bash" "prepare-test-files.sh"))) (add-before 'install 'chdir (lambda _ (chdir "transanno")))) #:cargo-inputs `(("rust-anyhow" ,rust-anyhow-1) ("rust-autocompress" ,rust-autocompress-0.2) ("rust-bio" ,rust-bio-0.41) ("rust-clap" ,rust-clap-2) ("rust-csv" ,rust-csv-1) ("rust-flate2" ,rust-flate2-1) ("rust-indexmap" ,rust-indexmap-1) ("rust-log" ,rust-log-0.4) ("rust-nom" ,rust-nom-5) ("rust-once-cell" ,rust-once-cell-1) ("rust-pretty-env-logger" ,rust-pretty-env-logger-0.3) ("rust-regex" ,rust-regex-1) ("rust-thiserror" ,rust-thiserror-1) ("rust-serde" ,rust-serde-1) ("rust-serde-json" ,rust-serde-json-1)) #:cargo-development-inputs `(("rust-clap" ,rust-clap-2) ("rust-lazy-static" ,rust-lazy-static-1)))) (native-inputs (list bash pkg-config)) (inputs (list xz)) (home-page "https://github.com/informationsea/transanno") (synopsis "LiftOver tool for new genome assemblies") (description "This package provides an accurate VCF/GFF3/GTF LiftOver tool for new genome assemblies.") (license license:gpl3+))) (define-public trf (package (name "trf") (version "4.09.1") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/Benson-Genomics-Lab/TRF") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "0fhwr4s1mf8nw8fr5imwjvjr42b59p97zr961ifm8xl1bajz4wpg")))) (build-system gnu-build-system) (home-page "https://github.com/Benson-Genomics-Lab/TRF") (synopsis "Tandem Repeats Finder: a program to analyze DNA sequences") (description "A tandem repeat in DNA is two or more adjacent, approximate copies of a pattern of nucleotides. Tandem Repeats Finder is a program to locate and display tandem repeats in DNA sequences. In order to use the program, the user submits a sequence in FASTA format. The output consists of two files: a repeat table file and an alignment file. Submitted sequences may be of arbitrary length. Repeats with pattern size in the range from 1 to 2000 bases are detected.") (license license:agpl3+))) (define-public trinityrnaseq (package (name "trinityrnaseq") (version "2.13.2") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/trinityrnaseq/trinityrnaseq.git") (commit (string-append "Trinity-v" version)) (recursive? #true))) (file-name (git-file-name name version)) (sha256 (base32 "1qszrxqbx4q5pavpgm4rkrh1z1v1mf7qx83vv3fnlqdmncnsf1gv")))) (build-system gnu-build-system) (arguments (list #:test-target "test" #:modules '((guix build gnu-build-system) (guix build utils) (ice-9 match) (srfi srfi-1)) #:make-flags #~(list (string-append "CC=" #$(cc-for-target))) #:phases #~(modify-phases %standard-phases (replace 'configure (lambda _ (setenv "SHELL" (which "sh")) (setenv "CONFIG_SHELL" (which "sh")) ;; Do not require version.h, which triggers a local build of a ;; vendored htslib. (substitute* "trinity-plugins/bamsifter/Makefile" (("sift_bam_max_cov.cpp htslib/version.h") "sift_bam_max_cov.cpp")))) (add-after 'build 'build-plugins (lambda _ ;; Run this in the subdirectory to avoid running the ;; tests right here. (with-directory-excursion "trinity-plugins" (invoke "make" "plugins")))) ;; The install script uses rsync, provides no overrides for the ;; default location at /usr/local/bin, and patching it would change ;; all lines that do something. (replace 'install (lambda* (#:key inputs #:allow-other-keys) (let ((share (string-append #$output "/share/trinity/")) (bin (string-append #$output "/bin/"))) (mkdir-p bin) (copy-recursively "." share) (delete-file (string-append share "/Chrysalis/build/CMakeFiles/CMakeOutput.log")) (delete-file (string-append share "/Inchworm/build/CMakeFiles/CMakeOutput.log")) (wrap-program (string-append share "Trinity") `("R_LIBS_SITE" ":" = (,(getenv "R_LIBS_SITE"))) `("PERL5LIB" ":" = (,(getenv "PERL5LIB"))) `("PYTHONPATH" ":" = (,(getenv "GUIX_PYTHONPATH"))) `("PATH" ":" = ,(cons (string-append share "/trinity-plugins/BIN") (filter-map (match-lambda ((name . dir) (string-append dir "/bin"))) inputs)))) (symlink (string-append share "Trinity") (string-append bin "Trinity")))))))) (inputs (list blast+ bowtie fastqc hisat htslib icedtea-8 jellyfish kallisto multiqc perl perl-uri-escape python-numpy python-wrapper r-ape r-argparse r-biobase r-ctc r-deseq2 r-edger r-fastcluster r-glimma r-goplot r-goseq r-gplots r-minimal r-qvalue r-rots r-sm r-tidyverse rsem salmon samtools sra-tools star zlib)) (propagated-inputs (list coreutils gzip which)) (native-inputs (list cmake)) (home-page "https://github.com/trinityrnaseq/trinityrnaseq/wiki") (synopsis "Trinity RNA-Seq de novo transcriptome assembly") (description "Trinity assembles transcript sequences from Illumina RNA-Seq data. Trinity represents a novel method for the efficient and robust de novo reconstruction of transcriptomes from RNA-seq data. Trinity combines three independent software modules: Inchworm, Chrysalis, and Butterfly, applied sequentially to process large volumes of RNA-seq reads. Trinity partitions the sequence data into many individual de Bruijn graphs, each representing the transcriptional complexity at a given gene or locus, and then processes each graph independently to extract full-length splicing isoforms and to tease apart transcripts derived from paralogous genes.") (license license:bsd-3))) (define-public repeat-masker (package (name "repeat-masker") (version "4.1.2-p1") (source (origin (method url-fetch) (uri (string-append "http://www.repeatmasker.org/" "RepeatMasker/RepeatMasker-" version ".tar.gz")) (sha256 (base32 "15hfdfpzmdjcx7ng7rjfid69bmvgn3z9g9r43qhjnhjhq3v4prab")))) (build-system gnu-build-system) (arguments `(#:tests? #false ; there are none #:phases (modify-phases %standard-phases (delete 'configure) (replace 'build (lambda* (#:key inputs outputs #:allow-other-keys) (let ((share (string-append (assoc-ref outputs "out") "/share/RepeatMasker"))) (mkdir-p share) (copy-recursively "." share) (with-directory-excursion share (invoke "perl" "configure" "--trf_prgm" (which "trf") "--hmmer_dir" (string-append (assoc-ref inputs "hmmer") "/bin")))))) (replace 'install (lambda* (#:key outputs #:allow-other-keys) (let* ((out (assoc-ref outputs "out")) (share (string-append out "/share/RepeatMasker")) (bin (string-append out "/bin")) (path (getenv "PERL5LIB"))) (install-file (string-append share "/RepeatMasker") bin) (wrap-program (string-append bin "/RepeatMasker") `("PERL5LIB" ":" prefix (,path ,share))))))))) (inputs (list bash-minimal perl perl-text-soundex python python-h5py hmmer trf)) (home-page "https://github.com/Benson-Genomics-Lab/TRF") (synopsis "Tandem Repeats Finder: a program to analyze DNA sequences") (description "A tandem repeat in DNA is two or more adjacent, approximate copies of a pattern of nucleotides. Tandem Repeats Finder is a program to locate and display tandem repeats in DNA sequences. In order to use the program, the user submits a sequence in FASTA format. The output consists of two files: a repeat table file and an alignment file. Submitted sequences may be of arbitrary length. Repeats with pattern size in the range from 1 to 2000 bases are detected.") (license license:osl2.1))) (define-public trust4 (package (name "trust4") (version "1.1.0") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/liulab-dfci/TRUST4") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "170k4rrchg7f2jyn3v4y4fxxq1d49n1vnvhx5xcnnr6jql8q3h08")) (modules '((guix build utils))) (snippet '(begin ;; Remove bundled samtools (delete-file-recursively "samtools-0.1.19"))))) (build-system gnu-build-system) (arguments (list #:tests? #f ;there are no tests #:phases #~(modify-phases %standard-phases (add-after 'unpack 'use-samtools-headers (lambda* (#:key inputs #:allow-other-keys) (substitute* "Makefile" (("LINKPATH= -I./samtools-0.1.19 -L./samtools-0.1.19") (string-append "LINKPATH= -I." #$(this-package-native-input "samtools") "/include/samtools" " -L." #$(this-package-native-input "samtools") "/lib")) (("./samtools-0.1.19/") (string-append #$(this-package-native-input "samtools") "/lib/"))) (substitute* "alignments.hpp" (("samtools-0.1.19") (string-append #$(this-package-native-input "samtools") "/include/samtools"))))) (delete 'configure) ; No configure. (replace 'install (lambda* (#:key outputs #:allow-other-keys) (let ((bin (string-append (assoc-ref outputs "out") "/bin")) (scripts (string-append #$output "/share/trust4/scripts"))) (install-file "annotator" bin) (install-file "bam-extractor" bin) (install-file "fastq-extractor" bin) (install-file "run-trust4" bin) (install-file "trust4" bin) ;; install scripts stored in the scrips dir (for-each (lambda (file) (chmod file #o555)) (find-files "scripts" "\\.p(y|l)")) (copy-recursively "scripts" scripts) (delete-file-recursively "scripts") ;; install the rest of the scripts that are in the main dir (for-each (lambda (file) (chmod file #o555) (install-file file bin)) (find-files "." "\\.(pl|py|sh)")))))))) (native-inputs (list automake samtools-0.1)) (inputs (list perl python-wrapper zlib)) (home-page "https://github.com/liulab-dfci/TRUST4") (synopsis "TCR and BCR assembly from RNA-seq data") (description "This package is analyzing @acronym{TCR, T cell receptor} and @acronym{BCR, B cell receptor} sequences using unselected RNA sequencing data, profiled from fluid and solid tissues, including tumors. TRUST4 performs de novo assembly on V, J, C genes including the hypervariable @acronym{CDR3, complementarity-determining region 3} and reports consensus contigs of BCR/TCR sequences. TRUST4 then realigns the contigs to IMGT reference gene sequences to identify the corresponding gene and CDR3 details. TRUST4 supports both single-end and paired-end bulk or single-cell sequencing data with any read length.") (license license:gpl3))) (define-public diamond (package (name "diamond") (version "2.1.6") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/bbuchfink/diamond") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "0kb17jwlsrvgswfahzznrffv1i6ybwwmq99qs7iga5yzbx64jp6q")))) (build-system cmake-build-system) (arguments (list #:configure-flags '(list "-DX86=OFF"))) ;avoid SSE4 and AVX2 (inputs (list zlib)) (home-page "https://github.com/bbuchfink/diamond") (synopsis "Accelerated BLAST compatible local sequence aligner") (description "DIAMOND is a BLAST-compatible local aligner for mapping protein and translated DNA query sequences against a protein reference database (BLASTP and BLASTX alignment mode). The speedup over BLAST is up to 20,000 on short reads at a typical sensitivity of 90-99% relative to BLAST depending on the data and settings.") (license license:gpl3+))) (define-public discrover (package (name "discrover") (version "1.6.0") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/maaskola/discrover") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "173fwi2vb6a5kp406hm3jj6j7v4whww796f2qcygp4rpvamh307y")))) (build-system cmake-build-system) (arguments `(#:tests? #f ; there are no tests #:phases (modify-phases %standard-phases (add-before 'build 'set-force-source-date ;; for reproducible dates, texlive needs this to respect ;; SOURCE_DATE_EPOCH (lambda _ (setenv "FORCE_SOURCE_DATE" "1"))) (add-after 'unpack 'fix-latex-errors (lambda _ (with-fluids ((%default-port-encoding #f)) (substitute* "doc/references.bib" (("\\{S\\}illanp[^,]+,") "{S}illanp{\\\"a}{\\\"a},"))) ;; XXX: I just can't get pdflatex to not complain about these ;; characters. They end up in the manual via the generated ;; discrover-cli-help.txt. (substitute* "src/hmm/cli.cpp" (("µ") "mu") (("η") "eta") (("≤") "<=")) ;; This seems to be a syntax error. (substitute* "doc/discrover-manual.tex" (("theverbbox\\[t\\]") "theverbbox")))) (add-after 'unpack 'add-missing-includes (lambda _ (substitute* "src/executioninformation.hpp" (("#define EXECUTIONINFORMATION_HPP" line) (string-append line "\n#include <random>"))) (substitute* "src/plasma/fasta.hpp" (("#define FASTA_HPP" line) (string-append line "\n#include <random>")))))))) (inputs (list boost cairo rmath-standalone)) (native-inputs (list (texlive-updmap.cfg (list texlive-doi texlive-examplep texlive-forloop texlive-listofitems texlive-ms texlive-natbib texlive-pgf ;tikz texlive-readarray texlive-verbatimbox)) imagemagick)) (home-page "https://dorina.mdc-berlin.de/public/rajewsky/discrover/") (synopsis "Discover discriminative nucleotide sequence motifs") (description "Discrover is a motif discovery method to find binding sites of nucleic acid binding proteins.") (license license:gpl3+))) (define-public eigensoft (package (name "eigensoft") (version "7.2.1") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/DReichLab/EIG") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "1c141fqvhnzibmnf22sv23vbmzm20kjjyrib44cfh75wyndp2d9k")) (modules '((guix build utils))) ;; Remove pre-built binaries. (snippet '(begin (delete-file-recursively "bin") (mkdir "bin") #t)))) (build-system gnu-build-system) (arguments `(#:tests? #f ; There are no tests. #:make-flags '("CC=gcc") #:phases (modify-phases %standard-phases ;; There is no configure phase, but the Makefile is in a ;; sub-directory. (replace 'configure (lambda _ (chdir "src") #t)) ;; The provided install target only copies executables to ;; the "bin" directory in the build root. (add-after 'install 'actually-install (lambda* (#:key outputs #:allow-other-keys) (let* ((out (assoc-ref outputs "out")) (bin (string-append out "/bin"))) (for-each (lambda (file) (install-file file bin)) (find-files "../bin" ".*")) #t)))))) (inputs (list gsl openblas perl `(,gfortran "lib"))) (home-page "https://github.com/DReichLab/EIG") (synopsis "Tools for population genetics") (description "The EIGENSOFT package provides tools for population genetics and stratification correction. EIGENSOFT implements methods commonly used in population genetics analyses such as PCA, computation of Tracy-Widom statistics, and finding related individuals in structured populations. It comes with a built-in plotting script and supports multiple file formats and quantitative phenotypes.") ;; The license of the eigensoft tools is Expat, but since it's ;; linking with the GNU Scientific Library (GSL) the effective ;; license is the GPL. (license license:gpl3+))) (define-public eddylab-squid (package (name "eddylab-squid") (version "1.9g") (source (origin (method url-fetch) (uri (string-append "http://eddylab.org/software/squid/squid-" version ".tar.gz")) (sha256 (base32 "19ywv1h581a84yyjnp64gwww99vhgbxi8v4rl37xp92ag7l44brh")))) (build-system gnu-build-system) (arguments `(#:phases (modify-phases %standard-phases (add-before 'check 'set-perl-search-path (lambda _ ;; Work around "dotless @INC" build failure. (setenv "PERL5LIB" (string-append (getcwd) "/Testsuite:" (getenv "PERL5LIB")))))))) (inputs (list perl)) (home-page "http://eddylab.org/software.html") (synopsis "C function library for sequence analysis") (description "SQUID is Sean Eddy's personal library of C functions and utility programs for sequence analysis.") (license license:gpl2))) (define-public edirect (package (name "edirect") (version "13.3.20200128") (source (origin (method url-fetch) (uri (string-append "ftp://ftp.ncbi.nlm.nih.gov/entrez/entrezdirect" "/versions/" version "/edirect-" version ".tar.gz")) (sha256 (base32 "093zp7klv81ph0y8mm8d78a9hnpfxbv2kdym70gzdf3vz176rw33")) (modules '((guix build utils))) (snippet '(begin (delete-file "Mozilla-CA.tar.gz") (substitute* "rchive.go" ;; This go library does not have any license. (("github.com/fiam/gounidecode/unidecode") "golang.org/rainycape/unidecode")))))) (build-system perl-build-system) (arguments `(#:phases (modify-phases %standard-phases (delete 'configure) (delete 'build) (delete 'check) ; simple check after install (add-after 'unpack 'patch-programs (lambda* (#:key inputs #:allow-other-keys) ;; Ignore errors about missing xtract.Linux and rchive.Linux. (substitute* "pm-refresh" (("cat \\\"\\$target") "grep ^[[:digit:]] \"$target")))) (replace 'install (lambda* (#:key inputs outputs #:allow-other-keys) (let ((bin (string-append (assoc-ref outputs "out") "/bin")) (edirect-go (assoc-ref inputs "edirect-go-programs"))) (for-each (lambda (file) (install-file file bin)) '("archive-pubmed" "asp-cp" "asp-ls" "download-ncbi-data" "download-pubmed" "edirect.pl" "efetch" "epost" "esearch" "fetch-pubmed" "ftp-cp" "ftp-ls" "has-asp" "index-pubmed" "pm-prepare" "pm-refresh" "pm-stash" "pm-collect" "pm-index" "pm-invert" "pm-merge" "pm-promote")) (symlink (string-append edirect-go "/bin/xtract.Linux") (string-append bin "/xtract")) (symlink (string-append edirect-go "/bin/rchive.Linux") (string-append bin "/rchive"))))) (add-after 'install 'wrap-program (lambda* (#:key outputs #:allow-other-keys) ;; Make sure everything can run in a pure environment. (let ((out (assoc-ref outputs "out")) (path (getenv "PERL5LIB"))) (for-each (lambda (file) (wrap-program file `("PERL5LIB" ":" prefix (,path))) (wrap-program file `("PATH" ":" prefix (,(string-append out "/bin") ,(dirname (which "sed")) ,(dirname (which "gzip")) ,(dirname (which "grep")) ,(dirname (which "perl")) ,(dirname (which "uname")))))) (find-files out "."))))) (add-after 'wrap-program 'check (lambda* (#:key outputs #:allow-other-keys) (invoke (string-append (assoc-ref outputs "out") "/bin/edirect.pl") "-filter" "-help")))))) (inputs (list bash-minimal edirect-go-programs perl-html-parser perl-encode-locale perl-file-listing perl-html-tagset perl-html-tree perl-http-cookies perl-http-date perl-http-message perl-http-negotiate perl-lwp-mediatypes perl-lwp-protocol-https perl-net-http perl-uri perl-www-robotrules perl-xml-simple perl)) (home-page "https://www.ncbi.nlm.nih.gov/books/NBK179288/") (synopsis "Tools for accessing the NCBI's set of databases") (description "Entrez Direct (EDirect) is a method for accessing the National Center for Biotechnology Information's (NCBI) set of interconnected databases (publication, sequence, structure, gene, variation, expression, etc.) from a terminal. Functions take search terms from command-line arguments. Individual operations are combined to build multi-step queries. Record retrieval and formatting normally complete the process. EDirect also provides an argument-driven function that simplifies the extraction of data from document summaries or other results that are returned in structured XML format. This can eliminate the need for writing custom software to answer ad hoc questions.") (native-search-paths ;; Ideally this should be set for LWP somewhere. (list (search-path-specification (variable "PERL_LWP_SSL_CA_FILE") (file-type 'regular) (separator #f) (files '("/etc/ssl/certs/ca-certificates.crt"))))) (license license:public-domain))) (define-public edirect-go-programs (package (inherit edirect) (name "edirect-go-programs") (build-system go-build-system) (arguments `(#:install-source? #f #:tests? #f ; No tests. #:import-path "ncbi.nlm.nih.gov/entrez/edirect" #:phases (modify-phases %standard-phases (replace 'build (lambda* (#:key import-path #:allow-other-keys) (with-directory-excursion (string-append "src/" import-path) (invoke "go" "build" "-v" "-x" "j2x.go") (invoke "go" "build" "-v" "-x" "t2x.go") (invoke "go" "build" "-v" "-x" "-o" "xtract.Linux" "xtract.go" "common.go") (invoke "go" "build" "-v" "-x" "-o" "rchive.Linux" "rchive.go" "common.go") (invoke "go" "build" "-v" "-x" "-o" "symbols.Linux" "s2p.go")))) (replace 'install (lambda* (#:key outputs import-path #:allow-other-keys) (let ((dest (string-append (assoc-ref outputs "out") "/bin")) (source (string-append "src/" import-path "/"))) (for-each (lambda (file) (format #t "installing ~a~%" file) (install-file (string-append source file) dest)) '("j2x" "t2x" "symbols.Linux" "xtract.Linux" "rchive.Linux")) #t)))))) (native-inputs '()) (propagated-inputs '()) (inputs (list go-github-com-fatih-color go-github-com-fogleman-gg go-github-com-gedex-inflector go-github-com-golang-freetype go-github-com-klauspost-cpuid go-github-com-pbnjay-memory go-github-com-surgebase-porter2 go-golang-org-rainycape-unidecode go-golang-org-x-image go-golang-org-x-text)))) (define-public python-baltica (package (name "python-baltica") (version "1.1.2") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/dieterich-lab/Baltica") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "001ac03v9pbqqzf9pv7v8gf0296ksa4f0v3wdmpa6m9701skqi4r")))) (build-system pyproject-build-system) (arguments (list #:phases '(modify-phases %standard-phases (replace 'check (lambda* (#:key tests? #:allow-other-keys) (when tests? ;; The tests need to be run from elsewhere... (mkdir-p "/tmp/test") (copy-recursively ".tests" "/tmp/test") (with-directory-excursion "/tmp/test" (invoke "pytest" "-v" "--doctest-modules")))))))) (propagated-inputs (list gunicorn python-anndata python-click python-flask python-flask-wtf python-h5py python-numpy python-psutil python-pysam python-pyyaml python-scipy r-biocmanager r-dplyr r-genomicranges r-here r-openxlsx r-optparse r-readr r-rsamtools r-stringr r-tidyr r-upsetr r-yaml snakemake-7)) (native-inputs (list python-cython python-pyfakefs python-pytest)) (home-page "https://github.com/dieterich-lab/Baltica") (synopsis "Integrated splice junction usage analysis") (description "This framework facilitates the execution of @dfn{differential junction usage} (DJU) methods. Additionally, it enables the integration of results from multiple DJU methods.") (license license:expat))) (define-public python-bamnostic (package (name "python-bamnostic") (version "1.1.8") (source (origin (method url-fetch) (uri (pypi-uri "bamnostic" version)) (sha256 (base32 "0cjpzyqz6r4lmiwry2gcxdczwpkhl3lyyjg4s8addln17691ysxk")))) (build-system pyproject-build-system) (propagated-inputs (list python-pytest)) (home-page "https://github.com/betteridiot/bamnostic/") (synopsis "Tool for binary alignment map, random access and parsing") (description "Bamnostic is a pure Python @dfn{Binary Alignment Map} (BAM) file parser and random access tool.") (license license:bsd-3))) (define-public python-episcanpy (package (name "python-episcanpy") (version "0.4.0") (source (origin (method url-fetch) (uri (pypi-uri "episcanpy" version)) (sha256 (base32 "1qqcyhyzy6idpjmidfdpzwk02hbxm25rymz42h51nlk0vd4r2wwm")))) (build-system pyproject-build-system) (arguments (list ;; The tests import episcanpy.api, but this is known to not work. ;; See https://github.com/colomemaria/epiScanpy/issues/133 #:tests? #false #:phases '(modify-phases %standard-phases ;; Numba needs a writable dir to cache functions. (add-before 'build 'set-numba-cache-dir (lambda _ (setenv "NUMBA_CACHE_DIR" "/tmp")))))) (propagated-inputs (list python-anndata python-bamnostic python-h5py python-intervaltree python-joblib python-kneed python-legacy-api-wrap python-matplotlib python-natsort python-networkx python-numba python-numpy python-packaging python-pandas python-scanpy python-scikit-learn python-scipy python-seaborn python-statsmodels python-tqdm python-pysam python-tbb python-umap-learn)) (native-inputs (list python-pytest python-setuptools-scm)) (home-page "https://github.com/colomemaria/epiScanpy") (synopsis "Tool for epigenomics single cell analysis") (description "EpiScanpy is a toolkit to analyse single-cell open chromatin (scATAC-seq) and single-cell DNA methylation (for example scBS-seq) data. EpiScanpy is the epigenomic extension of the very popular scRNA-seq analysis tool Scanpy (Genome Biology, 2018).") (license license:bsd-3))) (define-public python-ete3 (package (name "python-ete3") (version "3.1.3") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/etetoolkit/ete") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "1i6533wsm06mz0sdrisqai929j744cnczwjgsmxl847q5k16kngd")))) (build-system pyproject-build-system) (arguments (list #:test-flags '(list "-k" ;; This test crashes Python in the build container (string-append "not test_renderer" ;; These all need internet access " and not test_00_update_database" " and not test_01tree_annotation" " and not test_get_topology" " and not test_merged_id" " and not test_ncbi_compare" " and not test_ncbiquery") "ete3/test/test_api.py"))) (propagated-inputs (list python-lxml python-numpy python-pyqt python-scipy)) (native-inputs (list python-pytest)) (home-page "http://etetoolkit.org") (synopsis "Python environment for phylogenetic tree exploration") (description "This package provides a Python environment for phylogenetic tree exploration.") (license license:gpl3+))) (define-public python-illumina-utils (package (name "python-illumina-utils") (version "2.12") (source (origin (method url-fetch) (uri (pypi-uri "illumina-utils" version)) (sha256 (base32 "0z9g0prj7pmgl5z4vdpxv3v30grzhc194801qnf0wqzgy7w3aj2s")))) (build-system pyproject-build-system) (arguments (list #:tests? #false)) ;there are none (propagated-inputs (list python-matplotlib python-numpy python-levenshtein)) (home-page "https://github.com/meren/illumina-utils") (synopsis "Library and scripts to work with Illumina paired-end data") (description "This package provides a library and collection of scripts to work with Illumina paired-end data (for CASAVA 1.8+).") (license license:gpl2+))) (define-public python-pyani (package (name "python-pyani") (version "0.2.12") (source (origin (method url-fetch) (uri (pypi-uri "pyani" version)) (sha256 (base32 "124kdg7168nbh4a5wisfws1fgkd89dd4js9v6dml2lvgclbv4mjg")))) (build-system pyproject-build-system) ;; This contains two test data files but no way to run the tests. (arguments (list #:tests? #false)) (propagated-inputs (list python-biopython python-matplotlib python-pandas python-scipy python-seaborn)) (home-page "https://widdowquinn.github.io/pyani/") (synopsis "Calculate genome-scale average nucleotide identity") (description "Pyani provides a package and script for calculation of genome-scale average nucleotide identity.") (license license:expat))) (define-public python-pyahocorasick (package (name "python-pyahocorasick") (version "2.1.0") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/WojciechMula/pyahocorasick") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "1fsnivwcw56q7lwz41c5kbfvxv0v17mmkx43i2a293l49fxj08j8")))) (build-system pyproject-build-system) (native-inputs (list python-pytest python-twine python-wheel)) (home-page "https://github.com/WojciechMula/pyahocorasick") (synopsis "Library for finding multiple key strings in text") (description "Pyahocorasick is a fast, memory-efficient library for multi-pattern string search. This means that you can find multiple key strings occurrences at once in some input text.") (license license:bsd-3))) (define-public exonerate (package (name "exonerate") (version "2.4.0") (source (origin (method url-fetch) (uri (string-append "http://ftp.ebi.ac.uk/pub/software/vertebrategenomics/exonerate/" "exonerate-" version ".tar.gz")) (sha256 (base32 "0hj0m9xygiqsdxvbg79wq579kbrx1mdrabi2bzqz2zn9qwfjcjgq")))) (build-system gnu-build-system) (arguments `(#:parallel-build? #f)) ; Building in parallel fails on some machines. (native-inputs (list pkg-config)) (inputs (list glib)) (home-page "https://www.ebi.ac.uk/about/vertebrate-genomics/software/exonerate") (synopsis "Generic tool for biological sequence alignment") (description "Exonerate is a generic tool for pairwise sequence comparison. It allows the alignment of sequences using a many alignment models, either exhaustive dynamic programming or a variety of heuristics.") (license license:gpl3))) (define-public express (package (name "express") (version "1.5.3") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/adarob/eXpress") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "18nb22n7x820fzjngf4qgyb3mspqkw7xyk7v7s5ps6wfrd8qwscb")))) (build-system cmake-build-system) (arguments (list #:tests? #f ;no "check" target #:phases #~(modify-phases %standard-phases (add-after 'unpack 'use-shared-boost-libs-and-set-bamtools-paths (lambda* (#:key inputs #:allow-other-keys) (substitute* "CMakeLists.txt" (("set\$Boost_USE_STATIC_LIBS ON\$") "set(Boost_USE_STATIC_LIBS OFF)") (("\\$\\{CMAKE_CURRENT_SOURCE_DIR\\}/bamtools/include") (search-input-directory inputs "/include/bamtools")) (("\\$\\{PROJECT_SOURCE_DIR\\}/bamtools/lib/libbamtools.a") (search-input-file inputs "/lib/libbamtools.so")) (("libbamtools.a") "libbamtools.so")) (substitute* "src/CMakeLists.txt" (("libprotobuf.a") "libprotobuf.so")))) (add-after 'unpack 'remove-update-check (lambda _ (substitute* "src/main.cpp" (("#include \"update_check.h\"") "") (("check_version\$PACKAGE_VERSION\$;") ""))))))) (inputs (list boost bamtools protobuf zlib)) (home-page "http://bio.math.berkeley.edu/eXpress") (synopsis "Streaming quantification for high-throughput genomic sequencing") (description "eXpress is a streaming tool for quantifying the abundances of a set of target sequences from sampled subsequences. Example applications include transcript-level RNA-Seq quantification, allele-specific/haplotype expression analysis (from RNA-Seq), transcription factor binding quantification in ChIP-Seq, and analysis of metagenomic data.") (license license:artistic2.0))) (define-public express-beta-diversity (package (name "express-beta-diversity") (version "1.0.8") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/dparks1134/ExpressBetaDiversity") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "0s0yzg5c21349rh7x4w9266jsvnp7j1hp9cf8sk32hz8nvrj745x")))) (build-system gnu-build-system) (arguments `(#:phases (modify-phases %standard-phases (delete 'configure) (add-before 'build 'enter-source (lambda _ (chdir "source") #t)) (replace 'check (lambda _ (invoke "../bin/ExpressBetaDiversity" "-u") #t)) (replace 'install (lambda* (#:key outputs #:allow-other-keys) (let ((bin (string-append (assoc-ref outputs "out") "/bin"))) (install-file "../scripts/convertToEBD.py" bin) (install-file "../bin/ExpressBetaDiversity" bin) #t)))))) (inputs `(("python" ,python-2))) (home-page "https://github.com/dparks1134/ExpressBetaDiversity") (synopsis "Taxon- and phylogenetic-based beta diversity measures") (description "Express Beta Diversity (EBD) calculates ecological beta diversity (dissimilarity) measures between biological communities. EBD implements a variety of diversity measures including those that make use of phylogenetic similarity of community members.") (license license:gpl3+))) (define-public fanc (let ((commit "354401e52ba2320e6b1ba0d3b5aab3541d31c9f3") (revision "1")) (package (name "fanc") (version (git-version "0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/vaquerizaslab/fanc.git") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0vp2cak5snla4j2q23d3ixx016bwzvxfiv4z6yp7anl0xaksd5bl")))) (build-system pyproject-build-system) (arguments (list #:test-flags '(list "-m" "not longrunning" ;; XXX: some of the tests here just take forever "--ignore=fanc/test/test_matrix.py"))) (propagated-inputs (list python-biopython python-cooler python-deprecated python-future python-genomic-regions python-gridmap python-h5py python-imageio python-intervaltree python-matplotlib python-msgpack python-msgpack-numpy python-numpy python-pandas python-pillow python-progressbar2 python-pybedtools python-pybigwig python-pysam python-pywavelets python-pyyaml python-scikit-image python-scikit-learn python-scipy python-seaborn python-tables python-tifffile)) (native-inputs (list python-cython python-pytest)) (home-page "https://github.com/vaquerizaslab/fanc") (synopsis "Framework for the analysis of C-like data") (description "FAN-C provides a pipeline for analysing Hi-C data starting at mapped paired-end sequencing reads.") (license license:gpl3+)))) (define-public fasttree (package (name "fasttree") (version "2.1.10") (source (origin (method url-fetch) (uri (string-append "http://www.microbesonline.org/fasttree/FastTree-" version ".c")) (sha256 (base32 "0vcjdvy1j4m702vmak4svbfkrpcw63k7wymfksjp9a982zy8kjsl")))) (build-system gnu-build-system) (arguments `(#:tests? #f ; no "check" target #:phases (modify-phases %standard-phases (delete 'unpack) (delete 'configure) (replace 'build (lambda* (#:key source #:allow-other-keys) (invoke "gcc" "-O3" "-finline-functions" "-funroll-loops" "-Wall" "-o" "FastTree" source "-lm") (invoke "gcc" "-DOPENMP" "-fopenmp" "-O3" "-finline-functions" "-funroll-loops" "-Wall" "-o" "FastTreeMP" source "-lm") #t)) (replace 'install (lambda* (#:key outputs #:allow-other-keys) (let ((bin (string-append (assoc-ref outputs "out") "/bin"))) (install-file "FastTree" bin) (install-file "FastTreeMP" bin) #t)))))) (home-page "http://www.microbesonline.org/fasttree") (synopsis "Infers approximately-maximum-likelihood phylogenetic trees") (description "FastTree can handle alignments with up to a million of sequences in a reasonable amount of time and memory. For large alignments, FastTree is 100-1,000 times faster than PhyML 3.0 or RAxML 7.") (license license:gpl2+))) (define-public fastx-toolkit (package (name "fastx-toolkit") (version "0.0.14") (source (origin (method url-fetch) (uri (string-append "https://github.com/agordon/fastx_toolkit/releases/download/" version "/fastx_toolkit-" version ".tar.bz2")) (sha256 (base32 "01jqzw386873sr0pjp1wr4rn8fsga2vxs1qfmicvx1pjr72007wy")))) (build-system gnu-build-system) (inputs (list libgtextutils)) (native-inputs (list gcc-6 ;; doesn't build with later versions pkg-config)) (home-page "http://hannonlab.cshl.edu/fastx_toolkit/") (synopsis "Tools for FASTA/FASTQ file preprocessing") (description "The FASTX-Toolkit is a collection of command line tools for Short-Reads FASTA/FASTQ files preprocessing. Next-Generation sequencing machines usually produce FASTA or FASTQ files, containing multiple short-reads sequences. The main processing of such FASTA/FASTQ files is mapping the sequences to reference genomes. However, it is sometimes more productive to preprocess the files before mapping the sequences to the genome---manipulating the sequences to produce better mapping results. The FASTX-Toolkit tools perform some of these preprocessing tasks.") (license license:agpl3+))) (define-public flash (package (name "flash") (version "1.2.11") (source (origin (method url-fetch) (uri (string-append "mirror://sourceforge/flashpage/FLASH-" version ".tar.gz")) (sha256 (base32 "1b1ns9ghbcxy92xwa2a53ikqacvnyhvca0zfv0s7986xzvvscp38")))) (build-system gnu-build-system) (arguments (list #:make-flags #~(list (string-append "CC=" #$(cc-for-target))) #:tests? #f ;no tests #:phases #~(modify-phases %standard-phases ;; No configure script (delete 'configure) ;; No install target (replace 'install (lambda _ (install-file "flash" (string-append #$output "/bin"))))))) (inputs (list zlib)) (home-page "http://ccb.jhu.edu/software/FLASH/") (synopsis "Merge paired-end nucleotide reads from NGS experiments") (description "FLASH (Fast Length Adjustment of SHort reads) is a tool to merge paired-end reads from next-generation sequencing experiments. FLASH is designed to merge pairs of reads when the original DNA fragments are shorter than twice the length of reads. The resulting longer reads can significantly improve genome assemblies. They can also improve transcriptome assembly when FLASH is used to merge RNA-seq data.") (license license:gpl3+))) (define-public flexbar (package (name "flexbar") (version "3.4.0") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/seqan/flexbar") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "1pq9sxvdnldl14libk234m72dqhwgzs3acgl943wchwdqlcsi5r2")))) (build-system cmake-build-system) (arguments `(#:phases (modify-phases %standard-phases (add-after 'unpack 'do-not-tune-to-CPU (lambda _ (substitute* "src/CMakeLists.txt" ((" -march=native") "")))) (replace 'check (lambda* (#:key outputs #:allow-other-keys) (setenv "PATH" (string-append (getcwd) ":" (getenv "PATH"))) (with-directory-excursion "../source/test" (invoke "bash" "flexbar_test.sh")))) (replace 'install (lambda* (#:key outputs #:allow-other-keys) (let* ((out (string-append (assoc-ref outputs "out"))) (bin (string-append out "/bin/"))) (install-file "flexbar" bin))))))) (inputs (list tbb-2020 zlib)) (native-inputs (list pkg-config seqan-2)) (home-page "https://github.com/seqan/flexbar") (synopsis "Barcode and adapter removal tool for sequencing platforms") (description "Flexbar preprocesses high-throughput nucleotide sequencing data efficiently. It demultiplexes barcoded runs and removes adapter sequences. Moreover, trimming and filtering features are provided. Flexbar increases read mapping rates and improves genome and transcriptome assemblies. It supports next-generation sequencing data in fasta/q and csfasta/q format from Illumina, Roche 454, and the SOLiD platform.") (license license:bsd-3))) (define-public fxtract (let ((util-commit "776ca85a18a47492af3794745efcb4a905113115")) (package (name "fxtract") (version "2.3") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/ctSkennerton/fxtract") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "0hab3gpwf4w9s87qlbswq6ws1qqybh4dcqk79q1ahyldzai5fgp5")))) (build-system gnu-build-system) (arguments `(#:make-flags ,#~(list (string-append "PREFIX=" #$output) "CC=gcc") #:test-target "fxtract_test" #:phases (modify-phases %standard-phases (delete 'configure) (add-before 'build 'copy-util (lambda* (#:key inputs #:allow-other-keys) (rmdir "util") (copy-recursively (assoc-ref inputs "ctskennerton-util") "util") #t)) ;; Do not use make install as this requires additional dependencies. (replace 'install (lambda* (#:key outputs #:allow-other-keys) (let* ((out (assoc-ref outputs "out")) (bin (string-append out"/bin"))) (install-file "fxtract" bin) #t)))))) (inputs (list pcre zlib)) (native-inputs ;; ctskennerton-util is licensed under GPL2. `(("ctskennerton-util" ,(origin (method git-fetch) (uri (git-reference (url "https://github.com/ctSkennerton/util") (commit util-commit))) (file-name (string-append "ctstennerton-util-" util-commit "-checkout")) (sha256 (base32 "0cls1hd4vgj3f36fpzzg4xc77d6f3hpc60cbpfmn2gdr7ykzzad7")))))) (home-page "https://github.com/ctSkennerton/fxtract") (synopsis "Extract sequences from FASTA and FASTQ files") (description "Fxtract extracts sequences from a protein or nucleotide fastx (FASTA or FASTQ) file given a subsequence. It uses a simple substring search for basic tasks but can change to using POSIX regular expressions, PCRE, hash lookups or multi-pattern searching as required. By default fxtract looks in the sequence of each record but can also be told to look in the header, comment or quality sections.") ;; 'util' requires SSE instructions. (supported-systems '("x86_64-linux")) (license license:expat)))) (define-public gemma (package (name "gemma") (version "0.98.3") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/genetics-statistics/GEMMA") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "1p8a7kkfn1mmrg017aziy544aha8i9h6wd1x2dk3w2794wl33qb7")) (modules '((guix build utils))) (snippet '(begin (delete-file-recursively "contrib") #t)))) (build-system gnu-build-system) (inputs (list gsl openblas zlib)) (native-inputs `(("catch" ,catch2-1) ("perl" ,perl) ("shunit2" ,shunit2) ("which" ,which))) (arguments `(#:phases (modify-phases %standard-phases (delete 'configure) (add-after 'unpack 'prepare-build (lambda* (#:key inputs #:allow-other-keys) (mkdir-p "bin") (substitute* "Makefile" (("/usr/local/opt/openblas") (assoc-ref inputs "openblas"))) #t)) (replace 'check (lambda* (#:key tests? #:allow-other-keys) (when tests? ;; 'make slow-check' expects shunit2-2.0.3. (with-directory-excursion "test" (invoke "./test_suite.sh")) #t))) (replace 'install (lambda* (#:key outputs #:allow-other-keys) (install-file "bin/gemma" (string-append (assoc-ref outputs "out") "/bin")) #t))))) (home-page "https://github.com/genetics-statistics/GEMMA") (synopsis "Tool for genome-wide efficient mixed model association") (description "@acronym{GEMMA, Genome-wide Efficient Mixed Model Association} provides a standard linear mixed model resolver with application in @acronym{GWAS, genome-wide association studies}.") (license license:gpl3))) (define-public hisat (package (name "hisat") (version "0.1.6") (source (origin (method url-fetch) (uri (string-append "http://ccb.jhu.edu/software/hisat/downloads/hisat-" version "-beta-source.zip")) (sha256 (base32 "177z85vqp9b30vgxl5py5hz4mm37ila37nzhfam23ci9iyfxgyv9")))) (build-system gnu-build-system) (arguments `(#:tests? #f ;no check target #:make-flags '("allall" ;; Disable unsupported `popcnt' instructions on ;; architectures other than x86_64 ,@(if (string-prefix? "x86_64" (or (%current-target-system) (%current-system))) '() '("POPCNT_CAPABILITY=0"))) #:phases (modify-phases %standard-phases (add-after 'unpack 'patch-sources (lambda _ ;; XXX Cannot use snippet because zip files are not supported (substitute* "Makefile" (("^CC = .*$") "CC = gcc") (("^CPP = .*$") "CPP = g++") ;; replace BUILD_HOST and BUILD_TIME for deterministic build (("-DBUILD_HOST=.*") "-DBUILD_HOST=\"\\\"guix\\\"\"") (("-DBUILD_TIME=.*") "-DBUILD_TIME=\"\\\"0\\\"\"")) (substitute* '("hisat-build" "hisat-inspect") (("/usr/bin/env") (which "env"))) ;; This "extended character" is not considered valid. (substitute* "processor_support.h" (("“") "\"") (("”") "\"")))) (replace 'install (lambda* (#:key outputs #:allow-other-keys) (let ((bin (string-append (assoc-ref outputs "out") "/bin/"))) (for-each (lambda (file) (install-file file bin)) (find-files "." "hisat(-(build|align|inspect)(-(s|l)(-debug)*)*)*$"))))) (delete 'configure)))) (native-inputs (list gcc-10 unzip)) (inputs (list perl python zlib)) ;; Non-portable SSE instructions are used so building fails on platforms ;; other than x86_64. (supported-systems '("x86_64-linux")) (home-page "https://ccb.jhu.edu/software/hisat/index.shtml") (synopsis "Hierarchical indexing for spliced alignment of transcripts") (description "HISAT is a fast and sensitive spliced alignment program for mapping RNA-seq reads. In addition to one global FM index that represents a whole genome, HISAT uses a large set of small FM indexes that collectively cover the whole genome. These small indexes (called local indexes) combined with several alignment strategies enable effective alignment of RNA-seq reads, in particular, reads spanning multiple exons.") (license license:gpl3+))) (define-public hisat2 (package (name "hisat2") (version "2.2.1") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/DaehwanKimLab/hisat2/") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "0lmzdhzjkvxw7n5w40pbv5fgzd4cz0f9pxczswn3d4cr0k10k754")))) (build-system gnu-build-system) (arguments `(#:tests? #f ; no check target #:make-flags (list "CC=gcc" "CXX=g++" "allall") #:modules ((guix build gnu-build-system) (guix build utils) (srfi srfi-26)) #:phases (modify-phases %standard-phases (add-after 'unpack 'make-deterministic (lambda _ (substitute* "Makefile" (("`date`") "0")))) (delete 'configure) (add-before 'build 'build-manual (lambda _ (mkdir-p "doc") (invoke "make" "doc"))) (replace 'install (lambda* (#:key outputs #:allow-other-keys) (let* ((out (assoc-ref outputs "out")) (bin (string-append out "/bin/")) (doc (string-append out "/share/doc/hisat2/"))) (for-each (cut install-file <> bin) (find-files "." "hisat2(-(build|align|inspect)(-(s|l)(-debug)*)*)*$")) (mkdir-p doc) (install-file "doc/manual.inc.html" doc))))))) (native-inputs (list perl pandoc)) ; for documentation (inputs `(("python" ,python-wrapper))) (home-page "https://daehwankimlab.github.io/hisat2/") (synopsis "Graph-based alignment of genomic sequencing reads") (description "HISAT2 is a fast and sensitive alignment program for mapping next-generation sequencing reads (both DNA and RNA) to a population of human genomes (as well as to a single reference genome). In addition to using one global @dfn{graph FM} (GFM) index that represents a population of human genomes, HISAT2 uses a large set of small GFM indexes that collectively cover the whole genome. These small indexes, combined with several alignment strategies, enable rapid and accurate alignment of sequencing reads. This new indexing scheme is called a @dfn{Hierarchical Graph FM index} (HGFM).") ;; HISAT2 contains files from Bowtie2, which is released under ;; GPLv2 or later. The HISAT2 source files are released under ;; GPLv3 or later. (license license:gpl3+))) (define-public homer (package (name "homer") (version "4.11.1") (source (origin (method url-fetch/zipbomb) (uri (string-append "http://homer.ucsd.edu/homer/data/software/homer.v" version ".zip")) (sha256 (base32 "0ay802swzq6ix9d8fkinpplcvyc1xyi3cjmj2x08jab7c40cvlc0")))) (build-system gnu-build-system) (arguments (list #:phases #~(modify-phases %standard-phases (replace 'configure (lambda _ (let ((share (string-append #$output "/share/homer"))) (mkdir-p share) (substitute* "configureHomer.pl" (("my \\$homeDir = \\$1;") (string-append "my $homeDir = \"" share "\";")))))) (replace 'build (lambda _ (let ((share (string-append #$output "/share/homer"))) (copy-recursively "." share)) (invoke "perl" "configureHomer.pl" "-local"))) (replace 'check (lambda* (#:key tests? #:allow-other-keys) (when tests? (invoke (string-append #$output "/share/homer/bin/homer2"))))) (replace 'install (lambda _ (mkdir-p (string-append #$output "/bin")) (symlink (string-append #$output "/share/homer/bin/homer2") (string-append #$output "/bin/homer2")) (for-each patch-shebang (find-files (string-append #$output "/share/homer/bin") "\\.pl$"))))))) (inputs (list perl)) (native-inputs (list perl unzip)) (home-page "http://homer.ucsd.edu/homer") (synopsis "Motif discovery and next generation sequencing analysis") (description "HOMER (Hypergeometric Optimization of Motif EnRichment) is a suite of tools for Motif Discovery and next-gen sequencing analysis. It is a collection of command line programs written in Perl and C++. HOMER was primarily written as a de novo motif discovery algorithm and is well suited for finding 8-20 bp motifs in large scale genomics data. HOMER contains many useful tools for analyzing ChIP-Seq, GRO-Seq, RNA-Seq, DNase-Seq, Hi-C and numerous other types of functional genomics sequencing data sets.") (license license:gpl3+))) (define-public hmmer (package (name "hmmer") (version "3.3.2") (source (origin (method url-fetch) (uri (string-append "http://eddylab.org/software/hmmer/hmmer-" version ".tar.gz")) (sha256 (base32 "0s9wf6n0qanbx8qs6igfl3vyjikwbrvh4d9d6mv54yp3xysykzlj")))) (build-system gnu-build-system) (native-inputs (list perl python)) ; for tests (home-page "http://hmmer.org/") (synopsis "Biosequence analysis using profile hidden Markov models") (description "HMMER is used for searching sequence databases for homologs of protein sequences, and for making protein sequence alignments. It implements methods using probabilistic models called profile hidden Markov models (profile HMMs).") ;; hmmer uses non-portable SSE intrinsics so building fails on other ;; platforms. (supported-systems '("x86_64-linux" "i686-linux")) (license license:bsd-3))) (define-public htseq (package (name "htseq") (version "2.0.2") ;; Sources on pypi do not include everything needed to run the tests. (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/htseq/htseq") (commit (string-append "release_" version)))) (file-name (git-file-name name version)) (sha256 (base32 "1kbr4ydjjhizz6r5m3xd4f0wj7qnn8zs0vnzghhgaa0yhbya5r19")))) (build-system python-build-system) (arguments (list #:phases '(modify-phases %standard-phases ;; Avoid rebuilding the extension. Everything is built during the ;; 'install phase anyway. (delete 'build) (replace 'check (lambda* (#:key tests? #:allow-other-keys) (when tests? (invoke "pytest" "-v"))))))) (propagated-inputs (list python-matplotlib python-numpy python-pysam)) (native-inputs (list python-cython python-pandas python-pytest python-scipy swig)) (home-page "https://github.com/htseq") (synopsis "Framework for analyzing high-throughput sequencing data") (description "This package provides a framework to process and analyze data from high-throughput sequencing (HTS) assays") (license license:gpl3+))) (define-public python-genomepy (package (name "python-genomepy") (version "0.15.0") (source (origin (method url-fetch) (uri (pypi-uri "genomepy" version)) (sha256 (base32 "0jmyvnsn6w0djjmxh4fjspy1346337jzihxb276v3s275r6zjmln")))) (build-system pyproject-build-system) (arguments (list ;; The tests require internet access. #:tests? #false #:phases '(modify-phases %standard-phases ;; Needed by tests (add-after 'unpack 'set-HOME (lambda _ (setenv "HOME" "/tmp")))))) (propagated-inputs (list python-appdirs python-biopython python-click python-colorama python-diskcache ;; We cannot use an older filelock, because the ;; @lock annotation is used here. python-filelock-3.5 python-loguru python-mygene python-mysql-connector-python python-norns python-numpy python-pandas python-pyfaidx python-requests python-tqdm)) (native-inputs (list python-hatchling python-pytest)) (home-page "https://vanheeringen-lab.github.io/genomepy/") (synopsis "Genes and genomes at your fingertips") (description "genomepy is designed to provide a simple and straightforward way to download and use genomic data. This includes @enumerate @item searching available data, @item showing the available metadata, @item automatically downloading, preprocessing and matching data, and @item generating optional aligner indexes. @end enumerate All with sensible, yet controllable defaults.") (license license:expat))) (define-public java-htsjdk (package (name "java-htsjdk") (version "2.3.0") ; last version without build dependency on gradle (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/samtools/htsjdk") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "1b178ixcabanm834ydjl3jiakpyxdmki32hqfv2abrzn3rcwa28i")) (modules '((guix build utils))) (snippet ;; Delete pre-built binaries '(begin (delete-file-recursively "lib") (mkdir-p "lib") #t)))) (build-system ant-build-system) (arguments `(#:tests? #f ; test require Internet access #:jdk ,icedtea-8 #:make-flags ,#~(list (string-append "-Ddist=" #$output "/share/java/htsjdk/")) #:build-target "all" #:phases (modify-phases %standard-phases ;; The build phase also installs the jars (delete 'install)))) (inputs `(("java-ngs" ,java-ngs) ("java-snappy-1" ,java-snappy-1) ("java-commons-compress" ,java-commons-compress) ("java-commons-logging-minimal" ,java-commons-logging-minimal) ("java-commons-jexl-2" ,java-commons-jexl-2) ("java-xz" ,java-xz))) (native-inputs (list java-testng)) (home-page "https://samtools.github.io/htsjdk/") (synopsis "Java API for high-throughput sequencing data (HTS) formats") (description "HTSJDK is an implementation of a unified Java library for accessing common file formats, such as SAM and VCF, used for high-throughput sequencing (HTS) data. There are also an number of useful utilities for manipulating HTS data.") (license license:expat))) (define-public java-htsjdk-latest (package (name "java-htsjdk") (version "2.14.3") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/samtools/htsjdk") (commit version))) (file-name (string-append name "-" version "-checkout")) (sha256 (base32 "1lmya1fdjy03mz6zmdmd86j9v9vfhqb3952mqq075navx1i6g4bc")))) (build-system ant-build-system) (arguments `(#:tests? #f ; test require Scala #:jdk ,icedtea-8 #:jar-name "htsjdk.jar" #:phases (modify-phases %standard-phases (add-after 'unpack 'remove-useless-build.xml (lambda _ (delete-file "build.xml") #t)) ;; The tests require the scalatest package. (add-after 'unpack 'remove-tests (lambda _ (delete-file-recursively "src/test") #t))))) (inputs `(("java-ngs" ,java-ngs) ("java-snappy-1" ,java-snappy-1) ("java-commons-compress" ,java-commons-compress) ("java-commons-logging-minimal" ,java-commons-logging-minimal) ("java-commons-jexl-2" ,java-commons-jexl-2) ("java-xz" ,java-xz))) (native-inputs (list java-junit)) (home-page "https://samtools.github.io/htsjdk/") (synopsis "Java API for high-throughput sequencing data (HTS) formats") (description "HTSJDK is an implementation of a unified Java library for accessing common file formats, such as SAM and VCF, used for high-throughput sequencing (HTS) data. There are also an number of useful utilities for manipulating HTS data.") (license license:expat))) ;; This is needed for picard 2.10.3 (define-public java-htsjdk-2.10.1 (package (inherit java-htsjdk-latest) (name "java-htsjdk") (version "2.10.1") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/samtools/htsjdk") (commit version))) (file-name (string-append name "-" version "-checkout")) (sha256 (base32 "1kxh7slm2pm3x9p6jxa1wqsq9a31dhiiflhxnxqcisan4k3rwia2")))) (build-system ant-build-system) (arguments `(#:tests? #f ; tests require Scala #:jdk ,icedtea-8 #:jar-name "htsjdk.jar" #:phases (modify-phases %standard-phases (add-after 'unpack 'remove-useless-build.xml (lambda _ (delete-file "build.xml") #t)) ;; The tests require the scalatest package. (add-after 'unpack 'remove-tests (lambda _ (delete-file-recursively "src/test") #t))))))) (define-public java-maxent (package (name "java-maxent") (version "3.4.4") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/mrmaxent/Maxent") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "12q7hhly76l77vm8w8v9icga2gn6xs0bw33a7wb7zikcmvizcyp0")))) (build-system ant-build-system) (arguments (list #:tests? #false ;there are none #:jdk icedtea-8 #:phases #~(modify-phases %standard-phases (replace 'build (lambda* (#:key inputs #:allow-other-keys) ;; See https://github.com/mrmaxent/Maxent/pull/11 (substitute* "density/Extractor.java" (("float") "double")) (with-directory-excursion "gnu/getopt/" (invoke "make")) (mkdir-p "ptii") (with-directory-excursion "ptii" (invoke "tar" "xvf" (assoc-ref inputs "ptii") "--strip-components=1") (copy-recursively "com" "../com")) (delete-file-recursively "ptii") (apply invoke "javac" "-cp" (getcwd) "-g" (find-files "com/microstar/xml" "\\.java$")) (apply invoke "javac" "-cp" (getcwd) "-g" (find-files "density" "\\.java$")) ;; This needs the proprietary com.sun.image.codec.jpeg module. (delete-file "ptolemy/plot/servlet/PlotServlet.java") (apply invoke "javac" "-cp" (string-append (getcwd) ":" (getenv "CLASSPATH")) "-g" (find-files "ptolemy/plot" "\\.java$")) (apply invoke "javac" "-cp" (getcwd) "-g" (find-files "com" "\\.java$")) (apply invoke "javac" "-cp" (getcwd) "-g" (find-files "gui" "\\.java$")) (apply invoke "jar" "cvfm" "maxent.jar" (cons* "density/mc.mf" "density/parameters.csv" (append (find-files "density" "\\.class$") (find-files "density" "\\.html$") (find-files "gnu/getopt" ".*") (find-files "gui/layouts" "\\.class$") (find-files "com/macfaq/io" "\\.class$") (find-files "density/tools" "\\.class$") (find-files "ptolemy/plot" "\\.class$")))))) (replace 'install (lambda _ (install-file "maxent.jar" (string-append #$output "/share/java/maxent/"))))))) (inputs (list java-classpathx-servletapi)) (native-inputs `(("make" ,gnu-make) ;; For com.microstar.xml ("ptii" ,(let ((version "4.0.1")) (origin (method url-fetch) (uri (string-append "https://ptolemy.berkeley.edu/ptolemyII/ptII" (version-major+minor version) "/ptII" version ".src.tar.gz")) (sha256 (base32 "0ifmmvrcipcnd4b9im1g379ffrs7g7k99sw5vv9d9h3hzq6hqv21"))))))) (home-page "http://biodiversityinformatics.amnh.org/open_source/maxent") (synopsis "Model species geographic distributions") (description "Maxent is a stand-alone Java application for modelling species geographic distributions.") (license license:expat))) ;; This version matches java-htsjdk 2.3.0. Later versions also require a more ;; recent version of java-htsjdk, which depends on gradle. (define-public java-picard (package (name "java-picard") (version "2.3.0") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/broadinstitute/picard") (commit version))) (file-name (string-append "java-picard-" version "-checkout")) (sha256 (base32 "1ll7mf4r3by92w2nhlmpa591xd1f46xlkwh59mq6fvbb5pdwzvx6")) (modules '((guix build utils))) (snippet '(begin ;; Delete pre-built binaries. (delete-file-recursively "lib") (mkdir-p "lib") (substitute* "build.xml" ;; Remove build-time dependency on git. (("failifexecutionfails=\"true\"") "failifexecutionfails=\"false\"") ;; Use our htsjdk. (("depends=\"compile-htsjdk, ") "depends=\"") (("depends=\"compile-htsjdk-tests, ") "depends=\"") ;; Build picard-lib.jar before building picard.jar (("name=\"picard-jar\" depends=\"" line) (string-append line "picard-lib-jar, "))) #t)))) (build-system ant-build-system) (arguments `(#:build-target "picard-jar" #:test-target "test" ;; Tests require jacoco:coverage. #:tests? #f #:make-flags ,#~(list (string-append "-Dhtsjdk_lib_dir=" #$(this-package-input "java-htsjdk") "/share/java/htsjdk/") "-Dhtsjdk-classes=dist/tmp" (string-append "-Dhtsjdk-version=" #$(package-version java-htsjdk))) #:jdk ,icedtea-8 #:phases (modify-phases %standard-phases ;; FIXME: this phase fails with "duplicate entry: htsjdk/samtools/AbstractBAMFileIndex$1.class" (delete 'generate-jar-indices) (add-after 'unpack 'fix-guava (lambda _ (substitute* "src/java/picard/cmdline/CommandLineParser.java" (("CharMatcher.ASCII") "CharMatcher.ascii()")))) (add-after 'unpack 'use-our-htsjdk (lambda* (#:key inputs #:allow-other-keys) (substitute* "build.xml" (("\\$\\{htsjdk\\}/lib") (search-input-directory inputs "share/java/htsjdk"))))) (add-after 'unpack 'make-test-target-independent (lambda* (#:key inputs #:allow-other-keys) (substitute* "build.xml" (("name=\"test\" depends=\"compile, ") "name=\"test\" depends=\"")) #t)) (replace 'install (install-jars "dist"))))) (inputs (list java-htsjdk java-guava)) (native-inputs (list java-testng)) (home-page "https://broadinstitute.github.io/picard/") (synopsis "Tools for manipulating high-throughput sequencing data and formats") (description "Picard is a set of Java command line tools for manipulating high-throughput sequencing (HTS) data and formats. Picard is implemented using the HTSJDK Java library to support accessing file formats that are commonly used for high-throughput sequencing data such as SAM, BAM, CRAM and VCF.") (license license:expat))) ;; This is needed for dropseq-tools (define-public java-picard-2.10.3 (package (name "java-picard") (version "2.10.3") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/broadinstitute/picard") (commit version))) (file-name (string-append "java-picard-" version "-checkout")) (sha256 (base32 "1ajlx31l6i1k3y2rhnmgq07sz99g2czqfqgkr9mihmdjp3gwjhvi")))) (build-system ant-build-system) (arguments `(#:jar-name "picard.jar" ;; Tests require jacoco:coverage. #:tests? #f #:jdk ,icedtea-8 #:main-class "picard.cmdline.PicardCommandLine" #:modules ((guix build ant-build-system) (guix build utils) (guix build java-utils) (sxml simple) (sxml transform) (sxml xpath)) #:phases (modify-phases %standard-phases ;; FIXME: this phase fails with "duplicate entry: htsjdk/samtools/AbstractBAMFileIndex$1.class" (delete 'generate-jar-indices) (add-after 'unpack 'remove-useless-build.xml (lambda _ (delete-file "build.xml") #t)) (add-after 'unpack 'fix-guava (lambda _ (substitute* "src/main/java/picard/cmdline/CommandLineParser.java" (("CharMatcher.ASCII") "CharMatcher.ascii()")))) ;; This is necessary to ensure that htsjdk is found when using ;; picard.jar as an executable. (add-before 'build 'edit-classpath-in-manifest (lambda* (#:key inputs #:allow-other-keys) (chmod "build.xml" #o664) (call-with-output-file "build.xml.new" (lambda (port) (sxml->xml (pre-post-order (with-input-from-file "build.xml" (lambda _ (xml->sxml #:trim-whitespace? #t))) `((target . ,(lambda (tag . kids) (let ((name ((sxpath '(name *text*)) (car kids))) ;; FIXME: We're breaking the line ;; early with a dummy path to ;; ensure that the store reference ;; isn't broken apart and can still ;; be found by the reference ;; scanner. (msg (format #f "\ Class-Path: /~a \ ~a/share/java/htsjdk.jar${line.separator}${line.separator}" ;; maximum line length is 70 (string-tabulate (const #\b) 57) (assoc-ref inputs "java-htsjdk")))) (if (member "manifest" name) `(,tag ,@kids (replaceregexp (@ (file "${manifest.file}") (match "\\r\\n\\r\\n") (replace "${line.separator}"))) (echo (@ (message ,msg) (file "${manifest.file}") (append "true")))) `(,tag ,@kids))))) (*default* . ,(lambda (tag . kids) `(,tag ,@kids))) (*text* . ,(lambda (_ txt) txt)))) port))) (rename-file "build.xml.new" "build.xml") #t))))) (propagated-inputs (list java-htsjdk-2.10.1)) (native-inputs (list java-testng java-guava)) (home-page "https://broadinstitute.github.io/picard/") (synopsis "Tools for manipulating high-throughput sequencing data and formats") (description "Picard is a set of Java command line tools for manipulating high-throughput sequencing (HTS) data and formats. Picard is implemented using the HTSJDK Java library to support accessing file formats that are commonly used for high-throughput sequencing data such as SAM, BAM, CRAM and VCF.") (license license:expat))) ;; This is the last version of Picard to provide net.sf.samtools (define-public java-picard-1.113 (package (inherit java-picard) (name "java-picard") (version "1.113") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/broadinstitute/picard") (commit version))) (file-name (string-append "java-picard-" version "-checkout")) (sha256 (base32 "0lkpvin2fz3hhly4l02kk56fqy8lmlgyzr9kmvljk6ry6l1hw973")) (modules '((guix build utils))) (snippet '(begin ;; Delete pre-built binaries. (delete-file-recursively "lib") (mkdir-p "lib"))))) (build-system ant-build-system) (arguments `(#:build-target "picard-jar" #:test-target "test" ;; FIXME: the class path at test time is wrong. ;; [testng] Error: A JNI error has occurred, please check your installation and try again ;; [testng] Exception in thread "main" java.lang.NoClassDefFoundError: com/beust/jcommander/ParameterException #:tests? #f #:jdk ,icedtea-8 #:ant ,ant/java8 ;; This is only used for tests. #:make-flags (list "-Dsamjdk.intel_deflater_so_path=lib/jni/libIntelDeflater.so") #:phases (modify-phases %standard-phases ;; FIXME: This phase fails. (delete 'generate-jar-indices) ;; Do not use bundled ant bzip2. (add-after 'unpack 'use-ant-bzip (lambda* (#:key inputs #:allow-other-keys) (substitute* "build.xml" (("\\$\\{lib\\}/apache-ant-1.8.2-bzip2.jar") (search-input-file inputs "/lib/ant.jar"))))) (add-after 'unpack 'make-test-target-independent (lambda* (#:key inputs #:allow-other-keys) (substitute* "build.xml" (("name=\"test\" depends=\"compile, ") "name=\"test\" depends=\"compile-tests, ") (("name=\"compile\" depends=\"compile-src, compile-tests\"") "name=\"compile\" depends=\"compile-src\"")))) (add-after 'unpack 'fix-deflater-path (lambda* (#:key outputs #:allow-other-keys) (substitute* "src/java/net/sf/samtools/Defaults.java" (("getStringProperty\$\"intel_deflater_so_path\", null\$") (string-append "getStringProperty(\"intel_deflater_so_path\", \"" (assoc-ref outputs "out") "/lib/jni/libIntelDeflater.so" "\")"))))) ;; Build the deflater library, because we've previously deleted the ;; pre-built one. This can only be built with access to the JDK ;; sources. (add-after 'build 'build-jni (lambda* (#:key inputs #:allow-other-keys) (mkdir-p "lib/jni") (mkdir-p "jdk-src") (invoke "tar" "--strip-components=1" "-C" "jdk-src" "-xf" (assoc-ref inputs "jdk-src")) (invoke "javah" "-jni" "-classpath" "classes" "-d" "lib/" "net.sf.samtools.util.zip.IntelDeflater") (with-directory-excursion "src/c/inteldeflater" (invoke "gcc" "-I../../../lib" "-I." (string-append "-I" (assoc-ref inputs "jdk") "/include/linux") "-I../../../jdk-src/src/share/native/common/" "-I../../../jdk-src/src/solaris/native/common/" "-c" "-O3" "-fPIC" "IntelDeflater.c") (invoke "gcc" "-shared" "-o" "../../../lib/jni/libIntelDeflater.so" "IntelDeflater.o" "-lz" "-lstdc++")))) ;; We can only build everything else after building the JNI library. (add-after 'build-jni 'build-rest (lambda* (#:key make-flags #:allow-other-keys) (apply invoke `("ant" "all" ,@make-flags)))) (add-before 'build 'set-JAVA6_HOME (lambda _ (setenv "JAVA6_HOME" (getenv "JAVA_HOME")))) (replace 'install (install-jars "dist")) (add-after 'install 'install-jni-lib (lambda* (#:key outputs #:allow-other-keys) (let ((jni (string-append (assoc-ref outputs "out") "/lib/jni"))) (mkdir-p jni) (install-file "lib/jni/libIntelDeflater.so" jni))))))) (inputs (list java-snappy-1 java-commons-jexl-2 java-cofoja ant/java8 ;for bzip2 support at runtime zlib)) (native-inputs `(("ant-apache-bcel" ,ant-apache-bcel) ("ant-junit" ,ant-junit) ("java-testng" ,java-testng) ("java-commons-bcel" ,java-commons-bcel) ("java-jcommander" ,java-jcommander) ("jdk" ,icedtea-8 "jdk") ("jdk-src" ,(car (assoc-ref (package-native-inputs icedtea-8) "jdk-drop"))))))) (define-public fastqc (package (name "fastqc") (version "0.11.9") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/s-andrews/FastQC") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "00y9drm0bkpxw8xfl8ysss18jmnhj8blgqgr6fpa58rkpfcbg8qk")) (snippet '(for-each delete-file '("cisd-jhdf5.jar" "sam-1.103.jar" "jbzip2-0.9.jar"))))) (build-system ant-build-system) (arguments (list #:tests? #f ;there are no tests #:build-target "build" #:phases #~(modify-phases %standard-phases (add-after 'unpack 'fix-dependencies (lambda* (#:key inputs #:allow-other-keys) (substitute* '("build.xml" ".classpath") (("jbzip2-0.9.jar") (search-input-file inputs "/share/java/jbzip2.jar")) (("sam-1.103.jar") (search-input-file inputs "/share/java/sam-1.112.jar")) (("cisd-jhdf5.jar") (search-input-file inputs "/share/java/sis-jhdf5.jar"))))) ;; There is no installation target (replace 'install (lambda* (#:key inputs #:allow-other-keys) (let* ((bin (string-append #$output "/bin")) (share (string-append #$output "/share/fastqc/")) (exe (string-append share "/fastqc"))) (for-each mkdir-p (list bin share)) (copy-recursively "bin" share) (substitute* exe (("my \\$java_bin = \"java\";") (string-append "my $java_bin = \"" ;; Use java from the JRE, not the JDK #$(this-package-input "icedtea") "/bin/java" "\";")) (("\\$RealBin\\$delimiter\\$RealBin.*") (string-append (string-join (list share (search-input-file inputs "/share/java/sam-1.112.jar") (search-input-file inputs "/share/java/jbzip2.jar") (search-input-file inputs "/share/java/sis-jhdf5.jar")) "$delimiter") "\";\n"))) (chmod exe #o555) (symlink exe (string-append bin "/fastqc")))))))) (inputs (list icedtea java-cisd-jhdf5 java-picard-1.113 java-jbzip2 perl)) ;needed for the wrapper script (native-inputs (list unzip)) (home-page "https://www.bioinformatics.babraham.ac.uk/projects/fastqc/") (synopsis "Quality control tool for high throughput sequence data") (description "FastQC aims to provide a simple way to do some quality control checks on raw sequence data coming from high throughput sequencing pipelines. It provides a modular set of analyses which you can use to give a quick impression of whether your data has any problems of which you should be aware before doing any further analysis. The main functions of FastQC are: @itemize @item Import of data from BAM, SAM or FastQ files (any variant); @item Providing a quick overview to tell you in which areas there may be problems; @item Summary graphs and tables to quickly assess your data; @item Export of results to an HTML based permanent report; @item Offline operation to allow automated generation of reports without running the interactive application. @end itemize\n") (license license:gpl3+))) (define-public fastp (package (name "fastp") (version "0.23.2") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/OpenGene/fastp") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "04nmrqpjc3qni0cbazlwvpg8rk1mkfmfma0n4q3zivs3zi6rfnav")))) (build-system gnu-build-system) (arguments (list #:tests? #false ;there are none #:make-flags #~(list (string-append "PREFIX=" #$output)) #:phases #~(modify-phases %standard-phases (delete 'configure) (add-before 'install 'create-target-dir (lambda _ (mkdir-p (string-append #$output "/bin"))))))) (inputs (list isa-l libdeflate)) (home-page "https://github.com/OpenGene/fastp/") (synopsis "All-in-one FastQ preprocessor") (description "Fastp is a tool designed to provide fast all-in-one preprocessing for FastQ files. This tool has multi-threading support to afford high performance.") (license license:expat))) (define-public htscodecs (package (name "htscodecs") (version "1.6.0") (source (origin (method url-fetch) (uri (string-append "https://github.com/samtools/htscodecs/" "releases/download/v" version "/htscodecs-" version ".tar.gz")) (sha256 (base32 "1h0827g9svil9jnjbpdlxjbl44rai5b95m61hs9ifbqrz9nvnjjb")))) (build-system gnu-build-system) (inputs (list bzip2 zlib)) (home-page "https://github.com/samtools/htscodecs") (synopsis "Custom compression for CRAM and others") (description "This package implements the custom CRAM codecs used for \"EXTERNAL\" block types. These consist of two variants of the rANS codec (8-bit and 16-bit renormalisation, with run-length encoding and bit-packing also supported in the latter), a dynamic arithmetic coder, and custom codecs for name/ID compression and quality score compression derived from fqzcomp.") (license (list license:public-domain ;c_range_coder.h, rANS_byte.h, and rANS_word.h license:bsd-3)))) ;all the rest (define-public htslib (package (name "htslib") (version "1.19") (source (origin (method url-fetch) (uri (string-append "https://github.com/samtools/htslib/releases/download/" version "/htslib-" version ".tar.bz2")) (sha256 (base32 "0dh79lwpspwwfbkmllrrhbk8nkvlfc5b5ib4d0xg5ld79w6c8lc7")) (snippet #~(begin (use-modules (guix build utils)) (delete-file-recursively "htscodecs"))))) (build-system gnu-build-system) ;; Let htslib translate "gs://" and "s3://" to regular https links with ;; "--enable-gcs" and "--enable-s3". For these options to work, we also ;; need to set "--enable-libcurl". (arguments `(#:configure-flags '("--enable-gcs" "--enable-libcurl" "--enable-s3" "--with-external-htscodecs"))) (inputs (list bzip2 curl openssl xz)) ;; This is referred to in the pkg-config file as a required library. (propagated-inputs (list htscodecs zlib)) (native-inputs (list perl)) (home-page "https://www.htslib.org") (synopsis "C library for reading/writing high-throughput sequencing data") (description "HTSlib is a C library for reading/writing high-throughput sequencing data. It also provides the @command{bgzip}, @command{htsfile}, and @command{tabix} utilities.") ;; Files under cram/ are released under the modified BSD license; ;; the rest is released under the Expat license (license (list license:expat license:bsd-3)))) (define-public htslib-1.14 (package/inherit htslib (version "1.14") (source (origin (method url-fetch) (uri (string-append "https://github.com/samtools/htslib/releases/download/" version "/htslib-" version ".tar.bz2")) (sha256 (base32 "0pwk8yhhvb85mi1d2qhwsb4samc3rmbcrq7b1s0jz0glaa7in8pd")))) (arguments (substitute-keyword-arguments (package-arguments htslib) ((#:configure-flags cf #~'()) #~(delete "--with-external-htscodecs" #$cf)))) (propagated-inputs (modify-inputs (package-propagated-inputs htslib) (delete "htscodecs"))))) (define-public htslib-1.12 (package/inherit htslib (version "1.12") (source (origin (method url-fetch) (uri (string-append "https://github.com/samtools/htslib/releases/download/" version "/htslib-" version ".tar.bz2")) (sha256 (base32 "1jplnvizgr0fyyvvmkfmnsywrrpqhid3760vw15bllz98qdi9012")))) (arguments (substitute-keyword-arguments (package-arguments htslib) ((#:configure-flags cf #~'()) #~(delete "--with-external-htscodecs" #$cf)))) (propagated-inputs (modify-inputs (package-propagated-inputs htslib) (delete "htscodecs"))))) (define-public htslib-1.10 (package/inherit htslib (version "1.10") (source (origin (method url-fetch) (uri (string-append "https://github.com/samtools/htslib/releases/download/" version "/htslib-" version ".tar.bz2")) (sha256 (base32 "0wm9ay7qgypj3mwx9zl1mrpnr36298b1aj5vx69l4k7bzbclvr3s")))))) (define-public htslib-1.9 (package/inherit htslib (version "1.9") (source (origin (method url-fetch) (uri (string-append "https://github.com/samtools/htslib/releases/download/" version "/htslib-" version ".tar.bz2")) (sha256 (base32 "16ljv43sc3fxmv63w7b2ff8m1s7h89xhazwmbm1bicz8axq8fjz0")))))) ;; This package should be removed once no packages rely upon it. (define htslib-1.3 (package/inherit htslib (version "1.3.1") (source (origin (method url-fetch) (uri (string-append "https://github.com/samtools/htslib/releases/download/" version "/htslib-" version ".tar.bz2")) (sha256 (base32 "1rja282fwdc25ql6izkhdyh8ppw8x2fs0w0js78zgkmqjlikmma9")))))) (define htslib-for-samtools-1.2 (package/inherit htslib (version "1.2.1") (source (origin (method url-fetch) (uri (string-append "https://github.com/samtools/htslib/releases/download/" version "/htslib-" version ".tar.bz2")) (sha256 (base32 "1c32ssscbnjwfw3dra140fq7riarp2x990qxybh34nr1p5r17nxx")))) (arguments `(#:phases (modify-phases %standard-phases (add-after 'unpack 'patch-tests (lambda _ (substitute* "test/test.pl" (("/bin/bash") (which "bash")))))))) (inputs `(("zlib" ,zlib))) (native-inputs `(("perl" ,perl))))) (define htslib-for-stringtie (package (inherit htslib-1.12) (source (origin (inherit (package-source htslib-1.12)) (patches (search-patches "htslib-for-stringtie.patch")))) (arguments `(#:configure-flags '("--with-libdeflate"))) (inputs (list bzip2 libdeflate openssl)))) (define-public idr (package (name "idr") (version "2.0.3") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/nboley/idr") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "04j876h6z444v2q79drxx283d3k5snd72kj895wbalnl42206x9g")) ;; Delete generated C code. (snippet '(begin (delete-file "idr/inv_cdf.c") #t)))) (build-system python-build-system) ;; There is only one test ("test_inv_cdf.py") and it tests features that ;; are no longer part of this package. It also asserts False, which ;; causes the tests to always fail. (arguments `(#:tests? #f)) (propagated-inputs (list python-scipy python-sympy python-numpy python-matplotlib)) (native-inputs (list python-cython)) (home-page "https://github.com/nboley/idr") (synopsis "Tool to measure the irreproducible discovery rate (IDR)") (description "The IDR (Irreproducible Discovery Rate) framework is a unified approach to measure the reproducibility of findings identified from replicate experiments and provide highly stable thresholds based on reproducibility.") (license license:gpl2+))) (define-public isolator (let ((commit "24bafc0a102dce213bfc2b5b9744136ceadaba03") (revision "1")) (package (name "isolator") (version (git-version "0.0.2" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/dcjones/isolator.git") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "12mbcfqhiggcjvzizf2ff7b05z31i47njcyzcivpw5j74pfbr3dv")))) (build-system cmake-build-system) (arguments (list #:tests? #f ;no check target #:phases '(modify-phases %standard-phases (add-after 'unpack 'fix-std (lambda _ (substitute* '("src/summarize.cpp" "src/shredder.cpp") (("isnan") "std::isnan") (("isinf") "std::isinf"))))))) (inputs (list boost hdf5 zlib)) (home-page "https://github.com/dcjones/isolator") (synopsis "Tools for the analysis of RNA-Seq experiments") (description "Isolator analyzes RNA-Seq experiments. Isolator has a particular focus on producing stable, consistent estimates. It implements a full hierarchical Bayesian model of an entire RNA-Seq experiment. It saves all the samples generated by the sampler, which can be processed to compute posterior probabilities for arbitrarily complex questions, far beyond the confines of pairwise tests. It aggressively corrects for technical effects, such as random priming bias, GC-bias, 3' bias, and fragmentation effects. Compared to other MCMC approaches, it is exceedingly efficient, though generally slower than modern maximum likelihood approaches.") (license license:expat)))) (define-public jellyfish (package (name "jellyfish") (version "2.3.0") (source (origin (method url-fetch) (uri (string-append "https://github.com/gmarcais/Jellyfish/" "releases/download/v" version "/jellyfish-" version ".tar.gz")) (sha256 (base32 "0npa62wzasdibas5zp3n8j3armsci4kyvh0jw7jr0am4gg7vg5g1")))) (build-system gnu-build-system) (outputs '("out" ;for library "python")) ;for Python bindings (arguments (list #:configure-flags #~(list "--without-sse" ; configure script probes for CPU features when SSE is enabled. (string-append "--enable-python-binding=" #$output:python)) #:phases '(modify-phases %standard-phases (add-before 'check 'set-SHELL-variable (lambda _ ;; generator_manager.hpp either uses /bin/sh or $SHELL ;; to run tests. (setenv "SHELL" (which "bash"))))))) (native-inputs (list bc time python-wrapper pkg-config)) (inputs (list htslib)) (synopsis "Tool for fast counting of k-mers in DNA") (description "Jellyfish is a tool for fast, memory-efficient counting of k-mers in DNA. A k-mer is a substring of length k, and counting the occurrences of all such substrings is a central step in many analyses of DNA sequence. Jellyfish is a command-line program that reads FASTA and multi-FASTA files containing DNA sequences. It outputs its k-mer counts in a binary format, which can be translated into a human-readable text format using the @code{jellyfish dump} command, or queried for specific k-mers with @code{jellyfish query}.") (home-page "http://www.genome.umd.edu/jellyfish.html") ;; JELLYFISH seems to be 64-bit only. (supported-systems %64bit-supported-systems) ;; One of these licenses may be picked (license (list license:gpl3+ license:bsd-3)))) (define-public khmer (package (name "khmer") (version "3.0.0a3") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/dib-lab/khmer") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "01l4jczglkl7yfhgvzx8j0df7k54bk1r8sli9ll16i1mis0d8f37")) (modules '((guix build utils))) (snippet '(begin ;; Delete bundled libraries. We do not replace the bundled seqan ;; as it is a modified subset of the old version 1.4.1. ;; ;; We do not replace the bundled MurmurHash as the canonical ;; repository for this code 'SMHasher' is unsuitable for providing ;; a library. See ;; https://lists.gnu.org/archive/html/guix-devel/2016-06/msg00977.html (delete-file-recursively "third-party/zlib") (delete-file-recursively "third-party/bzip2") (delete-file-recursively "third-party/seqan") (substitute* "setup.cfg" (("# libraries = z,bz2") "libraries = z,bz2") (("include:third-party/zlib:third-party/bzip2") "include:")) ;; Delete generated Cython CPP files. (for-each delete-file (find-files "khmer/_oxli/" "\\.cpp$")))))) (build-system python-build-system) (arguments `(#:phases (modify-phases %standard-phases (add-after 'unpack 'set-cc (lambda _ (setenv "CC" "gcc"))) (add-after 'unpack 'python-3.8-compatibility (lambda _ ;; Python 3.8 removed time.clock(). (substitute* "sandbox/sweep-reads.py" (("time\\.clock") "time.process_time")))) (add-after 'unpack 'do-use-cython (lambda _ (substitute* "setup.py" (("from setuptools import Extension as CyExtension") "from Cython.Distutils import Extension as CyExtension") (("from setuptools.command.build_ext import build_ext as _build_ext") "from Cython.Distutils import build_ext as _build_ext") (("HAS_CYTHON = False") "HAS_CYTHON = True") (("cy_ext = 'cpp'") "cy_ext = 'pyx'")))) (add-before 'build 'build-extensions (lambda _ ;; Cython extensions have to be built before running the tests. (invoke "python" "setup.py" "build_ext" "--inplace"))) (replace 'check (lambda* (#:key tests? inputs outputs #:allow-other-keys) (when tests? (add-installed-pythonpath inputs outputs) (invoke "pytest" "-v"))))))) (native-inputs (list python-cython python-pytest python-pytest-runner)) (inputs (list zlib bzip2 seqan-1 python-screed python-bz2file)) (home-page "https://khmer.readthedocs.org/") (synopsis "K-mer counting, filtering and graph traversal library") (description "The khmer software is a set of command-line tools for working with DNA shotgun sequencing data from genomes, transcriptomes, metagenomes and single cells. Khmer can make de novo assemblies faster, and sometimes better. Khmer can also identify and fix problems with shotgun data.") ;; When building on i686, armhf and mips64el, we get the following error: ;; error: ['khmer', 'khmer.tests', 'oxli'] require 64-bit operating system (supported-systems '("x86_64-linux" "aarch64-linux")) (license license:bsd-3))) (define-public kaiju (package (name "kaiju") (version "1.9.0") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/bioinformatics-centre/kaiju") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "1hfmadkfs6jjd7l3byly5xxb0ifm3dm1wis11sjbqfcv6l89snmg")))) (build-system gnu-build-system) (arguments (list #:tests? #f ; There are no tests. #:phases #~(modify-phases %standard-phases (delete 'configure) (add-before 'build 'move-to-src-dir (lambda _ (chdir "src"))) (replace 'install (lambda _ (let ((bin (string-append #$output "/bin"))) (mkdir-p bin) (copy-recursively "../bin" bin) (let ((path (search-path-as-list '("bin") '#$(match (package-inputs this-package) (((_ pkg) ...) pkg))))) (for-each (lambda (script) (let ((exe (string-append bin "/" script))) (chmod exe #o555) (wrap-script exe #:guile #$(file-append guile-3.0 "/bin/guile") `("PATH" ":" prefix ,path)))) (list "kaiju-convertMAR.py" "kaiju-gbk2faa.pl" "kaiju-makedb"))))))))) (inputs (list bzip2 coreutils curl gawk guile-3.0 ;for wrap-script gzip perl python-wrapper tar wget zlib)) (home-page "https://kaiju.binf.ku.dk/") (synopsis "Fast and sensitive taxonomic classification for metagenomics") (description "Kaiju is a program for sensitive taxonomic classification of high-throughput sequencing reads from metagenomic whole genome sequencing experiments.") (license license:gpl3+))) (define-public macs (package (name "macs") (version "2.2.9.1") (source (origin ;; The PyPi tarball does not contain tests. (method git-fetch) (uri (git-reference (url "https://github.com/macs3-project/MACS") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "10vwc09fq4nvbd39hax1949mvq2wvkgz0k3p2zqmqwq8hv9r5l0j")) (modules '((guix build utils))) ;; Remove files generated by Cython (snippet '(begin (for-each (lambda (file) (let ((generated-file (string-append (string-drop-right file 3) "c"))) (when (file-exists? generated-file) (delete-file generated-file)))) (find-files "." "\\.pyx$")) (delete-file "MACS2/IO/CallPeakUnitPrecompiled.c") ;; Python 3.10 is in fact more recent than 3.6. (substitute* "setup.py" (("float\$sys.version\\[:3\\]\$<3.6") "False")))))) (build-system pyproject-build-system) (arguments `(#:phases (modify-phases %standard-phases (add-before 'build 'set-HOME (lambda _ (setenv "HOME" "/tmp")))))) ;; Propagate these for use of macs as a library. (propagated-inputs (list python-cython python-numpy)) (native-inputs (list python-pytest)) (home-page "https://github.com/macs3-project/MACS") (synopsis "Model based analysis for ChIP-Seq data") (description "MACS is an implementation of a ChIP-Seq analysis algorithm for identifying transcript factor binding sites named Model-based Analysis of ChIP-Seq (MACS). MACS captures the influence of genome complexity to evaluate the significance of enriched ChIP regions and it improves the spatial resolution of binding sites through combining the information of both sequencing tag position and orientation.") (license license:bsd-3))) (define-public maffilter (package (name "maffilter") (version "1.3.1") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/jydu/maffilter") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "196c16qw82niqqyzi7j1ga1n0zmir73bm26kg04m0i5aq2cpa0ml")))) (build-system cmake-build-system) (arguments (list #:tests? #false)) ;there are none (inputs (list boost bpp-core bpp-phyl bpp-phyl-omics bpp-seq bpp-seq-omics zlib)) (home-page "https://jydu.github.io/maffilter/") (synopsis "Multiple alignment format file processor") (description "MafFilter is a program dedicated to the analysis of genome alignments. It parses and manipulates @acronym{MAF, multiple alignment format} files as well as more simple fasta files. This package can be used to design a pipeline as a series of consecutive filters, each performing a dedicated analysis. Many of the filters are available, from alignment cleaning to phylogeny reconstruction and population genetics analysis. Despite various filtering options and format conversion tools, MafFilter can compute a wide range of statistics (phylogenetic trees, nucleotide diversity, inferrence of selection, etc.).") (license license:gpl3+))) (define-public mafft (package (name "mafft") (version "7.475") (source (origin (method url-fetch) (uri (string-append "https://mafft.cbrc.jp/alignment/software/mafft-" version "-without-extensions-src.tgz")) (file-name (string-append name "-" version ".tgz")) (sha256 (base32 "0i2i2m3blh2xkbkdk48hxfssks30ny0v381gdl7zwhcvp0axs26r")))) (build-system gnu-build-system) (arguments `(#:tests? #f ; no automated tests, though there are tests in the read me #:make-flags ,#~(list (string-append "PREFIX=" #$output) (string-append "BINDIR=" (string-append #$output "/bin"))) #:phases (modify-phases %standard-phases (add-after 'unpack 'enter-dir (lambda _ (chdir "core") #t)) (add-after 'enter-dir 'patch-makefile (lambda _ ;; on advice from the MAFFT authors, there is no need to ;; distribute mafft-profile, mafft-distance, or ;; mafft-homologs.rb as they are too "specialised". (substitute* "Makefile" ;; remove mafft-homologs.rb from SCRIPTS (("^SCRIPTS = mafft mafft-homologs.rb") "SCRIPTS = mafft") ;; remove mafft-homologs from MANPAGES (("^MANPAGES = mafft.1 mafft-homologs.1") "MANPAGES = mafft.1") ;; remove mafft-distance from PROGS (("^PROGS = dvtditr dndfast7 dndblast sextet5 mafft-distance") "PROGS = dvtditr dndfast7 dndblast sextet5") ;; remove mafft-profile from PROGS (("splittbfast disttbfast tbfast mafft-profile 2cl mccaskillwrap") "splittbfast disttbfast tbfast f2cl mccaskillwrap") (("^rm -f mafft-profile mafft-profile.exe") "#") (("^rm -f mafft-distance mafft-distance.exe") ")#") ;; do not install MAN pages in libexec folder (("^\t\\$\$INSTALL\$ -m 644 \\$\$MANPAGES\$ \ \\$\$DESTDIR\$\\$\$LIBDIR\$") "#")))) (add-after 'enter-dir 'patch-paths (lambda* (#:key inputs #:allow-other-keys) (substitute* '("pairash.c" "mafft.tmpl") (("perl") (which "perl")) (("([\"`| ])awk" _ prefix) (string-append prefix (which "awk"))) (("grep") (which "grep"))))) (delete 'configure) (add-after 'install 'wrap-programs (lambda* (#:key inputs outputs #:allow-other-keys) (let* ((out (assoc-ref outputs "out")) (bin (string-append out "/bin")) (path (string-append (assoc-ref inputs "coreutils") "/bin:"))) (for-each (lambda (file) (wrap-program file `("PATH" ":" prefix (,path)))) (find-files bin)))))))) (inputs (list bash-minimal perl ruby gawk grep coreutils)) (home-page "https://mafft.cbrc.jp/alignment/software/") (synopsis "Multiple sequence alignment program") (description "MAFFT offers a range of multiple alignment methods for nucleotide and protein sequences. For instance, it offers L-INS-i (accurate; for alignment of <~200 sequences) and FFT-NS-2 (fast; for alignment of <~30,000 sequences).") (license (license:non-copyleft "https://mafft.cbrc.jp/alignment/software/license.txt" "BSD-3 with different formatting")))) (define-public mash (package (name "mash") (version "2.1") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/marbl/mash") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "049hwcc059p2fd9vwndn63laifvvsi0wmv84i6y1fr79k15dxwy6")) (modules '((guix build utils))) (snippet ;; Delete bundled kseq. ;; TODO: Also delete bundled murmurhash and open bloom filter. '(delete-file "src/mash/kseq.h")))) (build-system gnu-build-system) (arguments `(#:tests? #f ; No tests. #:configure-flags ,#~(list (string-append "--with-capnp=" #$(this-package-input "capnproto")) (string-append "--with-gsl=" #$(this-package-input "gsl"))) #:make-flags (list "CC=gcc") #:phases (modify-phases %standard-phases (replace 'bootstrap ;; The bootstrap script is missing a shebang. (lambda _ (invoke "bash" "./bootstrap.sh"))) (add-after 'unpack 'fix-includes (lambda _ (substitute* '("src/mash/Sketch.cpp" "src/mash/CommandFind.cpp" "src/mash/CommandScreen.cpp") (("^#include \"kseq\\.h\"") "#include \"htslib/kseq.h\"")))) (add-after 'fix-includes 'use-c++14 (lambda _ ;; capnproto 1.0 requires c++14 to build. (substitute* (list "configure.ac" "Makefile.in") (("c\\+\\+11") "c++14"))))))) (native-inputs (list autoconf)) (inputs (list ;; Capnproto and htslib are statically embedded in the final ;; application. Therefore we also list their licenses, below. capnproto htslib gsl zlib)) (supported-systems '("x86_64-linux")) (home-page "https://mash.readthedocs.io") (synopsis "Fast genome and metagenome distance estimation using MinHash") (description "Mash is a fast sequence distance estimator that uses the MinHash algorithm and is designed to work with genomes and metagenomes in the form of assemblies or reads.") (license (list license:bsd-3 ; Mash license:expat ; HTSlib and capnproto license:public-domain ; MurmurHash 3 license:cpl1.0)))) ; Open Bloom Filter (define-public metabat (package (name "metabat") (version "2.15") (source (origin (method git-fetch) (uri (git-reference (url "https://bitbucket.org/berkeleylab/metabat.git") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "0v3gsps0ypani14102z2y1a2wignhpf7s1h45mxmj5f783rkhqd9")))) (build-system cmake-build-system) (arguments `(#:configure-flags ,#~(list (string-append "-Dzlib_LIB=" #$(this-package-input "zlib") "/lib/libz.so") (string-append "-Dhtslib_LIB=" #$(this-package-input "htslib") "/lib/libhts.so") (string-append "-DBOOST_ROOT=" #$(this-package-input "boost"))) #:phases (modify-phases %standard-phases (add-after 'unpack 'configure-version-file (lambda _ (copy-file "metabat_version.h.in" "metabat_version.h") (substitute* "metabat_version.h" (("@_time_stamp@") "19700101") (("@GIT_IS_DIRTY@") "0") (("@GIT_RETRIEVED_STATE@") "0") (("@GIT_HEAD_SHA1@") (string-append "v" ,version))))) (add-after 'unpack 'do-not-use-bundled-libraries (lambda _ (substitute* "CMakeLists.txt" (("include\\(cmake.*") "")) (substitute* "src/CMakeLists.txt" (("set\\(Boost.*") "") (("add_dependencies.*") ""))))))) (inputs (list zlib perl samtools htslib boost)) (home-page "https://bitbucket.org/berkeleylab/metabat") (synopsis "Reconstruction of single genomes from complex microbial communities") (description "Grouping large genomic fragments assembled from shotgun metagenomic sequences to deconvolute complex microbial communities, or metagenome binning, enables the study of individual organisms and their interactions. MetaBAT is an automated metagenome binning software, which integrates empirical probabilistic distances of genome abundance and tetranucleotide frequency.") ;; The source code contains inline assembly. (supported-systems '("x86_64-linux" "i686-linux")) (license (license:non-copyleft "file://license.txt" "See license.txt in the distribution.")))) (define-public metal (package (name "metal") (version "2011-03-25") (source (origin (method url-fetch) (uri (string-append "http://csg.sph.umich.edu/abecasis/Metal/" "download/generic-metal-" version ".tar.gz")) (sha256 (base32 "1bk00hc0xagmq0mabmbb8bykl75qd4kfyirba869h4x6hmn4a0f3")))) (build-system gnu-build-system) (arguments (list #:tests? #f #:make-flags #~(list (string-append "INSTALLDIR=" #$output "/bin") "all") #:phases '(modify-phases %standard-phases (replace 'configure (lambda _ (substitute* "Makefile" (("^CFLAGS=") "CFLAGS=-std=c++11 "))))))) (inputs (list zlib `(,zlib "static"))) (home-page "http://csg.sph.umich.edu/abecasis/Metal/") (synopsis "Facilitate meta-analysis of large datasets") (description "METAL is a tool for meta-analysis genomewide association scans. METAL can combine either test statistics and standard errors or p-values across studies (taking sample size and direction of effect into account). METAL analysis is a convenient alternative to a direct analysis of merged data from multiple studies. It is especially appropriate when data from the individual studies cannot be analyzed together because of differences in ethnicity, phenotype distribution, gender or constraints in sharing of individual level data imposed. Meta-analysis results in little or no loss of efficiency compared to analysis of a combined dataset including data from all individual studies.") (license license:bsd-3))) (define-public minced (package (name "minced") (version "0.3.2") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/ctSkennerton/minced") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "1f5h9him0gd355cnx7p6pnxpknhckd4g0v62mg8zyhfbx9as25fv")))) (build-system gnu-build-system) (arguments `(#:test-target "test" #:phases (modify-phases %standard-phases (delete 'configure) (add-before 'check 'fix-test (lambda _ ;; Fix test for latest version. (substitute* "t/Aquifex_aeolicus_VF5.expected" (("minced:0.1.6") "minced:0.2.0")) #t)) (replace 'install ; No install target. (lambda* (#:key inputs outputs #:allow-other-keys) (let* ((out (assoc-ref outputs "out")) (bin (string-append out "/bin")) (wrapper (string-append bin "/minced"))) ;; Minced comes with a wrapper script that tries to figure out where ;; it is located before running the JAR. Since these paths are known ;; to us, we build our own wrapper to avoid coreutils dependency. (install-file "minced.jar" bin) (with-output-to-file wrapper (lambda _ (display (string-append "#!" (assoc-ref inputs "bash") "/bin/sh\n\n" (assoc-ref inputs "jre") "/bin/java -jar " bin "/minced.jar \"$@\"\n")))) (chmod wrapper #o555)) #t))))) (native-inputs `(("jdk" ,icedtea "jdk"))) (inputs `(("bash" ,bash) ("jre" ,icedtea "out"))) (home-page "https://github.com/ctSkennerton/minced") (synopsis "Mining CRISPRs in Environmental Datasets") (description "MinCED is a program to find Clustered Regularly Interspaced Short Palindromic Repeats (CRISPRs) in DNA sequences. It can be used for unassembled metagenomic reads, but is mainly designed for full genomes and assembled metagenomic sequence.") (license license:gpl3+))) (define-public muscle (package (name "muscle") (version "3.8.1551") (source (origin (method url-fetch/tarbomb) (uri (string-append "http://www.drive5.com/muscle/muscle_src_" version ".tar.gz")) (sha256 (base32 "0bj8kj7sdizy3987zx6w7axihk40fk8rn76mpbqqjcnd64i5a367")))) (build-system gnu-build-system) (arguments `(#:make-flags (list "LDLIBS = -lm") #:phases (modify-phases %standard-phases (delete 'configure) (replace 'check ;; There are no tests, so just test if it runs. (lambda _ (invoke "./muscle" "-version") #t)) (replace 'install (lambda* (#:key outputs #:allow-other-keys) (let* ((out (assoc-ref outputs "out")) (bin (string-append out "/bin"))) (install-file "muscle" bin) #t)))))) (home-page "http://www.drive5.com/muscle") (synopsis "Multiple sequence alignment program") (description "MUSCLE aims to be a fast and accurate multiple sequence alignment program for nucleotide and protein sequences.") ;; License information found in 'muscle -h' and usage.cpp. (license license:public-domain))) (define-public music (let ((commit "b1caecdb164b1ab80acccb9463abe2526a56f69f") (revision "1")) (package (name "music") (version (git-version "0.0.0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/gersteinlab/MUSIC.git") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0arj300h8cpbya7y98g066xsxcg2a65h3y0qs250rlj072f1b4ia")))) (build-system gnu-build-system) (arguments (list #:tests? #f ; no "check" target #:phases #~(modify-phases %standard-phases (delete 'configure) ;; There is no "install" target. (replace 'install (lambda _ (let ((bin (string-append #$output "/bin"))) (install-file "bin/MUSIC" bin))))))) (home-page "https://github.com/gersteinlab/MUSIC/") (synopsis "Multiscale enrichment calling for ChIP-Seq datasets") (description "MUSIC is an algorithm for identification of enriched regions at multiple scales in the read depth signals from ChIP-Seq experiments.") ;; See https://github.com/gersteinlab/MUSIC/issues/6 (license license:gpl2+)))) (define-public newick-utils ;; There are no recent releases so we package from git. (let ((commit "da121155a977197cab9fbb15953ca1b40b11eb87")) (package (name "newick-utils") (version (string-append "1.6-1." (string-take commit 8))) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/tjunier/newick_utils") (commit commit))) (file-name (string-append name "-" version "-checkout")) (sha256 (base32 "1hkw21rq1mwf7xp0rmbb2gqc0i6p11108m69i7mr7xcjl268pxnb")))) (build-system gnu-build-system) (arguments `(#:tests? ,(not (or (target-riscv64?) ;XXX: stuck on riscv64-linux (%current-target-system))) #:make-flags (list "CFLAGS=-O2 -g -fcommon"))) (inputs ;; XXX: TODO: Enable Lua and Guile bindings. ;; https://github.com/tjunier/newick_utils/issues/13 (list libxml2 flex bison)) (native-inputs (list autoconf automake libtool)) (synopsis "Programs for working with newick format phylogenetic trees") (description "Newick-utils is a suite of utilities for processing phylogenetic trees in Newick format. Functions include re-rooting, extracting subtrees, trimming, pruning, condensing, drawing (ASCII graphics or SVG).") (home-page "https://github.com/tjunier/newick_utils") (license license:bsd-3)))) (define-public orfm (package (name "orfm") (version "0.7.1") (source (origin (method url-fetch) (uri (string-append "https://github.com/wwood/OrfM/releases/download/v" version "/orfm-" version ".tar.gz")) (sha256 (base32 "16iigyr2gd8x0imzkk1dr3k5xsds9bpmwg31ayvjg0f4pir9rwqr")))) (build-system gnu-build-system) (inputs (list zlib)) (native-inputs (list ruby-bio-commandeer ruby-rspec ruby)) (synopsis "Simple and not slow open reading frame (ORF) caller") (description "An ORF caller finds stretches of DNA that, when translated, are not interrupted by stop codons. OrfM finds and prints these ORFs.") (home-page "https://github.com/wwood/OrfM") (license license:lgpl3+))) (define-public prank (package (name "prank") (version "170427") (source (origin (method url-fetch) (uri (string-append "http://wasabiapp.org/download/prank/prank.source." version ".tgz")) (sha256 (base32 "0nc8g9c5rkdxcir46s0in9ci1sxwzbjibxrvkksf22ybnplvagk2")))) (build-system gnu-build-system) (arguments `(#:phases (modify-phases %standard-phases (add-after 'unpack 'enter-src-dir (lambda _ (chdir "src"))) (add-after 'unpack 'remove-m64-flag ;; Prank will build with the correct 'bit-ness' without this flag ;; and this allows building on 32-bit machines. (lambda _ (substitute* "src/Makefile" (("-m64") "")))) (delete 'configure) (replace 'install (lambda* (#:key inputs outputs #:allow-other-keys) (let* ((out (assoc-ref outputs "out")) (bin (string-append out "/bin")) (man (string-append out "/share/man/man1")) (path (string-append (assoc-ref inputs "mafft") "/bin:" (assoc-ref inputs "exonerate") "/bin:" (assoc-ref inputs "bppsuite") "/bin"))) (install-file "prank" bin) (wrap-program (string-append bin "/prank") `("PATH" ":" prefix (,path))) (install-file "prank.1" man))))))) (inputs (list mafft exonerate bppsuite)) (home-page "http://wasabiapp.org/software/prank/") (synopsis "Probabilistic multiple sequence alignment program") (description "PRANK is a probabilistic multiple sequence alignment program for DNA, codon and amino-acid sequences. It is based on a novel algorithm that treats insertions correctly and avoids over-estimation of the number of deletion events. In addition, PRANK borrows ideas from maximum likelihood methods used in phylogenetics and correctly takes into account the evolutionary distances between sequences. Lastly, PRANK allows for defining a potential structure for sequences to be aligned and then, simultaneously with the alignment, predicts the locations of structural units in the sequences.") (license license:gpl2+))) (define-public proteinortho (package (name "proteinortho") (version "6.3.2") (source (origin (method git-fetch) (uri (git-reference (url "https://gitlab.com/paulklemm_PHD/proteinortho.git") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "0p8iaxq193fh67hw3cydvdah1vz1c3f18227gj1mhkww0ms7g6xa")) (modules '((guix build utils))) (snippet '(begin ;; Remove pre-built scripts and source tarballs. (delete-file-recursively "src/BUILD/") (delete-file "src/lapack-3.8.0.tar.gz"))))) (build-system gnu-build-system) (arguments (list #:test-target "test" #:parallel-tests? #f #:make-flags #~(list (string-append "CC=" #$(cc-for-target)) (string-append "CXX=" #$(cxx-for-target)) (string-append "PREFIX=" #$output) (string-append "INSTALLDIR=" #$output "/bin")) #:phases #~(modify-phases %standard-phases (delete 'configure) (add-before 'install 'make-install-directory ;; The install directory is not created during 'make install'. (lambda* (#:key outputs #:allow-other-keys) (mkdir-p (string-append (assoc-ref outputs "out") "/bin")))) (add-after 'install 'wrap-programs (lambda* (#:key inputs outputs #:allow-other-keys) (let ((path (getenv "PATH")) (out (assoc-ref outputs "out")) (guile (search-input-file inputs "bin/guile"))) (for-each (lambda (script) (wrap-script script #:guile guile `("PATH" ":" prefix (,path)))) (cons (string-append out "/bin/proteinortho") (find-files out "\\.(pl|py)$"))))))))) (inputs (list bash-minimal guile-3.0 ; for wrap-script diamond perl python-wrapper blast+ openblas)) (native-inputs (list which)) (home-page "https://www.bioinf.uni-leipzig.de/Software/proteinortho") (synopsis "Detect orthologous genes across species") (description "Proteinortho is a tool to detect orthologous genes across different species. For doing so, it compares similarities of given gene sequences and clusters them to find significant groups. The algorithm was designed to handle large-scale data and can be applied to hundreds of species at once.") (properties `((tunable? . #t))) (license license:gpl3+))) (define-public prodigal (package (name "prodigal") ;; Check for a new home page when updating this package: ;; https://github.com/hyattpd/Prodigal/issues/36#issuecomment-536617588 (version "2.6.3") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/hyattpd/Prodigal") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "1fs1hqk83qjbjhrvhw6ni75zakx5ki1ayy3v6wwkn3xvahc9hi5s")))) (build-system gnu-build-system) (arguments `(#:tests? #f ; no check target #:make-flags ,#~(list (string-append "INSTALLDIR=" #$output "/bin")) #:phases (modify-phases %standard-phases (delete 'configure)))) (home-page "https://github.com/hyattpd/Prodigal") (synopsis "Protein-coding gene prediction for Archaea and Bacteria") (description "Prodigal runs smoothly on finished genomes, draft genomes, and metagenomes, providing gene predictions in GFF3, Genbank, or Sequin table format. It runs quickly, in an unsupervised fashion, handles gaps, handles partial genes, and identifies translation initiation sites.") (license license:gpl3+))) (define-public roary (package (name "roary") (version "3.12.0") (source (origin (method url-fetch) (uri (string-append "mirror://cpan/authors/id/A/AJ/AJPAGE/Bio-Roary-" version ".tar.gz")) (sha256 (base32 "0qxrds9wx7cfhlkihrp6697kx0flhhxymap9fwan0b3rbdhcnmff")))) (build-system perl-build-system) (arguments `(#:phases (modify-phases %standard-phases (delete 'configure) (delete 'build) (replace 'check (lambda _ ;; The tests are not run by default, so we run each test file ;; directly. (setenv "PATH" (string-append (getcwd) "/bin" ":" (getenv "PATH"))) (setenv "PERL5LIB" (string-append (getcwd) "/lib" ":" (getenv "PERL5LIB"))) (for-each (lambda (file) (display file)(display "\n") (invoke "perl" file)) (find-files "t" ".*\\.t$")))) (replace 'install ;; There is no 'install' target in the Makefile. (lambda* (#:key outputs #:allow-other-keys) (let* ((out (assoc-ref outputs "out")) (bin (string-append out "/bin")) (perl (string-append out "/lib/perl5/site_perl")) (roary-plots "contrib/roary_plots")) (mkdir-p bin) (mkdir-p perl) (copy-recursively "bin" bin) (copy-recursively "lib" perl)))) (add-after 'install 'wrap-programs (lambda* (#:key inputs outputs #:allow-other-keys) (let* ((out (assoc-ref outputs "out")) (perl5lib (getenv "PERL5LIB")) (path (getenv "PATH"))) (for-each (lambda (prog) (let ((binary (string-append out "/" prog))) (wrap-program binary `("PERL5LIB" ":" prefix (,(string-append perl5lib ":" out "/lib/perl5/site_perl")))) (wrap-program binary `("PATH" ":" prefix (,(string-append path ":" out "/bin")))))) (find-files "bin" ".*[^R]$")) (let ((file (string-append out "/bin/roary-create_pan_genome_plots.R")) (r-site-lib (getenv "R_LIBS_SITE")) (coreutils-path (dirname (search-input-file inputs "bin/chmod")))) (wrap-program file `("R_LIBS_SITE" ":" prefix (,(string-append r-site-lib ":" out "/site-library/")))) (wrap-program file `("PATH" ":" prefix (,(string-append coreutils-path ":" out "/bin"))))))))))) (native-inputs (list perl-env-path perl-test-files perl-test-most perl-test-output)) (inputs (list bash-minimal perl-array-utils bioperl-minimal perl-digest-md5-file perl-exception-class perl-file-find-rule perl-file-grep perl-file-slurper perl-file-which perl-graph perl-graph-readwrite perl-log-log4perl perl-moose perl-perlio-utf8_strict perl-text-csv bedtools cd-hit blast+ mcl parallel prank mafft fasttree grep sed gawk r-minimal r-ggplot2 coreutils)) (home-page "https://sanger-pathogens.github.io/Roary/") (synopsis "High speed stand-alone pan genome pipeline") (description "Roary is a high speed stand alone pan genome pipeline, which takes annotated assemblies in GFF3 format (produced by the Prokka program) and calculates the pan genome. Using a standard desktop PC, it can analyse datasets with thousands of samples, without compromising the quality of the results. 128 samples can be analysed in under 1 hour using 1 GB of RAM and a single processor. Roary is not intended for metagenomics or for comparing extremely diverse sets of genomes.") (license license:gpl3))) (define-public raxml (package (name "raxml") (version "8.2.12") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/stamatak/standard-RAxML") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "1jqjzhch0rips0vp04prvb8vmc20c5pdmsqn8knadcf91yy859fh")))) (build-system gnu-build-system) (arguments `(#:tests? #f ; There are no tests. ;; Use 'standard' Makefile rather than SSE or AVX ones. #:make-flags (list "-f" "Makefile.HYBRID.gcc") #:phases (modify-phases %standard-phases (delete 'configure) (replace 'install (lambda* (#:key outputs #:allow-other-keys) (let* ((out (assoc-ref outputs "out")) (bin (string-append out "/bin")) (executable "raxmlHPC-HYBRID")) (install-file executable bin) (symlink (string-append bin "/" executable) "raxml")) #t))))) (inputs (list openmpi)) (home-page "https://cme.h-its.org/exelixis/web/software/raxml/index.html") (synopsis "Randomized Axelerated Maximum Likelihood phylogenetic trees") (description "RAxML is a tool for phylogenetic analysis and post-analysis of large phylogenies.") ;; The source includes x86 specific code (supported-systems '("x86_64-linux" "i686-linux")) (license license:gpl2+))) (define-public rsem (package (name "rsem") (version "1.3.3") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/deweylab/RSEM") (commit (string-append "v" version)))) (sha256 (base32 "1yl4i7z20n2p84j1lmk15aiak3yqc6fiw0q5a4pndw7pxfiq3rzp")) (file-name (git-file-name name version)) (modules '((guix build utils))) (snippet '(begin ;; remove bundled copy of boost and samtools (delete-file-recursively "boost") (delete-file-recursively "samtools-1.3"))))) (build-system gnu-build-system) (arguments `(#:tests? #f ;no "check" target #:make-flags ,#~(list (string-append "BOOST=" #$(this-package-input "boost") "/include/") (string-append "SAMHEADERS=" #$(this-package-input "htslib") "/include/htslib/sam.h") (string-append "SAMLIBS=" #$(this-package-input "htslib") "/lib/libhts.so")) #:phases (modify-phases %standard-phases ;; No "configure" script. (replace 'configure (lambda _ (substitute* "Makefile" (("^all : \\$\$PROGRAMS\$.*") "all: $(PROGRAMS)\n") ;; Do not build bundled samtools library. (("^\\$\$SAMLIBS\$.*") "") ;; Needed for Boost (("gnu\\+\\+98") "gnu++11")) ;; C++11 compatibility (substitute* "buildReadIndex.cpp" (("success = \\(getline") "success = (bool)(getline")) (substitute* '("PairedEndHit.h" "SingleHit.h") (("return \\(in>>sid>>pos") "return (bool)(in>>sid>>pos")))) (replace 'install (lambda* (#:key outputs #:allow-other-keys) (let* ((out (string-append (assoc-ref outputs "out"))) (bin (string-append out "/bin/")) (perl (string-append out "/lib/perl5/site_perl"))) (mkdir-p bin) (mkdir-p perl) (for-each (lambda (file) (install-file file bin)) (find-files "." "rsem-.*")) (install-file "rsem_perl_utils.pm" perl)))) (add-after 'install 'wrap-program (lambda* (#:key outputs #:allow-other-keys) (let ((out (assoc-ref outputs "out"))) (for-each (lambda (prog) (wrap-program (string-append out "/bin/" prog) `("PERL5LIB" ":" prefix (,(string-append out "/lib/perl5/site_perl"))))) '("rsem-calculate-expression" "rsem-control-fdr" "rsem-generate-data-matrix" "rsem-generate-ngvector" "rsem-plot-transcript-wiggles" "rsem-prepare-reference" "rsem-run-ebseq" "rsem-run-prsem-testing-procedure")))))))) (inputs (list bash-minimal boost r-minimal perl htslib-1.3 zlib)) (home-page "https://deweylab.biostat.wisc.edu/rsem/") (synopsis "Estimate gene expression levels from RNA-Seq data") (description "RSEM is a software package for estimating gene and isoform expression levels from RNA-Seq data. The RSEM package provides a user-friendly interface, supports threads for parallel computation of the EM algorithm, single-end and paired-end read data, quality scores, variable-length reads and RSPD estimation. In addition, it provides posterior mean and 95% credibility interval estimates for expression levels. For visualization, it can generate BAM and Wiggle files in both transcript-coordinate and genomic-coordinate.") (license license:gpl3+))) (define-public rseqc (package (name "rseqc") (version "3.0.1") (source (origin (method url-fetch) (uri (string-append "mirror://sourceforge/rseqc/" "RSeQC-" version ".tar.gz")) (sha256 (base32 "0gbb9iyb7swiv5455fm5rg98r7l6qn27v564yllqjd574hncpx6m")))) (build-system python-build-system) (inputs (list python-cython python-bx-python python-pybigwig python-pysam python-numpy zlib)) (native-inputs (list python-nose)) (home-page "https://rseqc.sourceforge.net/") (synopsis "RNA-seq quality control package") (description "RSeQC provides a number of modules that can comprehensively evaluate high throughput sequence data, especially RNA-seq data. Some basic modules inspect sequence quality, nucleotide composition bias, PCR bias and GC bias, while RNA-seq specific modules evaluate sequencing saturation, mapped reads distribution, coverage uniformity, strand specificity, etc.") (license license:gpl3+))) (define-public seek ;; There are no release tarballs. And the installation instructions at ;; http://seek.princeton.edu/installation.jsp only mention a mercurial ;; changeset ID. This is a git repository, though. So we just take the ;; most recent commit. (let ((commit "196ed4c7633246e9c628e4330d77577ccfd7f1e5") (revision "1")) (package (name "seek") (version (git-version "1" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/FunctionLab/sleipnir.git") (commit commit) (recursive? #true))) (file-name (git-file-name name version)) (sha256 (base32 "0c658n8nz563a96dsi4gl2685vxph0yfmmqq5yjc6i4xin1jy1ab")))) (build-system cmake-build-system) (arguments `(#:configure-flags ,#~(list (string-append "-DSVM_LIBRARY=" #$(this-package-input "libsvm") "/lib/libsvm.so.2") (string-append "-DSVM_INCLUDE=" #$(this-package-input "libsvm") "/include")) #:tests? #false ; tests only fail in the build container #:phases (modify-phases %standard-phases ;; The check phase expects to find the unit_tests executable in the ;; "build/bin" directory, but it is actually in "build/tests". (replace 'check (lambda* (#:key tests? #:allow-other-keys) (when tests? (invoke "tests/unit_tests"))))))) (inputs `(("apache-thrift:include" ,apache-thrift "include") ("apache-thrift:lib" ,apache-thrift "lib") ("gsl" ,gsl) ("boost" ,boost) ("gengetopt" ,gengetopt) ("libsvm" ,libsvm) ("log4cpp" ,log4cpp) ("python" ,python) ("readline" ,readline))) (native-inputs (list pkg-config)) (home-page "https://seek.princeton.edu") (synopsis "Gene co-expression search engine") (description "SEEK is a computational gene co-expression search engine. SEEK provides biologists with a way to navigate the massive human expression compendium that now contains thousands of expression datasets. SEEK returns a robust ranking of co-expressed genes in the biological area of interest defined by the user's query genes. It also prioritizes thousands of expression datasets according to the user's query of interest.") (license license:cc-by3.0)))) (define-public samtools (package (name "samtools") (version "1.19") (source (origin (method url-fetch) (uri (string-append "https://github.com/samtools/samtools" "/releases/download/" version "/samtools-" version ".tar.bz2")) (sha256 (base32 "10wby07w33rfypy4kf73v9wwnbyh0lrazbsmrgrvcl88w8c3nszs")) (modules '((guix build utils))) ;; Delete bundled htslib. (snippet '(delete-file-recursively "htslib-1.19")))) (build-system gnu-build-system) (arguments `(#:configure-flags (list "--with-ncurses") ;; The samtools test suite (and software) expects SSE-based math, even on ;; i686-linux, and not 387-based math. Adjust the CPPFLAGS accordingly. ,@(if (target-x86-32?) `(#:make-flags (list "CPPFLAGS = -msse -mfpmath=sse")) '()) #:phases (modify-phases %standard-phases (add-after 'unpack 'patch-tests (lambda _ (substitute* "test/test.pl" ;; The test script calls out to /bin/bash (("/bin/bash") (which "bash")))))))) (native-inputs (list pkg-config)) (inputs (list htslib ncurses perl python zlib)) (home-page "https://samtools.sourceforge.net") (synopsis "Utilities to efficiently manipulate nucleotide sequence alignments") (description "Samtools implements various utilities for post-processing nucleotide sequence alignments in the SAM, BAM, and CRAM formats, including indexing, variant calling (in conjunction with bcftools), and a simple alignment viewer.") (license license:expat))) (define-public samtools-1.14 (package/inherit samtools (version "1.14") (source (origin (method url-fetch) (uri (string-append "mirror://sourceforge/samtools/samtools/" version "/samtools-" version ".tar.bz2")) (sha256 (base32 "0x3xdda78ac5vx66b3jdsv9sfhyz4npl4znl1zbaf3lbm6xdlhck")) (modules '((guix build utils))) (snippet '(begin ;; Delete bundled htslib. (delete-file-recursively "htslib-1.14"))))) (native-inputs (list pkg-config)) (inputs (list htslib-1.14 ncurses perl python zlib)))) (define-public samtools-1.12 (package/inherit samtools (version "1.12") (source (origin (method url-fetch) (uri (string-append "mirror://sourceforge/samtools/samtools/" version "/samtools-" version ".tar.bz2")) (sha256 (base32 "1jrdj2idpma5ja9cg0rr73b565vdbr9wyy6zig54bidicc2pg8vd")) (modules '((guix build utils))) (snippet '(begin ;; Delete bundled htslib. (delete-file-recursively "htslib-1.12"))))) (arguments (substitute-keyword-arguments (package-arguments samtools) ((#:modules _ #f) '((ice-9 ftw) (ice-9 regex) (guix build gnu-build-system) (guix build utils))) ((#:phases phases) `(modify-phases ,phases (add-after 'install 'install-library (lambda* (#:key outputs #:allow-other-keys) (let ((lib (string-append (assoc-ref outputs "out") "/lib"))) (install-file "libbam.a" lib)))) (add-after 'install 'install-headers (lambda* (#:key outputs #:allow-other-keys) (let ((include (string-append (assoc-ref outputs "out") "/include/samtools/"))) (for-each (lambda (file) (install-file file include)) (scandir "." (lambda (name) (string-match "\\.h$" name))))))))))) (native-inputs (list pkg-config)) (inputs (list htslib-1.12 ncurses perl python zlib)))) (define-public samtools-1.10 (package (inherit samtools) (name "samtools") (version "1.10") (source (origin (method url-fetch) (uri (string-append "mirror://sourceforge/samtools/samtools/" version "/samtools-" version ".tar.bz2")) (sha256 (base32 "119ms0dpydw8dkh3zc4yyw9zhdzgv12px4l2kayigv31bpqcb7kv")) (modules '((guix build utils))) (snippet '(begin ;; Delete bundled htslib. (delete-file-recursively "htslib-1.10") #t)))) (inputs (list htslib-1.10 ncurses perl python zlib)))) (define-public samtools-1.2 (package (inherit samtools) (name "samtools") (version "1.2") (source (origin (method url-fetch) (uri (string-append "mirror://sourceforge/samtools/samtools/" version "/samtools-" version ".tar.bz2")) (sha256 (base32 "1akdqb685pk9xk1nb6sa9aq8xssjjhvvc06kp4cpdqvz2157l3j2")) (modules '((guix build utils))) (snippet ;; Delete bundled htslib and Windows binaries '(for-each delete-file-recursively (list "win32" "htslib-1.2.1"))))) (arguments `(#:make-flags ,#~(list (string-append "prefix=" #$output) (string-append "BGZIP=" #$(this-package-input "htslib") "/bin/bgzip") (string-append "HTSLIB=" #$(this-package-input "htslib") "/lib/libhts.so") (string-append "HTSDIR=" #$(this-package-input "htslib") "/include")) #:phases (modify-phases %standard-phases (add-after 'unpack 'patch-makefile-curses (lambda _ (substitute* "Makefile" (("-lcurses") "-lncurses") (("include \\$\$HTSDIR.*") "")))) (add-after 'unpack 'patch-tests (lambda _ (substitute* "test/test.pl" ;; The test script calls out to /bin/bash (("/bin/bash") (which "bash")) ;; There are two failing tests upstream relating to the "stats" ;; subcommand in test_usage_subcommand ("did not have Usage" ;; and "usage did not mention samtools stats"), so we disable ;; them. (("(test_usage_subcommand\\(.*\$;)" cmd) (string-append "unless ($subcommand eq 'stats') {" cmd "};"))) ;; This test fails because the grep output doesn't look as ;; expected; it is correct, though. (substitute* "test/mpileup/mpileup.reg" (("P 52.out.*") "")))) (delete 'configure)))) (native-inputs (list grep gawk pkg-config)) (inputs (list htslib-for-samtools-1.2 ncurses perl python zlib)))) (define-public samtools-0.1 ;; This is the most recent version of the 0.1 line of samtools. The input ;; and output formats differ greatly from that used and produced by samtools ;; 1.x and is still used in many bioinformatics pipelines. (package (inherit samtools) (version "0.1.19") (source (origin (method url-fetch) (uri (string-append "mirror://sourceforge/samtools/samtools/" version "/samtools-" version ".tar.bz2")) (sha256 (base32 "1m33xsfwz0s8qi45lylagfllqg7fphf4dr0780rsvw75av9wk06h")))) (arguments `(#:tests? #f ;no "check" target #:make-flags (list "LIBCURSES=-lncurses") ,@(substitute-keyword-arguments (package-arguments samtools) ((#:modules _ #f) '((ice-9 ftw) (ice-9 regex) (guix build gnu-build-system) (guix build utils))) ((#:phases phases) `(modify-phases ,phases (replace 'install (lambda* (#:key outputs #:allow-other-keys) (let ((bin (string-append (assoc-ref outputs "out") "/bin"))) (mkdir-p bin) (install-file "samtools" bin) #t))) (add-after 'install 'install-library (lambda* (#:key outputs #:allow-other-keys) (let ((lib (string-append (assoc-ref outputs "out") "/lib"))) (install-file "libbam.a" lib)))) (add-after 'install 'install-headers (lambda* (#:key outputs #:allow-other-keys) (let ((include (string-append (assoc-ref outputs "out") "/include/samtools/"))) (for-each (lambda (file) (install-file file include)) (scandir "." (lambda (name) (string-match "\\.h$" name))))))) (delete 'patch-tests) (delete 'configure)))))))) (define-public savvy (package (name "savvy") (version "2.1.0") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/statgen/savvy") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "03jh89gl67adnpkwx8yrdn62pd9sg69k21gxh15my2vvpfl1pxlx")))) (build-system cmake-build-system) (arguments (list #:configure-flags '(list "-DBUILD_TESTS=ON" "-DBUILD_EVAL=ON") #:phases '(modify-phases %standard-phases (add-after 'unpack 'use-shared-libraries (lambda _ ;; Do not prefer static libraries. (substitute* "CMakeLists.txt" (("set\\(CMAKE_FIND_LIBRARY_SUFFIXES \".a;.*") ""))))))) (native-inputs (list pkg-config)) (inputs (list htslib)) (propagated-inputs (list streambuf-shrinkwrap)) (home-page "https://github.com/statgen/savvy/") (synopsis "Interface to various variant calling formats") (description "Savvy is the official C++ interface for the SAV file format and offers seamless support for BCF and VCF files.") (license license:mpl2.0))) (define-public morpheus (package (name "morpheus") (version "2.3.6") (source (origin (method git-fetch) (uri (git-reference (url "https://gitlab.com/morpheus.lab/morpheus") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "1jyzbkz8d39kjicrk3ihcx7yvq5wsynvnlcw922bqqsw8nwnn12c")) (modules '((guix build utils))) (snippet '(begin (delete-file-recursively "3rdparty/eigen") (substitute* '("morpheus/core/cpm_shape_tracker.cpp" "morpheus/core/membranemapper.h" "morpheus/testing/components/motility/directed_motion_test.cpp" "morpheus/testing/components/interaction/generator_cell_sorting.cpp" "morpheus/testing/components/interaction/test_cell_sorting.cpp" "morpheus/testing/core/cpm/generator_csm_plane.cpp" "morpheus/testing/test_operators.h") (("#include \"eigen/") "#include \"eigen3/")))))) ;; This is for a different Morpheus. (properties '((lint-hidden-cve "CVE-2022-31261"))) (build-system cmake-build-system) (arguments (list #:configure-flags '(list "-DMORPHEUS_GUI=OFF" "-DBUILD_TESTING=ON" "-DDOWNLOAD_XTENSOR=OFF") #:phases '(modify-phases %standard-phases (add-after 'unpack 'disable-gtest-download (lambda _ (substitute* "3rdparty/CMakeLists.txt" (("add_subdirectory\$GTest\$") "")))) (replace 'check (lambda* (#:key tests? #:allow-other-keys) (when tests? (invoke "ctest" "--output-junit" "test_results.xml"))))))) (inputs (list boost eigen file gnuplot libtiff libxslt xsimd xtensor xtl zlib)) (native-inputs (list doxygen googletest xxd)) (home-page "https://gitlab.com/morpheus.lab/morpheus") (synopsis "Multicellular simulation") (description "Morpheus is a modeling and simulation environment for the study of multi-scale and multicellular systems.") (license license:bsd-3))) (define-public mosaik (let ((commit "5c25216d3522d6a33e53875cd76a6d65001e4e67")) (package (name "mosaik") (version "2.2.30") (source (origin ;; There are no release tarballs nor tags. (method git-fetch) (uri (git-reference (url "https://github.com/wanpinglee/MOSAIK") (commit commit))) (file-name (string-append name "-" version)) (sha256 (base32 "17gj3s07cm77r41z92awh0bim7w7q7fbn0sf5nkqmcm1vw052qgw")))) (build-system gnu-build-system) (arguments `(#:tests? #f ; no tests #:make-flags (list "CC=gcc") #:phases (modify-phases %standard-phases (replace 'configure (lambda _ (chdir "src") #t)) (replace 'install (lambda* (#:key outputs #:allow-other-keys) (let ((bin (string-append (assoc-ref outputs "out") "/bin"))) (mkdir-p bin) (copy-recursively "../bin" bin) #t)))))) (inputs `(("perl" ,perl) ("zlib:static" ,zlib "static") ("zlib" ,zlib))) (supported-systems '("x86_64-linux")) (home-page "https://github.com/wanpinglee/MOSAIK") (synopsis "Map nucleotide sequence reads to reference genomes") (description "MOSAIK is a program for mapping second and third-generation sequencing reads to a reference genome. MOSAIK can align reads generated by all the major sequencing technologies, including Illumina, Applied Biosystems SOLiD, Roche 454, Ion Torrent and Pacific BioSciences SMRT.") ;; MOSAIK is released under the GPLv2+ with the exception of third-party ;; code released into the public domain: ;; 1. fastlz by Ariya Hidayat - http://www.fastlz.org/ ;; 2. MD5 implementation - RSA Data Security, RFC 1321 (license (list license:gpl2+ license:public-domain))))) (define-public mosaicatcher (package (name "mosaicatcher") (version "0.3.1") (source (origin ;; There are no release tarballs nor tags. (method git-fetch) (uri (git-reference (url "https://github.com/friendsofstrandseq/mosaicatcher") (commit (string-append version "-dev")))) (file-name (git-file-name name version)) (sha256 (base32 "1n2s5wvvj2y0vfgjkg1q11xahpbagxz7h2vf5q7qyy25s12kbzbd")) (patches (search-patches "mosaicatcher-unbundle-htslib.patch")))) (build-system cmake-build-system) (arguments `(#:tests? #false ; there are no tests #:phases (modify-phases %standard-phases (add-after 'unpack 'chdir (lambda _ (chdir "src"))) (replace 'install (lambda* (#:key inputs outputs #:allow-other-keys) (let* ((target (assoc-ref outputs "out")) (bin (string-append target "/bin")) (share (string-append target "/share/mosaicatcher"))) (install-file "mosaic" bin) (mkdir-p share) (copy-recursively "../R" share))))))) (inputs (list boost htslib)) (home-page "https://github.com/friendsofstrandseq/mosaicatcher") (synopsis "Count and classify Strand-seq reads") (description "Mosaicatcher counts Strand-seq reads and classifies strand states of each chromosome in each cell using a Hidden Markov Model.") (license license:expat))) (define-public ngs-sdk (package (name "ngs-sdk") (version "2.10.5") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/ncbi/ngs") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "1ix51c25hjn57w93qmwzw80xh2i34wx8j2hn7szh8p6w8i3az5qa")))) (build-system gnu-build-system) (arguments `(#:parallel-build? #f ; not supported #:tests? #f ; no "check" target #:phases (modify-phases %standard-phases (replace 'configure (lambda* (#:key outputs #:allow-other-keys) (let ((out (assoc-ref outputs "out"))) ;; Allow 'konfigure.perl' to find 'package.prl'. (setenv "PERL5LIB" (string-append ".:" (getenv "PERL5LIB"))) ;; The 'configure' script doesn't recognize things like ;; '--enable-fast-install'. (invoke "./configure" (string-append "--build-prefix=" (getcwd) "/build") (string-append "--prefix=" out)) #t))) (add-after 'unpack 'enter-dir (lambda _ (chdir "ngs-sdk") #t))))) (native-inputs (list perl)) ;; According to the test ;; unless ($MARCH =~ /x86_64/i || $MARCH =~ /i?86/i) ;; in ngs-sdk/setup/konfigure.perl (supported-systems '("i686-linux" "x86_64-linux")) (home-page "https://github.com/ncbi/ngs") (synopsis "API for accessing Next Generation Sequencing data") (description "NGS is a domain-specific API for accessing reads, alignments and pileups produced from Next Generation Sequencing. The API itself is independent from any particular back-end implementation, and supports use of multiple back-ends simultaneously.") (license license:public-domain))) (define-public java-ngs (package (inherit ngs-sdk) (name "java-ngs") (arguments `(,@(substitute-keyword-arguments `(#:modules ((guix build gnu-build-system) (guix build utils) (srfi srfi-1) (srfi srfi-26)) ,@(package-arguments ngs-sdk)) ((#:phases phases) `(modify-phases ,phases (replace 'enter-dir (lambda _ (chdir "ngs-java") #t))))))) (inputs `(("jdk" ,icedtea "jdk") ("ngs-sdk" ,ngs-sdk))) (synopsis "Java bindings for NGS SDK"))) (define-public ncbi-vdb (package (name "ncbi-vdb") (version "2.10.6") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/ncbi/ncbi-vdb") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "0m8hlxscidsfqm9x9fyi62q6lpf1dv5115kgjjgnrkl49q9c27m6")))) (build-system gnu-build-system) (arguments (list #:parallel-build? #f ; not supported #:tests? #f ; no "check" target #:make-flags '(list "HAVE_HDF5=1") #:phases #~(modify-phases %standard-phases #; (add-after 'unpack 'make-files-writable (lambda _ (for-each make-file-writable (find-files "." ".*")))) (add-before 'configure 'set-perl-search-path (lambda _ ;; Work around "dotless @INC" build failure. (setenv "PERL5LIB" (string-append (getcwd) "/setup:" (getenv "PERL5LIB"))))) ;; See https://github.com/ncbi/ncbi-vdb/issues/14 (add-after 'unpack 'patch-krypto-flags (lambda _ (substitute* "libs/krypto/Makefile" (("-Wa,-march=generic64\\+aes") "") (("-Wa,-march=generic64\\+sse4") "")))) (replace 'configure (lambda _ ;; Override include path for libmagic (substitute* "setup/package.prl" (("name => 'magic', Include => '/usr/include'") (string-append "name=> 'magic', Include => '" #$(this-package-input "file") "/include" "'"))) ;; Install kdf5 library (needed by sra-tools) (substitute* "build/Makefile.install" (("LIBRARIES_TO_INSTALL =") "LIBRARIES_TO_INSTALL = kdf5.$(VERSION_LIBX) kdf5.$(VERSION_SHLX)")) (substitute* "build/Makefile.env" (("CFLAGS =" prefix) (string-append prefix "-msse2 "))) ;; Override search path for ngs-java (substitute* "setup/package.prl" (("/usr/local/ngs/ngs-java") #$(this-package-input "java-ngs"))) ;; The 'configure' script doesn't recognize things like ;; '--enable-fast-install'. (invoke "./configure" (string-append "--build-prefix=" (getcwd) "/build") (string-append "--prefix=" #$output) (string-append "--debug") (string-append "--with-xml2-prefix=" #$(this-package-input "libxml2")) (string-append "--with-ngs-sdk-prefix=" #$(this-package-input "ngs-sdk")) (string-append "--with-hdf5-prefix=" #$(this-package-input "hdf5"))))) (add-after 'install 'install-interfaces (lambda _ ;; Install interface libraries. On i686 the interface libraries ;; are installed to "linux/gcc/i386", so we need to use the Linux ;; architecture name ("i386") instead of the target system prefix ;; ("i686"). (mkdir (string-append #$output "/ilib")) (copy-recursively (string-append "build/ncbi-vdb/linux/gcc/" #$(platform-linux-architecture (lookup-platform-by-target-or-system (or (%current-target-system) (%current-system)))) "/rel/ilib") (string-append #$output "/ilib")) ;; Install interface headers (copy-recursively "interfaces" (string-append #$output "/include")))) (add-after 'install-interfaces 'install-libs (lambda _ (copy-recursively (string-append "build/ncbi-vdb/linux/gcc/" #$(platform-linux-architecture (lookup-platform-by-target-or-system (or (%current-target-system) (%current-system)))) "/rel/lib") (string-append #$output "/lib")))) ;; These files are needed by sra-tools. (add-after 'install 'install-configuration-files (lambda _ (let ((target (string-append #$output "/kfg"))) (mkdir target) (install-file "libs/kfg/default.kfg" target) (install-file "libs/kfg/certs.kfg" target))))))) (inputs (list file hdf5 java-ngs libxml2 ngs-sdk )) (native-inputs (list perl)) ;; NCBI-VDB requires SSE capability. (supported-systems '("i686-linux" "x86_64-linux")) (home-page "https://github.com/ncbi/ncbi-vdb") (synopsis "Database engine for genetic information") (description "The NCBI-VDB library implements a highly compressed columnar data warehousing engine that is most often used to store genetic information. Databases are stored in a portable image within the file system, and can be accessed/downloaded on demand across HTTP.") (license license:public-domain))) (define-public plink (package (name "plink") (version "1.07") (source (origin (method url-fetch) (uri (string-append "https://zzz.bwh.harvard.edu/plink/dist/plink-" version "-src.zip")) (sha256 (base32 "0as8gxm4pjyc8dxmm1sl873rrd7wn5qs0l29nqfnl31x8i467xaa")) (patches (search-patches "plink-1.07-unclobber-i.patch" "plink-endian-detection.patch")))) (build-system gnu-build-system) (arguments `(#:tests? #f ;no "check" target #:make-flags ,#~(list (string-append "LIB_LAPACK=" #$(this-package-input "openblas") "/lib/libopenblas.so") "WITH_LAPACK=1" "FORCE_DYNAMIC=1" ;; disable phoning home "WITH_WEBCHECK=") #:phases (modify-phases %standard-phases ;; no "configure" script (delete 'configure) (replace 'install (lambda* (#:key outputs #:allow-other-keys) (let ((bin (string-append (assoc-ref outputs "out") "/bin/"))) (install-file "plink" bin))))))) (inputs (list zlib openblas)) (native-inputs (list unzip gcc-8)) (home-page "http://pngu.mgh.harvard.edu/~purcell/plink/") (synopsis "Whole genome association analysis toolset") (description "PLINK is a whole genome association analysis toolset, designed to perform a range of basic, large-scale analyses in a computationally efficient manner. The focus of PLINK is purely on analysis of genotype/phenotype data, so there is no support for steps prior to this (e.g. study design and planning, generating genotype or CNV calls from raw data). Through integration with gPLINK and Haploview, there is some support for the subsequent visualization, annotation and storage of results.") ;; Code is released under GPLv2, except for fisher.h, which is under ;; LGPLv2.1+ (license (list license:gpl2 license:lgpl2.1+)))) (define-public plink-ng (package (inherit plink) (name "plink-ng") (version "2.00a3.3") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/chrchang/plink-ng") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "0m8wkyvbgvcr5kzc284w8fbhpxwglh2c1xq0yc3yv00a53gs7rv0")))) (build-system gnu-build-system) (arguments (list #:tests? #false ;TEST_EXTRACT_CHR doesn't produce expected files #:make-flags #~(list "BLASFLAGS=-lopenblas" "NO_SSE42=1" "NO_AVX2=1" "STATIC_ZSTD=" (string-append "CC=" #$(cc-for-target)) (string-append "PREFIX=" #$output) "DESTDIR=") #:phases '(modify-phases %standard-phases (add-after 'unpack 'chdir (lambda _ (chdir "2.0/build_dynamic"))) (delete 'configure) ; no "configure" script (replace 'check (lambda* (#:key tests? inputs #:allow-other-keys) (when tests? (setenv "PATH" (string-append (getcwd) ":" (getenv "PATH"))) (with-directory-excursion "../Tests" (substitute* "run_tests.sh" (("^./run_tests" m) (string-append (which "bash") " " m))) (invoke "bash" "run_tests.sh"))))) (replace 'install (lambda* (#:key outputs #:allow-other-keys) (install-file "plink2" (string-append (assoc-ref outputs "out") "/bin"))))))) (inputs (list openblas zlib `(,zstd "lib"))) (native-inputs (list diffutils plink python simde)) ; for tests (home-page "https://www.cog-genomics.org/plink/") (license license:gpl3+))) (define-public smithlab-cpp (let ((revision "1") (commit "728a097bec88c6f4b8528b685932049e660eff2e")) (package (name "smithlab-cpp") (version (string-append "0." revision "." (string-take commit 7))) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/smithlabcode/smithlab_cpp") (commit commit))) (file-name (string-append name "-" version "-checkout")) (sha256 (base32 "0d476lmj312xk77kr9fzrv7z1bv96yfyx0w7y62ycmnfbx32ll74")))) (build-system gnu-build-system) (arguments `(#:modules ((guix build gnu-build-system) (guix build utils) (srfi srfi-26)) #:tests? #f ;no "check" target #:phases (modify-phases %standard-phases (add-after 'unpack 'use-samtools-headers (lambda _ (substitute* '("SAM.cpp" "SAM.hpp") (("sam.h") "samtools/sam.h")) #t)) (replace 'install (lambda* (#:key outputs #:allow-other-keys) (let* ((out (assoc-ref outputs "out")) (lib (string-append out "/lib")) (include (string-append out "/include/smithlab-cpp"))) (mkdir-p lib) (mkdir-p include) (for-each (cut install-file <> lib) (find-files "." "\\.o$")) (for-each (cut install-file <> include) (find-files "." "\\.hpp$"))) #t)) (delete 'configure)))) (inputs (list samtools-0.1 zlib)) (home-page "https://github.com/smithlabcode/smithlab_cpp") (synopsis "C++ helper library for functions used in Smith lab projects") (description "Smithlab CPP is a C++ library that includes functions used in many of the Smith lab bioinformatics projects, such as a wrapper around Samtools data structures, classes for genomic regions, mapped sequencing reads, etc.") (license license:gpl3+)))) (define-public preseq (package (name "preseq") (version "2.0.3") (source (origin (method url-fetch) (uri (string-append "https://github.com/smithlabcode/preseq/" "releases/download/v" version "/preseq_v" version ".tar.bz2")) (sha256 (base32 "149x9xmk1wy1gff85325yfzqc0qk4sgp1w6gbyj9cnji4x1dszbl")) (modules '((guix build utils))) ;; Remove bundled samtools. (snippet '(delete-file-recursively "samtools")))) (build-system gnu-build-system) (arguments `(#:tests? #f ;no "check" target #:phases (modify-phases %standard-phases (delete 'configure)) #:make-flags ,#~(list (string-append "PREFIX=" #$output) (string-append "LIBBAM=" #$(this-package-input "samtools") "/lib/libbam.a") (string-append "SMITHLAB_CPP=" #$(this-package-input "smithlab-cpp") "/lib") "PROGS=preseq" "INCLUDEDIRS=$(SMITHLAB_CPP)/../include/smithlab-cpp $(SAMTOOLS_DIR)"))) (inputs (list gsl samtools-0.1 smithlab-cpp zlib)) (home-page "http://smithlabresearch.org/software/preseq/") (synopsis "Program for analyzing library complexity") (description "The preseq package is aimed at predicting and estimating the complexity of a genomic sequencing library, equivalent to predicting and estimating the number of redundant reads from a given sequencing depth and how many will be expected from additional sequencing using an initial sequencing experiment. The estimates can then be used to examine the utility of further sequencing, optimize the sequencing depth, or to screen multiple libraries to avoid low complexity samples.") (license license:gpl3+))) (define-public python-screed (package (name "python-screed") (version "1.1.2") (source (origin (method url-fetch) (uri (pypi-uri "screed" version)) (sha256 (base32 "0slva743xn93h4sl5zg2as4ricnnj5pp6nw9dm4qclk4i9xglkvk")))) (build-system pyproject-build-system) (native-inputs (list python-pytest-cov python-pytest-runner)) (home-page "https://github.com/dib-lab/screed/") (synopsis "Short read sequence database utilities") (description "Screed parses FASTA and FASTQ files and generates databases. Values such as sequence name, sequence description, sequence quality and the sequence itself can be retrieved from these databases.") (license license:bsd-3))) (define-public python-slamdunk (package (name "python-slamdunk") (version "0.4.3") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/t-neumann/slamdunk") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "0lv3h5k2pn1pz35kz0wk5xmricxzy8qscs2y7nwh0k6x4pn0m0s5")))) (build-system python-build-system) (propagated-inputs (list python-biopython python-intervaltree python-joblib python-pandas python-pybedtools python-pysam)) (native-inputs (list python-cython python-pytest)) (home-page "https://t-neumann.github.io/slamdunk/") (synopsis "Streamline SLAM-seq analysis with high sensitivity") (description "SlamDunk is a fully automated tool for automated, robust, scalable and reproducible SLAMseq data analysis. Diagnostic plotting features and a MultiQC plugin will make your SLAMseq data ready for immediate QA and interpretation.") (license license:agpl3+))) (define-public python-taggd (package (name "python-taggd") (version "0.3.6") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/SpatialTranscriptomicsResearch/taggd") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "0j19ah81z7aqrdljah9hyarp91gvgbk63pz6fz3pdpksy1yqyi6k")) (modules '((guix build utils))) (snippet '(for-each delete-file (find-files "taggd" "\\.c$"))))) (build-system python-build-system) (arguments (list #:phases '(modify-phases %standard-phases (add-after 'unpack 'disable-broken-tests (lambda _ (substitute* "tests/taggd_demultiplex_test.py" (("def test_normal_bam_run") "def _disabled_test_normal_bam_run"))))))) (propagated-inputs (list python-numpy python-pysam python-setuptools)) (native-inputs (list python-cython)) (home-page "https://github.com/SpatialTranscriptomicsResearch/taggd") (synopsis "Genetic barcode demultiplexing") (description "This package provides TagGD barcode demultiplexing utilities for Spatial Transcriptomics data.") (license license:bsd-3))) (define-public stpipeline (package (name "stpipeline") (version "1.8.1") (source (origin (method url-fetch) (uri (pypi-uri "stpipeline" version)) (sha256 (base32 "0har2g42fvaqpiz66lincy86aj1hvwzds26kxhxfamvyvv4721wk")))) (build-system python-build-system) (arguments (list #:phases '(modify-phases %standard-phases (add-after 'unpack 'relax-requirements (lambda _ (substitute* "requirements.txt" (("argparse.*") ""))))))) (propagated-inputs (list htseq python-cython python-invoke python-numpy python-pandas python-pympler python-pysam python-regex python-scikit-learn python-scipy python-seaborn python-setuptools python-sqlitedict python-taggd samtools star)) (home-page "https://github.com/SpatialTranscriptomicsResearch/st_pipeline") (synopsis "Pipeline for spatial mapping of unique transcripts") (description "This package provides an automated pipeline for spatial mapping of unique transcripts.") (license license:expat))) (define-public sra-tools (package (name "sra-tools") (version "2.10.6") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/ncbi/sra-tools") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "1cr2mijkfs5sm35ffjs6861qsd1qkgnhnbavdv65zg5d655abbjf")))) (build-system gnu-build-system) (arguments (list #:parallel-build? #f ; not supported #:tests? #f ; no "check" target #:make-flags #~(list (string-append "DEFAULT_CRT=" #$(this-package-input "ncbi-vdb") "/kfg/certs.kfg") (string-append "DEFAULT_KFG=" #$(this-package-input "ncbi-vdb") "/kfg/default.kfg") (string-append "VDB_LIBDIR=" #$(this-package-input "ncbi-vdb") #$(if (string-prefix? "x86_64" (or (%current-target-system) (%current-system))) "/lib64" "/lib32"))) #:phases #~(modify-phases %standard-phases (add-before 'configure 'set-perl-search-path (lambda _ ;; Work around "dotless @INC" build failure. (setenv "PERL5LIB" (string-append (getcwd) "/setup:" (getenv "PERL5LIB"))))) (replace 'configure (lambda* (#:key inputs outputs #:allow-other-keys) ;; The build system expects a directory containing the sources and ;; raw build output of ncbi-vdb, including files that are not ;; installed. Since we are building against an installed version of ;; ncbi-vdb, the following modifications are needed. (substitute* "setup/konfigure.perl" ;; Make the configure script look for the "ilib" directory of ;; "ncbi-vdb" without first checking for the existence of a ;; matching library in its "lib" directory. (("^ my \\$f = File::Spec->catdir\$\\$libdir, \\$lib\$;") "my $f = File::Spec->catdir($ilibdir, $ilib);") ;; Look for interface libraries in ncbi-vdb's "ilib" directory. (("my \\$ilibdir = File::Spec->catdir\$\\$builddir, 'ilib'\$;") "my $ilibdir = File::Spec->catdir($dir, 'ilib');")) ;; Dynamic linking (substitute* "tools/copycat/Makefile" (("smagic-static") "lmagic")) (substitute* "tools/driver-tool/utf8proc/Makefile" (("CC\\?=gcc") "myCC=gcc") (("\$CC\$") "(myCC)")) ;; Don't link libxml2 statically (substitute* "build/ld.linux.exe.sh" (("grep -q 'OS_DISTRIBUTOR = Ubuntu.*") "true\n")) ;; The 'configure' script doesn't recognize things like ;; '--enable-fast-install'. (invoke "./configure" (string-append "--build-prefix=" (getcwd) "/build") (string-append "--prefix=" #$output) (string-append "--debug") (string-append "--with-fuse-prefix=" #$(this-package-input "fuse")) (string-append "--with-magic-prefix=" #$(this-package-input "file")) (string-append "--with-xml2-prefix=" #$(this-package-input "libxml2")) (string-append "--with-ncbi-vdb-sources=" #$(this-package-input "ncbi-vdb")) (string-append "--with-ncbi-vdb-build=" #$(this-package-input "ncbi-vdb")) (string-append "--with-ngs-sdk-prefix=" #$(this-package-input "ngs-sdk")) (string-append "--with-hdf5-prefix=" #$(this-package-input "hdf5")))))))) (native-inputs (list perl)) (inputs (list ngs-sdk ncbi-vdb file fuse-2 hdf5-1.10 libxml2 zlib python-wrapper)) (home-page "https://trace.ncbi.nlm.nih.gov/Traces/sra/sra.cgi?view=software") (synopsis "Tools and libraries for reading and writing sequencing data") (description "The SRA Toolkit from NCBI is a collection of tools and libraries for reading of sequencing files from the Sequence Read Archive (SRA) database and writing files into the .sra format.") (license license:public-domain))) (define-public seqan (package (name "seqan") (version "3.0.3") (source (origin (method url-fetch) (uri (string-append "https://github.com/seqan/seqan3/releases/" "download/" version "/seqan3-" version "-Source.tar.xz")) (sha256 (base32 "1h2z0cvgidhkmh5xsbw75waqbrqbbv6kkrvb0b92xfh3gqpaiz22")))) (build-system cmake-build-system) (arguments `(#:phases (modify-phases %standard-phases (replace 'check (lambda _ (invoke "ctest" "test" "--output-on-failure")))))) (native-inputs (list bzip2 cereal zlib)) (home-page "https://www.seqan.de") (synopsis "Library for nucleotide sequence analysis") (description "SeqAn is a C++ library of efficient algorithms and data structures for the analysis of sequences with the focus on biological data. It contains algorithms and data structures for string representation and their manipulation, online and indexed string search, efficient I/O of bioinformatics file formats, sequence alignment, and more.") (license license:bsd-3))) (define-public seqan-2 (package (inherit seqan) (version "2.4.0") (source (origin (method url-fetch) (uri (string-append "https://github.com/seqan/seqan/releases/" "download/seqan-v" version "/seqan-library-" version ".tar.xz")) (sha256 (base32 "19a1rlxx03qy1i1iriicly68w64yjxbv24g9gdywnfmq998v35yx")))) ;; The documentation is 7.8MB and the includes are 3.6MB heavy, so it ;; makes sense to split the outputs. (outputs '("out" "doc")) (build-system trivial-build-system) (arguments `(#:modules ((guix build utils)) #:builder ,#~(begin (use-modules (guix build utils)) (let ((tar #$(this-package-native-input "tar")) (xz #$(this-package-native-input "xz")) (out #$output) (doc #$output:doc)) (setenv "PATH" (string-append tar "/bin:" xz "/bin")) (invoke "tar" "xvf" #$(this-package-native-input "source")) (chdir (string-append "seqan-library-" #$version)) (copy-recursively "include" (string-append out "/include")) (copy-recursively "share" (string-append doc "/share")))))) (native-inputs `(("source" ,source) ("tar" ,tar) ("xz" ,xz))))) (define-public seqan-1 (package (inherit seqan) (name "seqan") (version "1.4.2") (source (origin (method url-fetch) (uri (string-append "https://packages.seqan.de/seqan-library/" "seqan-library-" version ".tar.bz2")) (sha256 (base32 "05s3wrrwn50f81aklfm65i4a749zag1vr8z03k21xm0pdxy47yvp")))) ;; The documentation is 7.8MB and the includes are 3.6MB heavy, so it ;; makes sense to split the outputs. (outputs '("out" "doc")) (build-system trivial-build-system) (arguments `(#:modules ((guix build utils)) #:builder ,#~(begin (use-modules (guix build utils)) (let ((tar #$(this-package-native-input "tar")) (bzip #$(this-package-native-input "bzip2")) (out #$output) (doc #$output:doc)) (setenv "PATH" (string-append tar "/bin:" bzip "/bin")) (invoke "tar" "xvf" #$(this-package-native-input "source")) (chdir (string-append "seqan-library-" #$version)) (copy-recursively "include" (string-append out "/include")) (copy-recursively "share" (string-append doc "/share")))))) (native-inputs `(("source" ,source) ("tar" ,tar) ("bzip2" ,bzip2))))) (define-public seqmagick (package (name "seqmagick") (version "0.8.4") (source (origin (method url-fetch) (uri (pypi-uri "seqmagick" version)) (sha256 (base32 "0c6skyig8fyylnbj4597pjj9h0dn36rkxrhwd34yrsc6k6f7r8a0")))) (build-system pyproject-build-system) (inputs (list python-biopython python-pygtrie)) (native-inputs (list python-pytest)) (home-page "https://github.com/fhcrc/seqmagick") (synopsis "Tools for converting and modifying sequence files") (description "Bioinformaticians often have to convert sequence files between formats and do little manipulations on them, and it's not worth writing scripts for that. Seqmagick is a utility to expose the file format conversion in BioPython in a convenient way. Instead of having a big mess of scripts, there is one that takes arguments.") (license license:gpl3))) (define-public seqtk (package (name "seqtk") (version "1.3") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/lh3/seqtk") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "1bfzlqa84b5s1qi22blmmw2s8xdyp9h9ydcq22pfjhh5gab3yz6l")))) (build-system gnu-build-system) (arguments `(#:phases (modify-phases %standard-phases (delete 'configure) (replace 'check ;; There are no tests, so we just run a sanity check. (lambda _ (invoke "./seqtk" "seq") #t)) (replace 'install (lambda* (#:key outputs #:allow-other-keys) (let ((bin (string-append (assoc-ref outputs "out") "/bin/"))) (install-file "seqtk" bin) #t)))))) (inputs (list zlib)) (home-page "https://github.com/lh3/seqtk") (synopsis "Toolkit for processing biological sequences in FASTA/Q format") (description "Seqtk is a fast and lightweight tool for processing sequences in the FASTA or FASTQ format. It parses both FASTA and FASTQ files which can be optionally compressed by gzip.") (license license:expat))) (define-public snap-aligner (package (name "snap-aligner") (version "2.0.0") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/amplab/snap") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "0yag3jcazdqfxgmw0vbi91i98kj9sr0aqx83qqj6m5b45wxs7jms")))) (build-system gnu-build-system) (arguments '(#:phases (modify-phases %standard-phases (delete 'configure) (replace 'check (lambda* (#:key tests? #:allow-other-keys) (when tests? (invoke "./unit_tests")))) (replace 'install (lambda* (#:key outputs #:allow-other-keys) (let* ((out (assoc-ref outputs "out")) (bin (string-append out "/bin"))) (install-file "snap-aligner" bin) (install-file "SNAPCommand" bin))))))) (native-inputs (list zlib)) (home-page "https://snap.cs.berkeley.edu/") (synopsis "Short read DNA sequence aligner") (description "SNAP is a fast and accurate aligner for short DNA reads. It is optimized for modern read lengths of 100 bases or higher, and takes advantage of these reads to align data quickly through a hash-based indexing scheme.") ;; 32-bit systems are not supported by the unpatched code. ;; Following the bug reports https://github.com/amplab/snap/issues/68 and ;; https://bugs.debian.org/cgi-bin/bugreport.cgi?bug=812378 we see that ;; systems without a lot of memory cannot make good use of this program. (supported-systems '("x86_64-linux")) (license license:asl2.0))) (define-public sortmerna (package (name "sortmerna") (version "4.3.4") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/biocore/sortmerna") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "0f8jfc8vsq6llhbb92p9yv7nbp566yqwfcmq3g2hw0n7d8hyl3a8")))) (build-system cmake-build-system) (outputs '("out" ;for binaries "db")) ;for sequence databases (arguments (list #:tests? #false ;unclear how to run them #:configure-flags #~(list "-DWITH_TESTS=ON" "-DCMAKE_CXX_FLAGS=-pthread" "-DZLIB_STATIC=OFF" "-DROCKSDB_STATIC=OFF" "-DPORTABLE=OFF" ;do not use static linking (string-append "-DROCKSDB_HOME=" #$(this-package-input "rocksdb")) (string-append "-DRAPIDJSON_HOME=" #$(this-package-input "rapidjson")) (string-append "-DRapidJson_DIR=" #$(this-package-input "rapidjson") "/lib/cmake/RapidJSON") (string-append "-DRapidJSON_INCLUDE_DIR=" #$(this-package-input "rapidjson") "/include")) #:phases '(modify-phases %standard-phases (add-after 'unpack 'find-concurrentqueue-headers (lambda* (#:key inputs #:allow-other-keys) ;; Ensure that headers can be found (setenv "CPLUS_INCLUDE_PATH" (string-append (search-input-directory inputs "/include/concurrentqueue") ":" (or (getenv "CPLUS_INCLUDE_PATH") ""))))) (replace 'install (lambda* (#:key outputs #:allow-other-keys) (let* ((out (assoc-ref outputs "out")) (bin (string-append out "/bin")) (db (assoc-ref outputs "db")) (share (string-append db "/share/sortmerna/rRNA_databases"))) (install-file "src/sortmerna" bin) (for-each (lambda (file) (install-file file share)) (find-files "../source/data/rRNA_databases" ".*fasta")))))))) (inputs (list concurrentqueue gflags ; because of rocksdb rapidjson rocksdb zlib)) (native-inputs (list pkg-config)) (home-page "https://bioinfo.lifl.fr/RNA/sortmerna/") (synopsis "Biological sequence analysis tool for NGS reads") (description "SortMeRNA is a biological sequence analysis tool for filtering, mapping and @acronym{OTU, operational taxonomic unit} picking of @acronym{NGS, next generation sequencing} reads. The core algorithm is based on approximate seeds and allows for fast and sensitive analyses of nucleotide sequences. The main application of SortMeRNA is filtering rRNA from metatranscriptomic data.") ;; The source includes x86 specific code (supported-systems '("x86_64-linux" "i686-linux")) (license license:lgpl3))) (define-public star (package (name "star") (version "2.7.8a") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/alexdobin/STAR") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "0zc5biymja9zml9yizcj1h68fq9c6sxfcav8a0lbgvgsm44rvans")) (modules '((guix build utils))) (snippet '(begin (substitute* "source/Makefile" (("/bin/rm") "rm")) ;; Remove pre-built binaries and bundled htslib sources. (delete-file-recursively "bin/MacOSX_x86_64") (delete-file-recursively "bin/Linux_x86_64") (delete-file-recursively "bin/Linux_x86_64_static") (delete-file-recursively "source/htslib") #t)))) (build-system gnu-build-system) (arguments '(#:tests? #f ;no check target #:make-flags '("STAR") #:phases (modify-phases %standard-phases (add-after 'unpack 'enter-source-dir (lambda _ (chdir "source") #t)) (add-after 'enter-source-dir 'make-reproducible (lambda _ (substitute* "Makefile" (("(COMPILATION_TIME_PLACE=\")(.*)(\")" _ pre mid post) (string-append pre "Built with Guix" post))) #t)) ;; See https://github.com/alexdobin/STAR/pull/562 (add-after 'enter-source-dir 'add-missing-header (lambda _ (substitute* "SoloReadFeature_inputRecords.cpp" (("#include \"binarySearch2.h\"" h) (string-append h "\n#include <math.h>"))) #t)) (add-after 'enter-source-dir 'do-not-use-bundled-htslib (lambda _ (substitute* "Makefile" (("(Depend.list: \\$\$SOURCES\$ parametersDefault\\.xxd) htslib" _ prefix) prefix)) (substitute* '("BAMfunctions.cpp" "signalFromBAM.h" "bam_cat.h" "bam_cat.c" "STAR.cpp" "bamRemoveDuplicates.cpp") (("#include \"htslib/([^\"]+\\.h)\"" _ header) (string-append "#include <" header ">"))) (substitute* "IncludeDefine.h" (("\"htslib/(htslib/[^\"]+.h)\"" _ header) (string-append "<" header ">"))) #t)) (replace 'install (lambda* (#:key outputs #:allow-other-keys) (let ((bin (string-append (assoc-ref outputs "out") "/bin/"))) (install-file "STAR" bin)) #t)) (delete 'configure)))) (native-inputs (list xxd)) (inputs (list htslib zlib)) (home-page "https://github.com/alexdobin/STAR") (synopsis "Universal RNA-seq aligner") (description "The Spliced Transcripts Alignment to a Reference (STAR) software is based on a previously undescribed RNA-seq alignment algorithm that uses sequential maximum mappable seed search in uncompressed suffix arrays followed by seed clustering and stitching procedure. In addition to unbiased de novo detection of canonical junctions, STAR can discover non-canonical splices and chimeric (fusion) transcripts, and is also capable of mapping full-length RNA sequences.") ;; Only 64-bit systems are supported according to the README. (supported-systems '("x86_64-linux" "mips64el-linux")) ;; STAR is licensed under GPLv3 or later; htslib is MIT-licensed. (license license:gpl3+))) (define-public star-for-pigx (package (inherit star) (name "star") (version "2.7.3a") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/alexdobin/STAR") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "1hgiqw5qhs0pc1xazzihcfd92na02xyq2kb469z04y1v51kpvvjq")) (modules '((guix build utils))) (snippet '(begin (substitute* "source/Makefile" (("/bin/rm") "rm")) ;; Remove pre-built binaries and bundled htslib sources. (delete-file-recursively "bin/MacOSX_x86_64") (delete-file-recursively "bin/Linux_x86_64") (delete-file-recursively "bin/Linux_x86_64_static") (delete-file-recursively "source/htslib") #t)))))) (define-public starlong (package (inherit star) (name "starlong") (arguments (substitute-keyword-arguments (package-arguments star) ((#:make-flags flags) `(list "STARlong")) ((#:phases phases) `(modify-phases ,phases ;; Allow extra long sequence reads. (add-after 'unpack 'make-extra-long (lambda _ (substitute* "source/IncludeDefine.h" (("(#define DEF_readNameLengthMax ).*" _ match) (string-append match "900000\n"))) #t)) (replace 'install (lambda* (#:key outputs #:allow-other-keys) (let ((bin (string-append (assoc-ref outputs "out") "/bin/"))) (install-file "STARlong" bin)) #t)))))))) (define-public subread (package (name "subread") (version "2.0.3") (source (origin (method url-fetch) (uri (string-append "mirror://sourceforge/subread/subread-" version "/subread-" version "-source.tar.gz")) (sha256 (base32 "0szmllia7jl0annk5568xjhw6cc8yj1c5mb961qk5m0lz6ig7kjn")))) (build-system gnu-build-system) (arguments `(#:tests? #f ;no "check" target ;; The CC and CCFLAGS variables are set to contain a lot of x86_64 ;; optimizations by default, so we override these flags such that x86_64 ;; flags are only added when the build target is an x86_64 system. #:make-flags (list (let ((system ,(or (%current-target-system) (%current-system))) (flags '("-ggdb" "-fomit-frame-pointer" "-ffast-math" "-funroll-loops" "-fmessage-length=0" "-fcommon" "-O9" "-Wall" "-DMAKE_FOR_EXON" "-DMAKE_STANDALONE" "-DSUBREAD_VERSION=\\\"${SUBREAD_VERSION}\\\"")) (flags64 '("-mmmx" "-msse" "-msse2" "-msse3"))) (if (string-prefix? "x86_64" system) (string-append "CCFLAGS=" (string-join (append flags flags64))) (string-append "CCFLAGS=" (string-join flags)))) "-f" "Makefile.Linux" "CC=gcc ${CCFLAGS}") #:phases (modify-phases %standard-phases (add-after 'unpack 'enter-dir (lambda _ (chdir "src"))) (replace 'install (lambda* (#:key outputs #:allow-other-keys) (let ((bin (string-append (assoc-ref outputs "out") "/bin/"))) (mkdir-p bin) (copy-recursively "../bin" bin)))) ;; no "configure" script (delete 'configure)))) (inputs (list zlib)) (home-page "https://subread.sourceforge.net/") (synopsis "Tool kit for processing next-gen sequencing data") (description "The subread package contains the following tools: subread aligner, a general-purpose read aligner; subjunc aligner: detecting exon-exon junctions and mapping RNA-seq reads; featureCounts: counting mapped reads for genomic features; exactSNP: a SNP caller that discovers SNPs by testing signals against local background noises.") (license license:gpl3+))) (define-public stringtie (package (name "stringtie") (version "2.2.0") (source (origin (method url-fetch) (uri (string-append "http://ccb.jhu.edu/software/stringtie/dl/" "stringtie-" version ".tar.gz")) (sha256 (base32 "08w3ish4y9kf9acp7k38iwi8ixa6j51m6qyf0vvfj7yz78a3ai3x")) ;; This package bundles an annoying amount of third party source ;; code. (modules '((guix build utils))) (snippet '(delete-file-recursively "htslib")))) (build-system gnu-build-system) (arguments `(#:tests? #f ;no test suite #:make-flags '("LIBDEFLATE=-ldeflate" "LIBBZ2=-lbz2" "LIBLZMA=-llzma") #:phases (modify-phases %standard-phases ;; no configure script (delete 'configure) (add-before 'build 'use-system-samtools (lambda _ (substitute* "Makefile" ((" -lm") " -lm -lhts") ((" \\$\\{HTSLIB\\}/libhts\\.a") " ")))) (replace 'install (lambda* (#:key outputs #:allow-other-keys) (let ((bin (string-append (assoc-ref outputs "out") "/bin/"))) (install-file "stringtie" bin))))))) (inputs (list bzip2 htslib-for-stringtie libdeflate zlib)) (home-page "https://ccb.jhu.edu/software/stringtie/") (synopsis "Transcript assembly and quantification for RNA-Seq data") (description "StringTie is a fast and efficient assembler of RNA-Seq sequence alignments into potential transcripts. It uses a novel network flow algorithm as well as an optional de novo assembly step to assemble and quantitate full-length transcripts representing multiple splice variants for each gene locus. Its input can include not only the alignments of raw reads used by other transcript assemblers, but also alignments of longer sequences that have been assembled from those reads. To identify differentially expressed genes between experiments, StringTie's output can be processed either by the Cuffdiff or Ballgown programs.") (license license:expat))) (define-public taxtastic (package (name "taxtastic") (version "0.9.2") (source (origin ;; The Pypi version does not include tests. (method git-fetch) (uri (git-reference (url "https://github.com/fhcrc/taxtastic") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "1k6wg9ych1j3srnhdny1y4470qlhfg730rb3rm3pq7l7gw62vmgb")))) (build-system python-build-system) (arguments `(#:phases (modify-phases %standard-phases (add-after 'unpack 'prepare-directory (lambda _ ;; This test fails, but the error is not caught by the test ;; framework, so the tests fail... (substitute* "tests/test_taxit.py" (("self.cmd_fails\$''\$") "self.cmd_fails('nothing')")) ;; This version file is expected to be created with git describe. (mkdir-p "taxtastic/data") (with-output-to-file "taxtastic/data/ver" (lambda () (display ,version))))) (replace 'check ;; Note, this fails to run with "-v" as it tries to write to a ;; closed output stream. (lambda* (#:key tests? #:allow-other-keys) (when tests? (invoke "python" "-m" "unittest")))) ;; This fails because it cannot find psycopg2 even though it is ;; available. (delete 'sanity-check)))) (propagated-inputs (list python-sqlalchemy python-decorator python-biopython python-pandas python-psycopg2 python-fastalite python-pyyaml python-six python-jinja2 python-dendropy)) (home-page "https://github.com/fhcrc/taxtastic") (synopsis "Tools for taxonomic naming and annotation") (description "Taxtastic is software written in python used to build and maintain reference packages i.e. collections of reference trees, reference alignments, profiles, and associated taxonomic information.") (license license:gpl3+))) (define-public vcftools (package (name "vcftools") (version "0.1.16") (source (origin (method url-fetch) (uri (string-append "https://github.com/vcftools/vcftools/releases/download/v" version "/vcftools-" version ".tar.gz")) (sha256 (base32 "1qqlx7flfv7axrjwkaz6njkscsl1d0jw98ns8d8bh1n1hd1pgz6v")))) (build-system gnu-build-system) (arguments `(#:tests? #f ; no "check" target #:make-flags ,#~(list "CFLAGS=-O2" ; override "-m64" flag (string-append "PREFIX=" #$output) (string-append "MANDIR=" #$output "/share/man/man1")))) (native-inputs (list pkg-config)) (inputs (list perl zlib)) (home-page "https://vcftools.github.io/") (synopsis "Tools for working with VCF files") (description "VCFtools is a program package designed for working with VCF files, such as those generated by the 1000 Genomes Project. The aim of VCFtools is to provide easily accessible methods for working with complex genetic variation data in the form of VCF files.") ;; The license is declared as LGPLv3 in the README and ;; at https://vcftools.github.io/license.html (license license:lgpl3))) (define-public infernal (package (name "infernal") (version "1.1.4") (source (origin (method url-fetch) (uri (string-append "http://eddylab.org/software/infernal/" "infernal-" version ".tar.gz")) (sha256 (base32 "1z4mgwqg1j4n5ika08ai8mg9yjyjhf4821jp83v2bgwzxrykqjgr")))) (build-system gnu-build-system) (native-inputs (list perl python)) ; for tests (home-page "http://eddylab.org/infernal/") (synopsis "Inference of RNA alignments") (description "Infernal (\"INFERence of RNA ALignment\") is a tool for searching DNA sequence databases for RNA structure and sequence similarities. It is an implementation of a special case of profile stochastic context-free grammars called @dfn{covariance models} (CMs). A CM is like a sequence profile, but it scores a combination of sequence consensus and RNA secondary structure consensus, so in many cases, it is more capable of identifying RNA homologs that conserve their secondary structure more than their primary sequence.") ;; Infernal 1.1.3 requires VMX or SSE capability for parallel instructions. (supported-systems '("i686-linux" "x86_64-linux")) (license license:bsd-3))) (define-public r-ggexpress (let ((commit "82f169385f87af328ff971195c2f64ff3c573a8a") (revision "1")) (package (name "r-ggexpress") (version (git-version "0.6.6" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/vertesy/ggExpress") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "122hnw8xv33ngcd4fd7hmf817a06ih1knrxxi0cgklj1fwinm0z4")))) (properties `((upstream-name . "ggExpress"))) (build-system r-build-system) (propagated-inputs (list r-cowplot r-ggplot2 r-ggpubr r-markdownhelpers r-markdownreports r-rcolorbrewer r-sessioninfo r-seurat r-sm r-stringendo r-tidyverse)) (home-page "https://github.com/vertesy/ggExpress") (synopsis "This is a fast tool to create, annotate and export plots in R") (description "This package is a set of R functions for generating precise figures. This tool helps you to create clean markdown reports about what you just discovered with your analysis script.") (license license:gpl3)))) (define-public r-gg3d (let ((commit "ffdd837d30c1671cd0895db94bdd7b1594dbfcb0") (revision "1")) (package (name "r-gg3d") (version (git-version "0.0.0.9000" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/AckerDWM/gg3D") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0vz5laj5vz9m1jzb7h7q9f37zjmxwhylhaidlsg61r57wpxvjr3p")))) (properties `((upstream-name . "gg3D"))) (build-system r-build-system) (propagated-inputs (list r-dplyr r-ggplot2 r-magrittr r-plot3d r-plyr r-scales)) (native-inputs (list r-knitr)) (home-page "https://github.com/AckerDWM/gg3D") (synopsis "3D perspective plots for ggplot2") (description "This package adds 3D perspective plotting of points, paths, and line, 3D perspective axes, 3D perspective annotations, and wireframe plots.") (license license:gpl3+)))) (define-public r-ggsankey (let ((commit "be08dd0f86eaee9f9ff9e7ff95d47930660a3c36") (revision "1")) (package (name "r-ggsankey") (version (git-version "0.0.99999" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/davidsjoberg/ggsankey") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0acpmydqqc91pq5p9wpkpmgqp3nhiljabd7d3i00kwhjxgm2bvba")))) (properties `((upstream-name . "ggsankey"))) (build-system r-build-system) (propagated-inputs (list r-dplyr r-ggplot2 r-magrittr r-purrr r-stringr r-tidyr)) (home-page "https://github.com/davidsjoberg/ggsankey") (synopsis "Sankey, Alluvial and Sankey bump plots") (description "This package provides a package that makes it easy to implement sankey, alluvial and sankey bump plots in @code{ggplot2}.") (license license:expat)))) (define-public r-gutils (let ((commit "10e36c7b580aacb2d952140a3fdd82418aaddea6") (revision "1")) (package (name "r-gutils") (version (git-version "0.2.0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/mskilab/gUtils") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "1wq9kd1afzy7ii510r20c4n9fkykj6p15q5c85ws27h1q5w4ghxy")))) (properties `((upstream-name . "gUtils"))) (build-system r-build-system) (propagated-inputs (list r-biocgenerics r-data-table r-genomeinfodb r-genomicranges r-iranges r-matrix r-s4vectors r-stringr)) (home-page "https://github.com/mskilab/gUtils") (synopsis "Additional capabilities and speed for GenomicRanges operations") (description "This is an R package providing additional capabilities and speed for @code{GenomicRanges} operations.") (license license:gpl2)))) (define-public r-bamutils (let ((commit "639dba901f16944fa1b7a8d7048701ba86a2cdb8") (revision "1")) (package (name "r-bamutils") (version (git-version "0.0.0.9000" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/mskilab/bamutils/") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0qwby2v5rydnipvf1iv1wz9nf02yq98k0xbc4inf9mqc54jwacs0")))) (properties `((upstream-name . "bamUtils"))) (build-system r-build-system) (propagated-inputs (list r-abind r-biocgenerics r-data-table r-genomicalignments r-genomicranges r-gutils r-rsamtools r-variantannotation)) (home-page "https://github.com/mskilab/bamutils/") (synopsis "Utility functions for manipulating BAMs") (description "This package provides utility functions for manipulating BAM files.") (license license:gpl2)))) (define-public r-gtrack (let ((commit "a694fa36cedafca2658da79fc8e5b673535b15e5") (revision "1")) (package (name "r-gtrack") (version (git-version "0.1.0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/mskilab/gTrack/") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "070qlrbqsbj9max2vx740zigqh0ymvnw2pm1ia5la3wb4dbfwh2b")))) (properties `((upstream-name . "gTrack"))) (build-system r-build-system) (propagated-inputs (list r-biocgenerics r-data-table r-genomeinfodb r-genomicranges r-gutils r-iranges r-matrix r-rcolorbrewer r-rcpp r-rcurl r-rtracklayer r-s4vectors)) (home-page "https://github.com/mskilab/gTrack/") (synopsis "Plot tracks of complex genomic data across multiple genomic windows") (description "This package provides an object for plotting GRanges, RleList, UCSC file formats, and ffTrack objects in multi-track panels.") (license license:gpl2)))) (define-public r-gchain (let ((commit "dc393e8dd0d8efaf36270c04d7112db8553db36a") (revision "1")) (package (name "r-gchain") (version (git-version "0.2.0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/mskilab/gChain/") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "105wgi5w2fhwq1grsvj6zjigwg0sny3z7zr577q8ki3qffjwdkj0")))) (properties `((upstream-name . "gChain"))) (build-system r-build-system) (propagated-inputs (list r-bamutils r-biostrings r-data-table r-genomicalignments r-genomicranges r-gtrack r-gutils r-matrix r-rtracklayer)) (home-page "https://github.com/mskilab/gChain/") (synopsis "Additional capabilities and speed for GenomicRanges operations") (description "This R package provides additional capabilities and speed for GenomicRanges operations.") (license license:gpl2)))) (define-public r-skitools (let ((commit "22d107d32f063eb891eb5e7fb36996d1c0b0d2bc") (revision "1")) (package (name "r-skitools") (version (git-version "0.0.0.9000" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/mskilab/skitools/") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "1977d9bkdk9l2n6niahfj9vksh9l1ga4g7c3b3x27lj1gc0qgr4z")))) (properties `((upstream-name . "skitools"))) (build-system r-build-system) (propagated-inputs (list r-biostrings r-complexheatmap r-data-table r-devtools r-dt r-gchain r-genomeinfodb r-genomicranges r-ggplot2 r-gplots r-gutils r-htmlwidgets r-hwriter r-igraph r-iranges r-plotly r-rcolorbrewer r-reshape2 r-s4vectors r-stringr r-variantannotation)) (home-page "https://github.com/mskilab/skitools/") (synopsis "Various mskilab R utilities") (description "This package provides R miscellaneous utilities for basic data manipulation, debugging, visualization, lsf management, and common mskilab tasks.") (license license:expat)))) (define-public r-chromunity (let ((commit "712e56ccba64e8881dbb203546379a5c3c639bb2") (revision "1")) (package (name "r-chromunity") (version (git-version "0.0.2" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/mskilab/chromunity") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0sdja11l7bg5rmcbp2cl226cq9qrj3r8kq5lg49zbin83hya27vh")))) (properties `((upstream-name . "chromunity"))) (build-system r-build-system) (propagated-inputs (list r-arrow r-biocgenerics r-bsgenome-hsapiens-ucsc-hg38 r-data-table r-gchain r-genomicranges r-gutils r-igraph r-magrittr r-mass r-matrix r-pbmcapply r-plyr r-r6 r-zoo)) (home-page "https://github.com/mskilab/chromunity") (synopsis "Discovery of communities in Pore-C concatemers") (description "This is a package for the discovery of communities in Pore-C concatemers.") (license license:gpl3)))) (define-public r-cmdstanr (let ((commit "a45d4f7d686aa6b57ce25f342a71eea79507f01c") (revision "1")) (package (name "r-cmdstanr") (version (git-version "0.8.1.9000" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/stan-dev/cmdstanr") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "01vyh3sy704rs7yvaka2hp6vld0mdl7hbrs20dpbwidgm4ksrvsi")))) (properties `((upstream-name . "cmdstanr"))) (build-system r-build-system) (propagated-inputs (list r-checkmate r-data-table r-jsonlite r-posterior r-processx r-r6 r-rlang r-withr)) (native-inputs (list r-knitr)) (home-page "https://github.com/stan-dev/cmdstanr") (synopsis "R interface to 'CmdStan'") (description "This package provides a lightweight interface to Stan <https://mc-stan.org>. The @code{CmdStanR} interface is an alternative to RStan that calls the command line interface for compilation and running algorithms instead of interfacing with C++ via Rcpp'.") (license license:bsd-3)))) (define-public r-dnamcrosshyb ;; There aren't any releases. (let ((commit "fe8acb33667e81f00dcb84e0fa75c87ab2db5d8f") (revision "1")) (package (name "r-dnamcrosshyb") (version (git-version "0.0.0.9000" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/pjhop/DNAmCrosshyb") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "12j1xsiqpvny5rp23z1az0k4cj5ajbcwkg65z00s16vywi2rx6nb")))) (properties `((upstream-name . "DNAmCrosshyb"))) (build-system r-build-system) (propagated-inputs (list r-biocgenerics r-biocparallel r-biostrings r-bsgenome-hsapiens-ucsc-hg19-masked r-bsgenome-hsapiens-ucsc-hg38-masked r-dplyr r-genomicranges r-ggplot2 r-iranges r-magrittr r-minfi r-purrr r-s4vectors r-shiny r-stringi r-stringr r-tibble r-tidyr r-watermelon)) (home-page "https://github.com/pjhop/DNAmCrosshyb") (synopsis "DNAmCrosshyb") (description "This package provides helper functions to detect cross-hybridization on Illumina DNAm arrays.") (license license:gpl3)))) (define-public r-doubletcollection (let ((commit "c0d62f1853942ee6a087eaf7b000d9e4261e2dfd") (revision "1")) (package (name "r-doubletcollection") (version (git-version "1.1.0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/xnnba1984/DoubletCollection") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "02cvibyc2nwc4037ramm5cskjwyrb9ib9hkrfhmvhbslkn5ixz1v")))) (properties `((upstream-name . "DoubletCollection"))) (build-system r-build-system) (propagated-inputs (list r-biocgenerics r-doubletfinder r-gam r-ggplot2 r-ggthemes r-mast r-mclust r-prroc r-reticulate r-scales r-scdblfinder r-scds r-seurat r-singlecellexperiment r-slingshot r-summarizedexperiment python python-scrublet python-doubletdetection)) (home-page "https://github.com/xnnba1984/DoubletCollection") (synopsis "Tool for finding doublets in scRNA-seq data") (description "This is an R package that integrates the installation of doublet-detection methods. In addition, this tool is used for execution and benchmark of those eight mentioned methods.") (license license:gpl3+)))) (define-public r-plsdabatch (let ((commit "4aadf3a99709afae462db310386b6cf5db20088c") (revision "1")) (package (name "r-plsdabatch") (version (git-version "0.2.3" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/EvaYiwenWang/PLSDAbatch") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "047l923lq2ji7rwybh9b9zkblzvvhkpli5gb2x8g2q9f2n5022nr")))) (properties `((upstream-name . "PLSDAbatch"))) (build-system r-build-system) (propagated-inputs (list r-ggplot2 r-ggpubr r-gridextra r-lmertest r-mixomics r-mvtnorm r-performance r-rdpack r-scales)) (native-inputs (list r-knitr)) (home-page "https://github.com/EvaYiwenWang/PLSDAbatch") (synopsis "PLSDA-batch") (description "This package provides a new batch effect correction method based on Projection to Latent Structures Discriminant Analysis named “PLSDA-batch” to correct data prior to any downstream analysis. PLSDA-batch estimates latent components related to treatment and batch effects to remove batch variation. The method is multivariate, non-parametric and performs dimension reduction. Combined with centered log ratio transformation for addressing uneven library sizes and compositional structure, PLSDA-batch addresses all characteristics of microbiome data that existing correction methods have ignored so far.") (license license:gpl3)))) (define-public r-psupertime (let ((commit "73825a28d3bd9bc881c15ee0c4c218eec1c9c207") (revision "1")) (package (name "r-psupertime") (version (git-version "0.2.6" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/wmacnair/psupertime") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "00h1r3ffz6m9dwcgkvyki8405b059qn6mnjsd8d76a1rabaf2vfh")))) (properties `((upstream-name . "psupertime"))) (build-system r-build-system) (propagated-inputs (list r-cowplot r-data-table r-fastcluster r-forcats r-ggplot2 r-glmnet r-knitr r-matrix r-rcolorbrewer r-scales r-scran r-singlecellexperiment r-stringr r-summarizedexperiment r-topgo)) (native-inputs (list r-knitr)) (home-page "https://github.com/wmacnair/psupertime") (synopsis "Psupertime is supervised pseudotime for single cell RNAseq data") (description "Psupertime is supervised pseudotime for single cell RNAseq data. It uses single cell RNAseq data, where the cells have a known ordering. This ordering helps to identify a small number of genes which place cells in that known order. It can be used for discovery of relevant genes, for identification of subpopulations, and characterization of further unknown or differently labelled data.") (license license:gpl3)))) (define-public r-pando (package (name "r-pando") (version "1.0.5") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/quadbiolab/Pando") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "04kr1b28p5j7h48g32cldkg87xcmxnmd4kspygkfs7a4amihpi66")))) (properties `((upstream-name . "Pando"))) (build-system r-build-system) (arguments (list #:phases '(modify-phases %standard-phases (add-after 'unpack 'loosen-requirements (lambda _ (substitute* "DESCRIPTION" ((" \\(==.*,") ","))))))) (propagated-inputs (list r-bayestestr r-foreach r-genomicranges r-ggplot2 r-ggpointdensity r-ggraph r-glmnetutils r-grr r-iranges r-irlba r-matrix r-matrixgenerics r-motifmatchr r-pals r-patchwork r-seurat r-signac r-sparsematrixstats r-tfbstools r-tidygraph r-tidyverse r-uwot)) (native-inputs (list r-knitr)) (home-page "https://github.com/quadbiolab/Pando") (synopsis "Infer regulomes from multi-modal single-cell genomics data") (description "Pando leverages multi-modal single-cell measurements to infer gene regulatory networks using a flexible linear model-based framework. By modeling the relationship between TF-binding site pairs with the expression of target genes, Pando simultaneously infers gene modules and sets of regulatory regions for each transcription factor.") (license license:expat))) (define-public r-premessa (let ((commit "68b42bb984637d0f3ad6a0ecc83e9278994afc85") (revision "1")) (package (name "r-premessa") (version (git-version "0.3.4" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/ParkerICI/premessa") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "1l0q431zk0lvg22130nx84gdqi7cpl05yah4am63lbx6m4c769pb")) (snippet '(delete-file "inst/normalizer_shinyGUI/www/d3.min.js")))) (properties `((upstream-name . "premessa"))) (build-system r-build-system) (arguments (list #:phases '(modify-phases %standard-phases (add-after 'unpack 'process-javascript (lambda* (#:key inputs #:allow-other-keys) (with-directory-excursion "inst/normalizer_shinyGUI/www/" (invoke "esbuild" (assoc-ref inputs "d3.v4.js") "--minify" "--outfile=d3.min.js"))))))) (propagated-inputs (list r-data-table r-flowcore r-ggplot2 r-gridextra r-hexbin r-jsonlite r-reshape r-rhandsontable r-shiny r-shinyjqui)) (native-inputs `(("esbuild" ,esbuild) ("d3.v4.js" ,(origin (method url-fetch) (uri "https://d3js.org/d3.v4.js") (sha256 (base32 "0y7byf6kcinfz9ac59jxc4v6kppdazmnyqfav0dm4h550fzfqqlg")))))) (home-page "https://github.com/ParkerICI/premessa") (synopsis "Pre-processing of flow and mass cytometry data") (description "This is an R package for pre-processing of flow and mass cytometry data. This package includes panel editing or renaming for FCS files, bead-based normalization and debarcoding.") (license license:gpl3)))) (define-public r-projectils (let ((commit "cc73b97471b4b6eea11ce779b5c4a7dc5c3e1709") (revision "1")) (package (name "r-projectils") (version (git-version "3.0.0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/carmonalab/ProjecTILs") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0dpzvbhhb9andnj7angpj32cgkwd6rs6qgpl6i21pqzcn6vqqhqw")))) (properties `((upstream-name . "ProjecTILs"))) (build-system r-build-system) (propagated-inputs (list r-biocneighbors r-biocparallel r-dplyr r-ggplot2 r-matrix r-patchwork r-pheatmap r-pracma r-purrr r-rcolorbrewer r-reshape2 r-scales r-scgate r-seurat r-seuratobject r-stacas r-ucell r-umap r-uwot)) (home-page "https://github.com/carmonalab/ProjecTILs") (synopsis "Reference-based analysis of scRNA-seq data") (description "This package implements methods to project single-cell RNA-seq data onto a reference atlas, enabling interpretation of unknown cell transcriptomic states in the the context of known, reference states.") (license license:gpl3)))) (define-public r-presto (let ((commit "052085db9c88aa70a28d11cc58ebc807999bf0ad") (revision "0")) (package (name "r-presto") (version (git-version "1.0.0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/immunogenomics/presto") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "1c3fmag4r4p2lvbvxlxyck9dvfw1prbwcl9665mmlx4a35750hk8")))) (properties `((upstream . "presto"))) (build-system r-build-system) (propagated-inputs (list r-data-table r-deseq2 r-dplyr r-matrix r-rcpp r-rcpparmadillo r-reshape2 r-rlang r-tidyr)) (home-page "https://github.com/immunogenomics/presto") (synopsis "Fast Functions for Differential Expression using Wilcox and AUC") (description "This package performs a fast Wilcoxon rank sum test and auROC analysis.") (license license:gpl3)))) (define-public r-sccustomize (let ((commit "397374590dae2ccc0c560897dcd1ce4382c18798") (revision "1")) (package (name "r-sccustomize") (version (git-version "2.0.1" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/samuel-marsh/scCustomize") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "11bafm0mlck27fqd8brz80pxb8dc5q0aqbp8zv0s9sx97njp7wsl")))) (properties `((upstream-name . "scCustomize"))) (build-system r-build-system) (propagated-inputs (list r-circlize r-colorway r-cowplot r-data-table r-dittoseq r-dplyr r-forcats r-ggbeeswarm r-ggplot2 r-ggprism r-ggpubr r-ggrastr r-ggrepel r-glue r-janitor r-magrittr r-matrix r-paletteer r-patchwork r-pbapply r-purrr r-remotes r-scales r-scattermore r-seurat r-seuratobject r-stringi r-stringr r-tibble r-tidyr r-tidyselect r-viridis)) (native-inputs (list r-knitr)) (home-page "https://github.com/samuel-marsh/scCustomize") (synopsis "Custom visualization and analyses of single-cell sequencing") (description "This is a collection of functions created and/or curated to aid in the visualization and analysis of single-cell data using R.") (license license:gpl3+)))) (define-public r-markdownhelpers (let ((commit "793372d28ebed607cc1d35f909a1caedb2b41ffe") (revision "1")) (package (name "r-markdownhelpers") (version (git-version "0.2.0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/vertesy/MarkdownHelpers") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "1d18s2ydhfjm3hjkxz42dirhwrrv792m6mvkmypallaa2qnwrmkg")))) (properties `((upstream-name . "MarkdownHelpers"))) (build-system r-build-system) (propagated-inputs (list r-devtools r-stringendo r-usethis)) (home-page "https://github.com/vertesy/MarkdownHelpers") (synopsis "Helper functions for MarkdownReports and ggExpress") (description "This package provides a set of R functions to parse markdown and other generic helpers.") (license license:gpl3)))) (define-public r-markdownreports (let ((commit "3ba1103e3ddc6df3a0c090eb884f5e65c461eb31") (revision "1")) (package (name "r-markdownreports") (version (git-version "4.5.9" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/vertesy/MarkdownReports") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "1xmasdb630b6nvxi5m1i8pyxiy49nxpzyxf9h8spdppx92rhdkc8")))) (properties `((upstream-name . "MarkdownReports"))) (build-system r-build-system) (propagated-inputs (list r-clipr r-codeandroll2 r-colorramps r-devtools r-gplots r-markdownhelpers r-rcolorbrewer r-readwriter r-sessioninfo r-sm r-stringendo r-venndiagram r-vioplot)) (home-page "https://github.com/vertesy/MarkdownReports") (synopsis "Tool for generating cientific figures and reports") (description "This is a set of R functions that allows you to generate precise figures. This tool will create clean markdown reports about what you just discovered.") (license license:gpl3)))) (define-public r-metacell (let ((commit "d6a6926d103ee0cb34a611c753572429c94a53d9") (revision "1")) (package (name "r-metacell") (version (git-version "0.3.41" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/tanaylab/metacell/") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0zrsckr3y35x37mj3ibm6scyqx925s84wzrz1i42fnm9n3msc265")))) (properties `((upstream-name . "metacell"))) (build-system r-build-system) (propagated-inputs (list r-cluster r-cowplot r-data-table r-dbscan r-domc r-dplyr r-entropy r-ggplot2 r-graph r-igraph r-kernsmooth r-magrittr r-matrix r-matrixstats r-pdist r-pheatmap r-plyr r-rcolorbrewer r-rcurl r-rgraphviz r-slam r-singlecellexperiment r-svglite r-tgconfig r-tgstat r-tgutil r-tidyr r-umap r-umap r-zoo)) (native-inputs (list r-knitr)) (home-page "https://github.com/tanaylab/metacell/") (synopsis "Meta cell analysis for single cell RNA-seq data") (description "This package facilitates the analysis of single-cell RNA-seq UMI matrices. It does this by computing partitions of a cell similarity graph into small homogeneous groups of cells, which are defined as metacells (MCs). The derived MCs are then used for building different representations of the data, allowing matrix or 2D graph visualization forming a basis for analysis of cell types, subtypes, transcriptional gradients,cell-cycle variation, gene modules and their regulatory models and more.") (license license:expat)))) (define-public r-metadeconfoundr ;; There are some relevant updates after the release of version 0.3.0. (let ((commit "90aec0226c5128bfcbbc08903452eff460d21424") (revision "1")) (package (name "r-metadeconfoundr") (version (git-version "0.3.0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/TillBirkner/metadeconfoundR") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0zkqar27p5qwq46xbxsw5x1pl50xbkgqiizw5bydlyhwb0ga2f3h")))) (properties `((upstream-name . "metadeconfoundR"))) (build-system r-build-system) (propagated-inputs (list r-bigmemory r-detectseparation r-doparallel r-dosnow r-foreach r-futile-logger r-ggplot2 r-lme4 r-lmtest r-reshape2 r-snow)) (native-inputs (list r-knitr)) (home-page "https://github.com/TillBirkner/metadeconfoundR") (synopsis "Check multiple covariates for potenial confounding effects") (description "This package detects naive associations between omics features and metadata in cross-sectional data-sets using non-parametric tests. In a second step, confounding effects between metadata associated to the same omics feature are detected and labeled using nested post-hoc model comparison tests. The generated output can be graphically summarized using the built-in plotting function.") (license license:gpl2)))) (define-public r-sleuth (package (name "r-sleuth") (version "0.30.1") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/pachterlab/sleuth") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "09xgc7r6iisjkk0c0wn0q56zy0aph386kphwixfzq4422y7vlqci")))) (properties `((upstream-name . "sleuth"))) (build-system r-build-system) (propagated-inputs (list r-aggregation r-data-table r-dplyr r-ggplot2 r-lazyeval r-matrixstats r-pheatmap r-reshape2 r-rhdf5 r-shiny r-tidyr)) (native-inputs (list r-knitr)) (home-page "https://github.com/pachterlab/sleuth") (synopsis "Tools for investigating RNA-Seq") (description "Sleuth is a program for differential analysis of RNA-Seq data. It makes use of quantification uncertainty estimates obtained via Kallisto for accurate differential analysis of isoforms or genes, allows testing in the context of experiments with complex designs, and supports interactive exploratory data analysis via sleuth live.") (license license:gpl3))) (define-public r-snapatac (package (name "r-snapatac") (version "2.0") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/r3fang/SnapATAC") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "037jzlbl436fi7lkpq7d83i2vd1crnrik3vac2x6xj75dbikb2av")))) (properties `((upstream-name . "SnapATAC"))) (build-system r-build-system) (propagated-inputs (list r-bigmemory r-doparallel r-dosnow r-edger r-foreach r-genomicranges r-igraph r-iranges r-irlba r-matrix r-plyr r-plot3d r-rann r-raster r-rcolorbrewer r-rhdf5 r-rtsne r-scales r-viridis)) (home-page "https://github.com/r3fang/SnapATAC") (synopsis "Single nucleus analysis package for ATAC-Seq") (description "This package provides a fast and accurate analysis toolkit for single cell ATAC-seq (Assay for transposase-accessible chromatin using sequencing). Single cell ATAC-seq can resolve the heterogeneity of a complex tissue and reveal cell-type specific regulatory landscapes. However, the exceeding data sparsity has posed unique challenges for the data analysis. This package @code{r-snapatac} is an end-to-end bioinformatics pipeline for analyzing large- scale single cell ATAC-seq data which includes quality control, normalization, clustering analysis, differential analysis, motif inference and exploration of single cell ATAC-seq sequencing data.") (license license:gpl3))) (define-public r-tsis (let ((commit "24460298fbe1d26e4da390f6e4f3d4d9d62334dc") (revision "1")) (package (name "r-tsis") (version (git-version "0.2.0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/wyguo/TSIS") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "17c8i25iwhldvs3c51m0wny40iffm8szzijalpwrxhzbv0xa94rb")))) (properties `((upstream-name . "TSIS"))) (build-system r-build-system) (native-inputs (list r-knitr)) (home-page "https://github.com/wyguo/TSIS") (synopsis "Time-series isoform switch of alternative splicing") (description "TSIS is used for detecting transcript isoform switches in time-series data. Transcript isoform switches occur when a pair of alternatively spliced isoforms reverse the order of their relative expression levels. TSIS characterizes the transcript switch by defining the isoform switch time-points for any pair of transcript isoforms within a gene. In addition, this tool describes the switch using five different features or metrics. Also it filters the results with user’s specifications and visualizes the results using different plots for the user to examine further details of the switches.") (license license:gpl3)))) (define-public r-umi4cpackage (let ((commit "88b07d896a137418ba6c31c2474b9dbe1d86fc20") (revision "1")) (package (name "r-umi4cpackage") (version (git-version "0.0.1" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/tanaylab/umi4cpackage") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0bjzamdw2lcfhlbzc0vdva87c3wwnij8jsvnrpx4wyyxvpcz13m5")))) (properties `((upstream-name . "umi4cPackage"))) (build-system r-build-system) (arguments `(#:phases (modify-phases %standard-phases (add-after 'unpack 'fix-references (lambda _ (substitute* "inst/conf/paths.conf" (("TG3C\\.bowtie2_bin=.*") (string-append "TG3C.bowtie2_bin=" (which "bowtie2") "\n"))) (substitute* "inst/perl/map3c/TG3C/import3C.pl" (("\"perl") (string-append "\"" (which "perl"))))))))) (inputs (list perl bowtie)) (propagated-inputs (list r-misha r-zoo)) (native-inputs (list r-knitr)) (home-page "https://github.com/tanaylab/umi4cpackage") (synopsis "Processing and analysis of UMI-4C contact profiles") (description "This is a package that lets you process UMI-4C data from scratch to produce nice plots.") (license license:expat)))) (define-public r-shinycell (let ((commit "aecbd56e66802f28e397f5ae1f19403aadd12163") (revision "1")) (package (name "r-shinycell") (version (git-version "2.0.0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/SGDDNB/ShinyCell") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "13jn2ikmvljnzayk485g1mmq5abcp9m1b8n1djdb1agmn83zaki5")))) (properties `((upstream-name . "ShinyCell"))) (build-system r-build-system) (propagated-inputs (list r-data-table r-ggplot2 r-glue r-gridextra r-hdf5r r-matrix r-r-utils r-rcolorbrewer r-readr r-reticulate)) (home-page "https://github.com/SGDDNB/ShinyCell") (synopsis "Shiny interactive web apps for single-cell data") (description "This package provides Shiny apps for interactive exploration of single-cell data.") (license license:gpl3)))) (define-public r-archr (let ((commit "c61b0645d1482f80dcc24e25fbd915128c1b2500") (revision "1")) (package (name "r-archr") (version (git-version "1.0.2" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/GreenleafLab/ArchR") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0sgdfd8iwgj8cssj2zr3gmshg8nv54q6dd8asjf99i39qkni7p9i")))) (properties `((upstream-name . "ArchR"))) (build-system r-build-system) (propagated-inputs (list r-biocgenerics r-biostrings r-chromvar r-complexheatmap r-data-table r-genomicranges r-ggplot2 r-ggrepel r-gridextra r-gtable r-gtools r-magrittr r-matrix r-matrixstats r-motifmatchr r-nabor r-plyr r-rcpp r-rhdf5 r-rsamtools r-s4vectors r-stringr r-summarizedexperiment r-uwot)) (home-page "https://github.com/GreenleafLab/ArchR") (synopsis "Analyze single-cell regulatory chromatin in R") (description "This package is designed to streamline scATAC analyses in R.") (license license:gpl2+)))) (define-public r-azimuth (let ((commit "243ee5db80fcbffa3452c944254a325a3da2ef9e") (revision "1")) (package (name "r-azimuth") (version (git-version "0.5.0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/satijalab/azimuth") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0vs4813kf2cv2j1z800ihwk62bw4dgmwgkd47rln58581chv39zm")))) (properties `((upstream-name . "Azimuth"))) (build-system r-build-system) (propagated-inputs (list r-bsgenome-hsapiens-ucsc-hg38 r-dt r-ensdb-hsapiens-v86 r-future r-ggplot2 r-glmgampoi r-googlesheets4 r-hdf5r r-htmltools r-httr r-jaspar2020 r-jsonlite r-matrix r-patchwork r-plotly r-presto r-rcpp r-rlang r-scales r-seurat r-seuratdata r-seuratdisk r-seuratobject r-shiny r-shinybs r-shinydashboard r-shinyjs r-signac r-stringr r-tfbstools r-withr)) (home-page "https://github.com/satijalab/azimuth") (synopsis "Shiny app showcasing a single-cell data query-reference mapping algorithm") (description "Azimuth utilizes an annotated reference dataset. It automates the processing, analysis, and interpretation. This applies specifically to new single-cell RNA-seq or ATAC-seq experiments. Azimuth leverages a reference-based mapping pipeline that inputs acounts matrix and performs normalization, visualization, cell annotation, and differential expression.") (license license:gpl3)))) (define-public r-icellnet ;; This is an arbitrary commit because there is no tag for 2.2.1. (let ((commit "e10ee4ae5feaf8130764dcb0736957d2a90b828c") (revision "1")) (package (name "r-icellnet") (version (git-version "2.2.1" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/soumelis-lab/ICELLNET") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0bszxw9zcsd1gxhg9q89jfzi95266wfjn74hp7z8yb99cr3j53k4")))) (build-system r-build-system) (arguments (list #:phases '(modify-phases %standard-phases (add-after 'unpack 'enter-dir (lambda _ (chdir "icellnet")))))) (propagated-inputs (list r-annotationdbi r-complexheatmap r-circlize r-data-table r-dplyr r-ggplot2 r-hgu133plus2-db r-jetset r-psych r-reshape2 r-rlist)) (home-page "https://github.com/soumelis-lab/ICELLNET") (synopsis "Transcriptomic-based framework to dissect cell communication") (description "This package provides a a transcriptomic-based framework to dissect cell communication in a global manner. It integrates an original expert-curated database of ligand-receptor interactions taking into account multiple subunits expression. Based on transcriptomic profiles (gene expression), this package computes communication scores between cells and provides several visualization modes that can be helpful to dig into cell-cell interaction mechanism and extend biological knowledge.") (license license:gpl3)))) (define-public r-scde (package (name "r-scde") (version "1.99.2") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/hms-dbmi/scde") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "10na2gyka24mszdxf92wz9h2c13hdf1ww30c68gfsw53lvvhhhxb")))) (build-system r-build-system) (propagated-inputs (list r-rcpp r-rcpparmadillo r-mgcv r-rook r-rjson r-cairo r-rcolorbrewer r-edger r-quantreg r-nnet r-rmtstat r-extremes r-pcamethods r-biocparallel r-flexmix)) (home-page "https://hms-dbmi.github.io/scde/") (synopsis "R package for analyzing single-cell RNA-seq data") (description "The SCDE package implements a set of statistical methods for analyzing single-cell RNA-seq data. SCDE fits individual error models for single-cell RNA-seq measurements. These models can then be used for assessment of differential expression between groups of cells, as well as other types of analysis. The SCDE package also contains the pagoda framework which applies pathway and gene set overdispersion analysis to identify aspects of transcriptional heterogeneity among single cells.") ;; See https://github.com/hms-dbmi/scde/issues/38 (license license:gpl2))) (define-public r-miamiplot (let ((commit "beede9c5d6431b4d822aa42e064e01baeb5dd4a0") (revision "1")) (package (name "r-miamiplot") (version (git-version "1.1.0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/juliedwhite/miamiplot") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0wxxk1lk9jbf0imf59qp302ffasvs84idinkvzirs3dw9w3589n9")))) (properties `((upstream-name . "miamiplot"))) (build-system r-build-system) (propagated-inputs (list r-checkmate r-dplyr r-ggplot2 r-ggrepel r-gridextra r-magrittr r-rlang)) (native-inputs (list r-knitr)) (home-page "https://github.com/juliedwhite/miamiplot") (synopsis "Create a ggplot2 miami plot") (description "This package generates a Miami plot with centered chromosome labels. The output is a ggplot2 object. Users can specify which data they want plotted on top vs. bottom, whether to display significance line(s), what colors to give chromosomes, and what points to label.") (license license:gpl2)))) (define-public r-millefy (package (name "r-millefy") (version "0.1.9-beta") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/yuifu/millefy") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "0z2y0x99f761pxvg6n37cmnyrnj699jhjk43pvk05sa86iykgizl")))) (properties `((upstream-name . "millefy"))) (build-system r-build-system) (propagated-inputs (list r-data-table r-destiny r-dplyr r-genomicranges r-iranges r-magrittr r-rsamtools r-rtracklayer r-tidyr)) (home-page "https://github.com/yuifu/millefy") (synopsis "Make millefy plot with single-cell RNA-seq data") (description "@code{Millefy} is a tool for visualizing read coverage of @dfn{scRNA-seq}(single-cell RNA sequencing) datasets in genomic contexts. By dynamically and automatically reorder single cells based on locus-specific pseudo time, @code{Millefy} highlights cell-to-cell heterogeneity in read coverage of scRNA-seq data.") (license license:expat))) (define-public r-misha (package (name "r-misha") (version "4.1.0") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/tanaylab/misha") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "0bgivx3lzjh3173jsfrhb5kvhjsn53br0n4hmyx7i3dwy2cnnp2p")) ;; Delete bundled executable. (snippet '(delete-file "exec/bigWigToWig")))) (build-system r-build-system) (arguments `(#:phases (modify-phases %standard-phases (add-after 'unpack 'do-not-use-bundled-bigWigToWig (lambda* (#:key inputs #:allow-other-keys) (substitute* "R/misha.R" (("get\$\".GLIBDIR\"\$, \"/exec/bigWigToWig") (string-append "\"" (assoc-ref inputs "kentutils") "/bin/bigWigToWig")))))))) (inputs (list kentutils)) (home-page "https://github.com/tanaylab/misha") (synopsis "Toolkit for analysis of genomic data") (description "This package is intended to help users to efficiently analyze genomic data resulting from various experiments.") (license license:gpl2))) (define-public r-scseqcomm (let ((commit "01076e703999f1a5aa76419d821b50aebe2b777a") (revision "0")) (package (name "r-scseqcomm") (version (git-version "0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://gitlab.com/sysbiobig/scseqcomm") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "1fw5si47d6agnz5fibmp2b1sv08pbpwv1j71w57xbav9044i032q")) ;; Delete bundled dependency. (modules '((guix build utils))) (snippet '(delete-file-recursively "other_deps")))) (build-system r-build-system) (inputs (list r-add2ggplot r-chorddiag r-doparallel r-dplyr r-foreach ;;r-grid ;; listed in DESCRIPTION r-gridextra r-ggplot2 r-gtable r-htmlwidgets r-igraph r-matrix ;;r-methods ;; listed in DESCRIPTION r-org-hs-eg-db r-psych r-rcolorbrewer r-rlang r-scico r-tidygraph r-topgo)) (native-inputs (list r-knitr)) (home-page "https://gitlab.com/sysbiobig/scseqcomm") (synopsis "Inter- and intra- cellular signaling from single cell RNA-seq") (description "This package is tools for analysing intercellular and intracellular signaling from single cell RNA-seq (scRNA-seq) data.") (license license:gpl3)))) (define-public r-shaman (let ((commit "d6944e8ac7bd1dbd5c6cec646eafc1d19d0ca96f") (release "2.0") (revision "2")) (package (name "r-shaman") (version (git-version release revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/tanaylab/shaman") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "03sx138dzpfiq23j49z0m0s4j79855mrg64hpj9c83408wzphxi6")) (snippet ;; This file will be generated. '(delete-file "inst/doc/shaman-package.R")))) (build-system r-build-system) (propagated-inputs (list r-data-table r-domc r-ggplot2 r-gviz r-misha r-plyr r-rann r-rcpp r-reshape2 ;; For vignettes r-rmarkdown r-knitr)) (home-page "https://github.com/tanaylab/shaman") (synopsis "Sampling HiC contact matrices for a-parametric normalization") (description "The Shaman package implements functions for resampling Hi-C matrices in order to generate expected contact distributions given constraints on marginal coverage and contact-distance probability distributions. The package also provides support for visualizing normalized matrices and statistical analysis of contact distributions around selected landmarks.") ;; Any version of the GPL (license license:gpl3+)))) (define-public r-centipede (package (name "r-centipede") (version "1.2") (source (origin (method url-fetch) (uri (string-append "http://download.r-forge.r-project.org/" "src/contrib/CENTIPEDE_" version ".tar.gz")) (sha256 (base32 "1hsx6qgwr0i67fhy9257zj7s0ppncph2hjgbia5nn6nfmj0ax6l9")))) (build-system r-build-system) (home-page "https://centipede.uchicago.edu/") (synopsis "Predict transcription factor binding sites") (description "CENTIPEDE applies a hierarchical Bayesian mixture model to infer regions of the genome that are bound by particular transcription factors. It starts by identifying a set of candidate binding sites, and then aims to classify the sites according to whether each site is bound or not bound by a transcription factor. CENTIPEDE is an unsupervised learning algorithm that discriminates between two different types of motif instances using as much relevant information as possible.") (license (list license:gpl2+ license:gpl3+)))) (define-public r-demultiplex (let ((commit "6e2a1422c8e6f418cfb271997eebc91f9195f299") (revision "1")) (package (name "r-demultiplex") (version (git-version "1.0.2" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/chris-mcginnis-ucsf/MULTI-seq") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "01kv88wp8vdaq07sjk0d3d1cb553mq1xqg0war81pgmg63bgi38w")))) (properties `((upstream-name . "deMULTIplex"))) (build-system r-build-system) (propagated-inputs (list r-kernsmooth r-reshape2 r-rtsne r-shortread r-stringdist)) (home-page "https://github.com/chris-mcginnis-ucsf/MULTI-seq") (synopsis "MULTI-seq pre-processing and classification tools") (description "deMULTIplex is an R package for analyzing single-cell RNA sequencing data generated with the MULTI-seq sample multiplexing method. The package includes software to @enumerate @item Convert raw MULTI-seq sample barcode library FASTQs into a sample barcode UMI count matrix, and @item Classify cell barcodes into sample barcode groups. @end enumerate ") (license license:cc0)))) (define-public r-demultiplex2 (let ((commit "e42bc8310c0ea035af100e6ccea59b46ad6385f5") (revision "1")) (package (name "r-demultiplex2") (version (git-version "1.0.0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/Gartner-Lab/deMULTIplex2") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "15f3kshsdvm97w24ql9b1wjlfbabimdsam0482hg7jivlvpl8j9w")))) (properties `((upstream-name . "deMULTIplex2"))) (build-system r-build-system) (propagated-inputs (list r-data-table r-devtools r-dplyr r-ggextra r-ggplot2 r-gridextra r-magrittr r-mass r-matrix r-rcolorbrewer r-shortread r-stringdist r-tidyr r-uwot r-viridis r-xvector)) (home-page "https://github.com/Gartner-Lab/deMULTIplex2") (synopsis "Robust sample demultiplexing for scRNA-seq") (description "This package implements a bioinformatics algorithm for demultiplexing multiplexed single cell datasets. It is built on a statistical model of tag read counts derived from the physical mechanism of tag cross-contamination.") (license license:cc0)))) (define-public r-demuxmix (let ((commit "09a7918ca6e0cd23e6bbaed2b97388bc499e248e") (revision "1")) (package (name "r-demuxmix") (version (git-version "1.1.1" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/huklein/demuxmix") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "03kfnns7m2447jsc3xplyv9qx8hvvdjmii7j837g3bb6smyxss96")))) (properties `((upstream-name . "demuxmix"))) (build-system r-build-system) (propagated-inputs (list r-ggplot2 r-gridextra r-mass r-matrix)) (native-inputs (list r-knitr)) (home-page "https://github.com/huklein/demuxmix") (synopsis "Demultiplexing oligo-barcoded scRNA-seq data using regression mixture models") (description "This package is used for demultiplexing single-cell sequencing experiments of pooled cells. These cells are labeled with barcode oligonucleotides. The package implements methods to fit regression mixture models for a probabilistic classification of cells, including multiplet detection. Demultiplexing error rates can be estimated, and methods for quality control are provided.") (license license:artistic2.0)))) (define-public gdc-client (package (name "gdc-client") (version "1.6.0") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/NCI-GDC/gdc-client.git") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "0cagawlzjwj3wam10lv64xgbfx4zcnzxi5sjpsdhq7rn4z24mzc2")))) (build-system python-build-system) (arguments `(#:phases (modify-phases %standard-phases (add-after 'unpack 'relax-requirements (lambda _ (substitute* "requirements.txt" (("==") ">="))))))) (inputs (list python-cryptography python-intervaltree python-jsonschema python-lxml python-ndg-httpsclient python-progressbar2 python-pyasn1 python-pyopenssl python-pyyaml python-requests python-termcolor)) (home-page "https://gdc.nci.nih.gov/access-data/gdc-data-transfer-tool") (synopsis "GDC data transfer tool") (description "The gdc-client provides several convenience functions over the GDC API which provides general download/upload via HTTPS.") (license license:asl2.0))) (define-public vsearch (package (name "vsearch") (version "2.9.1") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/torognes/vsearch") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "0vhrpjfdf75ba04b24xknp41790cvcgwl0vgpy7qbzj5xh2521ss")) (patches (search-patches "vsearch-unbundle-cityhash.patch")) (snippet '(begin ;; Remove bundled cityhash sources. The vsearch source is adjusted ;; for this in the patch. (delete-file "src/city.h") (delete-file "src/citycrc.h") (delete-file "src/city.cc") #t)))) (build-system gnu-build-system) (inputs (list zlib bzip2 cityhash)) (native-inputs (list autoconf automake)) (synopsis "Sequence search tools for metagenomics") (description "VSEARCH supports DNA sequence searching, clustering, chimera detection, dereplication, pairwise alignment, shuffling, subsampling, sorting and masking. The tool takes advantage of parallelism in the form of SIMD vectorization as well as multiple threads to perform accurate alignments at high speed. VSEARCH uses an optimal global aligner (full dynamic programming Needleman-Wunsch).") (home-page "https://github.com/torognes/vsearch") ;; vsearch uses non-portable SSE intrinsics so building fails on other ;; platforms. (supported-systems '("x86_64-linux")) ;; Dual licensed; also includes public domain source. (license (list license:gpl3 license:bsd-2)))) (define-public pairadise (package (name "pairadise") (version "1.0.0") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/Xinglab/PAIRADISE") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "0ycwcqabm4zdng0a7j593g35d5yzvvwm7dyi3b8s19zdi4rjzrwd")))) (build-system pyproject-build-system) (arguments (list #:phases '(modify-phases %standard-phases (add-after 'unpack 'chdir (lambda _ (chdir "pairadise"))) (add-before 'build '2to3 (lambda _ (invoke "2to3" "--write" "--nobackups" ".")))))) (inputs (list star)) (propagated-inputs (list python-pysam)) (home-page "https://github.com/Xinglab/PAIRADISE") (synopsis "Paired replicate analysis of allelic differential splicing events") (description "PAIRADISE is a method for detecting @dfn{allele-specific alternative splicing} (ASAS) from RNA-seq data. Unlike conventional approaches that detect ASAS events one sample at a time, PAIRADISE aggregates ASAS signals across multiple individuals in a population. By treating the two alleles of an individual as paired, and multiple individuals sharing a heterozygous SNP as replicates, PAIRADISE formulates ASAS detection as a statistical problem for identifying differential alternative splicing from RNA-seq data with paired replicates.") (license license:gpl3+))) (define-public r-pairadise (package (inherit pairadise) (name "r-pairadise") (build-system r-build-system) (arguments (list #:phases '(modify-phases %standard-phases (add-after 'unpack 'chdir (lambda _ (chdir "pairadise/src/pairadise_model")))))) (inputs '()) (propagated-inputs (list r-doparallel r-foreach r-iterators r-nloptr)) (license license:expat))) (define-public pardre (package (name "pardre") (version "2.2.5") (source (origin (method url-fetch) (uri (string-append "mirror://sourceforge/pardre/ParDRe-rel" version ".tar.gz")) (sha256 (base32 "105s4f8zs8hh0sc32r9p725n7idza9cj5jvp5z1m5pljjhgk3if5")))) (build-system gnu-build-system) (arguments `(#:tests? #f ; tests require "prove" #:phases (modify-phases %standard-phases (delete 'configure) (replace 'install (lambda* (#:key outputs #:allow-other-keys) (let ((bin (string-append (assoc-ref outputs "out") "/bin"))) (install-file "ParDRe" bin))))))) (inputs (list openmpi-c++ zlib)) (synopsis "Parallel tool to remove duplicate DNA reads") (description "ParDRe is a parallel tool to remove duplicate genetic sequence reads. Duplicate reads can be seen as identical or nearly identical sequences with some mismatches. This tool lets users avoid the analysis of unnecessary reads, reducing the time of subsequent procedures with the dataset (e.g. assemblies, mappings, etc.). The tool is implemented with MPI in order to exploit the parallel capabilities of multicore clusters. It is faster than multithreaded counterparts (end of 2015) for the same number of cores and, thanks to the message-passing technology, it can be executed on clusters.") (home-page "https://sourceforge.net/projects/pardre/") (license license:gpl3+))) (define-public ngshmmalign (package (name "ngshmmalign") (version "0.1.1") (source (origin (method url-fetch) (uri (string-append "https://github.com/cbg-ethz/ngshmmalign/" "releases/download/" version "/ngshmmalign-" version ".tar.bz2")) (sha256 (base32 "0jryvlssi2r2ii1dxnx39yk6bh4yqgq010fnxrgfgbaj3ykijlzv")))) (build-system cmake-build-system) (arguments '(#:tests? #false)) ; there are none (inputs (list boost)) (home-page "https://github.com/cbg-ethz/ngshmmalign/") (synopsis "Profile HMM aligner for NGS reads") (description "ngshmmalign is a profile HMM aligner for NGS reads designed particularly for small genomes (such as those of RNA viruses like HIV-1 and HCV) that experience substantial biological insertions and deletions.") (license license:gpl2+))) (define-public prinseq (package (name "prinseq") (version "0.20.4") (source (origin (method url-fetch) (uri (string-append "mirror://sourceforge/prinseq/standalone/" "prinseq-lite-" version ".tar.gz")) (sha256 (base32 "0vxmzvmm67whxrqdaaamwgjk7cf0fzfs5s673jgg00kz7g70splv")))) (build-system gnu-build-system) (arguments `(#:tests? #false ; no check target #:phases (modify-phases %standard-phases (delete 'configure) (delete 'build) (replace 'install (lambda* (#:key inputs outputs #:allow-other-keys) (let* ((out (assoc-ref outputs "out")) (bin (string-append out "/bin")) (scripts (find-files "." "prinseq.*.pl")) (guile (search-input-file inputs "bin/guile"))) (substitute* scripts (("\"perl -pe") (string-append "\"" (which "perl") " -pe"))) (for-each (lambda (file) (chmod file #o555) (install-file file bin) (wrap-script (string-append bin "/" (basename file)) #:guile guile `("PERL5LIB" ":" prefix (,(getenv "PERL5LIB"))))) scripts))))))) (inputs (list guile-3.0 ; for wrapper scripts perl perl-cairo perl-data-dumper perl-digest-md5 perl-getopt-long perl-json perl-statistics-pca)) (home-page "https://prinseq.sourceforge.net/") (synopsis "Preprocess sequence data in FASTA or FASTQ formats") (description "PRINSEQ is a bioinformatics tool to help you preprocess your genomic or metagenomic sequence data in FASTA or FASTQ formats. The tool is written in Perl and can be helpful if you want to filter, reformat, or trim your sequence data. It also generates basic statistics for your sequences.") (license license:gpl3+))) (define-public shorah (package (name "shorah") (version "1.99.2") (source (origin (method url-fetch) (uri (string-append "https://github.com/cbg-ethz/shorah" "/releases/download/v" version "/shorah-" version ".tar.xz")) (sha256 (base32 "158dir9qcqspknlnyfr9zwk41x48nrh5wcg10k2grh9cidp9daiq")))) (build-system gnu-build-system) (arguments `(#:phases (modify-phases %standard-phases (add-after 'unpack 'fix-test-wrapper (lambda* (#:key outputs #:allow-other-keys) (let ((bin (string-append (assoc-ref outputs "out") "/bin"))) (substitute* "examples/run_end2end_test" (("\\$\\{interpreter\\} ../\\$\\{testscript\\}") (string-append bin "/${testscript}")))))) (delete 'check) (add-after 'install 'wrap-programs (lambda* (#:key outputs #:allow-other-keys) (let* ((out (assoc-ref outputs "out")) (site (string-append out "/lib/python" ,(version-major+minor (package-version python)) "/site-packages")) (pythonpath (getenv "GUIX_PYTHONPATH")) (script (string-append out "/bin/shorah"))) (chmod script #o555) (wrap-program script `("GUIX_PYTHONPATH" ":" prefix (,site ,pythonpath)))))) (add-after 'wrap-programs 'check (lambda* (#:key tests? #:allow-other-keys) (when tests? (invoke "make" "check"))))))) (inputs (list bash-minimal boost htslib python python-biopython python-numpy zlib)) (native-inputs (list pkg-config)) (home-page "") (synopsis "Short reads assembly into haplotypes") (description "ShoRAH is a project for the analysis of next generation sequencing data. It is designed to analyse genetically heterogeneous samples. Its tools provide error correction, haplotype reconstruction and estimation of the frequency of the different genetic variants present in a mixed sample.") (license license:gpl3+))) (define-public ruby-bio-kseq (package (name "ruby-bio-kseq") (version "0.0.2") (source (origin (method url-fetch) (uri (rubygems-uri "bio-kseq" version)) (sha256 (base32 "1xyaha46khb5jc6wzkbf7040jagac49jbimn0vcrzid0j8jdikrz")))) (build-system ruby-build-system) (arguments `(#:test-target "spec")) (native-inputs (list bundler ruby-rspec ruby-rake-compiler)) (inputs (list zlib)) (synopsis "Ruby bindings for the kseq.h FASTA/Q parser") (description "@code{Bio::Kseq} provides ruby bindings to the @code{kseq.h} FASTA and FASTQ parsing code. It provides a fast iterator over sequences and their quality scores.") (home-page "https://github.com/gusevfe/bio-kseq") (license license:expat))) (define-public bio-locus (package (name "bio-locus") (version "0.0.7") (source (origin (method url-fetch) (uri (rubygems-uri "bio-locus" version)) (sha256 (base32 "02vmrxyimkj9sahsp4zhfhnmbvz6dbbqz1y01vglf8cbwvkajfl0")))) (build-system ruby-build-system) (native-inputs (list ruby-rspec)) (synopsis "Tool for fast querying of genome locations") (description "Bio-locus is a tabix-like tool for fast querying of genome locations. Many file formats in bioinformatics contain records that start with a chromosome name and a position for a SNP, or a start-end position for indels. Bio-locus allows users to store this chr+pos or chr+pos+alt information in a database.") (home-page "https://github.com/pjotrp/bio-locus") (license license:expat))) (define-public bio-blastxmlparser (package (name "bio-blastxmlparser") (version "2.0.4") (source (origin (method url-fetch) (uri (rubygems-uri "bio-blastxmlparser" version)) (sha256 (base32 "1wf4qygcmdjgcqm6flmvsagfr1gs9lf63mj32qv3z1f481zc5692")))) (build-system ruby-build-system) (propagated-inputs (list ruby-bio-logger ruby-nokogiri)) (inputs (list ruby-rspec)) (synopsis "Fast big data BLAST XML parser and library") (description "Very fast parallel big-data BLAST XML file parser which can be used as command line utility. Use blastxmlparser to: Parse BLAST XML; filter output; generate FASTA, JSON, YAML, RDF, JSON-LD, HTML, CSV, tabular output etc.") (home-page "https://github.com/pjotrp/blastxmlparser") (license license:expat))) (define-public bioruby (package (name "bioruby") (version "2.0.4") (source (origin (method url-fetch) (uri (rubygems-uri "bio" version)) (sha256 (base32 "08aknxk2ingwscwfqpw5vnax6jpk1sxfaialravladb63hcl8dx9")))) (build-system ruby-build-system) (propagated-inputs (list ruby-libxml)) (native-inputs (list which)) ; required for test phase (arguments (list #:phases #~(modify-phases %standard-phases (add-before 'build 'patch-test-command (lambda _ (substitute* '("test/functional/bio/test_command.rb") (("/bin/sh") (which "sh"))) (substitute* '("test/functional/bio/test_command.rb") (("/bin/ls") (which "ls"))) (substitute* '("test/functional/bio/test_command.rb") (("which") (which "which"))) (substitute* '("test/functional/bio/test_command.rb" "test/data/command/echoarg2.sh") (("/bin/echo") (which "echo")))))))) (synopsis "Ruby library, shell and utilities for bioinformatics") (description "BioRuby comes with a comprehensive set of Ruby development tools and libraries for bioinformatics and molecular biology. BioRuby has components for sequence analysis, pathway analysis, protein modelling and phylogenetic analysis; it supports many widely used data formats and provides easy access to databases, external programs and public web services, including BLAST, KEGG, GenBank, MEDLINE and GO.") (home-page "http://bioruby.org/") ;; Code is released under Ruby license, except for setup ;; (LGPLv2.1+) and scripts in samples (which have GPL2 and GPL2+) (license (list license:ruby license:lgpl2.1+ license:gpl2+ )))) (define-public centrifuge (package (name "centrifuge") (version "1.0.4") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/DaehwanKimLab/centrifuge.git") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "167610gbz1rrh6ir3j7jcmhzg3x5msn7x7a3dpv7wmwdndnnqvg0")))) (build-system gnu-build-system) (arguments (list #:tests? #false ; no check target #:make-flags #~(list (string-append "prefix=" #$output)) #:phases '(modify-phases %standard-phases (delete 'configure)))) (inputs (list python-wrapper)) (native-inputs (list pandoc perl ;for documentation which)) (home-page "https://github.com/DaehwanKimLab/centrifuge/") (synopsis "Classifier for metagenomic sequences") (description "Centrifuge is a microbial classification engine that enables rapid, accurate and sensitive labeling of reads and quantification of species on desktop computers. The system uses an indexing scheme based on the @dfn{Burrows-Wheeler transform} (BWT) and the @dfn{Ferragina-Manzini} (FM) index, optimized specifically for the metagenomic classification problem. Centrifuge requires a relatively small index (4.7 GB for all complete bacterial and viral genomes plus the human genome) and classifies sequences at very high speed, allowing it to process the millions of reads from a typical high-throughput DNA sequencing run within a few minutes.") (license license:gpl3+))) (define-public bio-vcf (package (name "bio-vcf") (version "0.9.5") (source (origin (method url-fetch) (uri (rubygems-uri "bio-vcf" version)) (sha256 (base32 "1glw5pn9s8z13spxk6yyfqaz80n9lga67f33w35nkpq9dwi2vg6g")))) (build-system ruby-build-system) (native-inputs (list ruby-cucumber)) (synopsis "Smart VCF parser DSL") (description "Bio-vcf provides a @acronym{DSL, domain specific language} for processing the VCF format. Record named fields can be queried with regular expressions. Bio-vcf is a new generation VCF parser, filter and converter. Bio-vcf is not only very fast for genome-wide (WGS) data, it also comes with a filtering, evaluation and rewrite language and can output any type of textual data, including VCF header and contents in RDF and JSON.") (home-page "https://github.com/vcflib/bio-vcf") (license license:expat))) (define-public r-phantompeakqualtools (let ((commit "8d2b2d18c686d894ef5908b37da7adf72a07ef42") (revision "1")) (package (name "r-phantompeakqualtools") (version (git-version "1.2.2" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/kundajelab/phantompeakqualtools") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "00anrvcwsp02d98qhj1xpj85644h2pp4kfzq6dgbmwmdr6jvy7p4")))) (build-system gnu-build-system) (arguments `(#:tests? #f ; There are no tests. #:phases (modify-phases %standard-phases (delete 'configure) (delete 'build) (replace 'install (lambda* (#:key inputs outputs #:allow-other-keys) (let ((script (string-append (assoc-ref outputs "out") "/share/scripts"))) (install-file "run_spp.R" script))))))) (inputs `(("r" ,r-minimal))) (propagated-inputs (list r-catools r-snow r-snowfall r-bitops r-rsamtools r-spp gawk samtools boost gzip)) (home-page "https://github.com/kundajelab/phantompeakqualtools") (synopsis "Informative enrichment for ChIP-seq data") (description "This package computes informative enrichment and quality measures for ChIP-seq/DNase-seq/FAIRE-seq/MNase-seq data. It can also be used to obtain robust estimates of the predominant fragment length or characteristic tag shift values in these assays.") (license license:bsd-3)))) (define-public r-r4rna (package (name "r-r4rna") (version "0.1.4") (source (origin (method url-fetch) (uri (string-append "http://www.e-rna.org/r-chie/files/R4RNA_" version ".tar.gz")) (sha256 (base32 "1p0i78wh76jfgmn9jphbwwaz6yy6pipzfg08xs54cxavxg2j81p5")))) (build-system r-build-system) (propagated-inputs (list r-optparse r-rcolorbrewer)) (home-page "https://www.e-rna.org/r-chie/index.cgi") (synopsis "Analysis framework for RNA secondary structure") (description "The R4RNA package aims to be a general framework for the analysis of RNA secondary structure and comparative analysis in R.") (license license:gpl3+))) (define-public rcas-web (let ((commit "71c93e3835653beb4eaa6e89b860bee3779729b8") (revision "2")) (package (name "rcas-web") (version (git-version "0.1.0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/BIMSBbioinfo/rcas-web") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0232g0f7g0w5cgaib462zbfssvfq8i0iqv5b5wfmbrbn0sw99l9a")))) (build-system gnu-build-system) (arguments (list #:phases #~(modify-phases %standard-phases (add-after 'install 'wrap-executable (lambda* (#:key inputs outputs #:allow-other-keys) (let* ((json #$(this-package-input "guile-json")) (redis #$(this-package-input "guile-redis")) (path (string-append json "/share/guile/site/3.0:" redis "/share/guile/site/3.0"))) (wrap-program (string-append #$output "/bin/rcas-web") `("GUILE_LOAD_PATH" ":" = (,path)) `("GUILE_LOAD_COMPILED_PATH" ":" = (,path)) `("R_LIBS_SITE" ":" = (,(getenv "R_LIBS_SITE")))))))))) (inputs (list bash-minimal r-minimal r-rcas guile-3.0 guile-json-4 guile-redis)) (native-inputs (list autoconf automake pkg-config)) (home-page "https://github.com/BIMSBbioinfo/rcas-web") (synopsis "Web interface for RNA-centric annotation system (RCAS)") (description "This package provides a simple web interface for the @dfn{RNA-centric annotation system} (RCAS).") (license license:agpl3+)))) (define-public r-chipkernels (let ((commit "c9cfcacb626b1221094fb3490ea7bac0fd625372") (revision "1")) (package (name "r-chipkernels") (version (git-version "1.1" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/ManuSetty/ChIPKernels") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "14bj5qhjm1hsm9ay561nfbqi9wxsa7y487df2idsaaf6z10nw4v0")))) (build-system r-build-system) (propagated-inputs (list r-iranges r-xvector r-biostrings r-bsgenome r-gtools r-genomicranges r-sfsmisc r-kernlab r-s4vectors r-biocgenerics)) (home-page "https://github.com/ManuSetty/ChIPKernels") (synopsis "Build string kernels for DNA Sequence analysis") (description "ChIPKernels is an R package for building different string kernels used for DNA Sequence analysis. A dictionary of the desired kernel must be built and this dictionary can be used for determining kernels for DNA Sequences.") (license license:gpl2+)))) (define-public r-seqgl (package (name "r-seqgl") (version "1.1.4") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/ManuSetty/SeqGL") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "1r6ywvhxl3ffv48lgj7sbd582mcc6dha3ksgc2qjlvjrnkbj3799")))) (build-system r-build-system) (propagated-inputs (list r-biostrings r-chipkernels r-genomicranges r-spams r-wgcna r-fastcluster)) (home-page "https://github.com/ManuSetty/SeqGL") (synopsis "Group lasso for Dnase/ChIP-seq data") (description "SeqGL is a group lasso based algorithm to extract transcription factor sequence signals from ChIP, DNase and ATAC-seq profiles. This package presents a method which uses group lasso to discriminate between bound and non bound genomic regions to accurately identify transcription factors bound at the specific regions.") (license license:gpl2+))) (define-public r-seraster ;; There are no tags or releases. (let ((commit "4fdc1ffe5d3feb65de9880329d221cf276b393a1") (revision "1")) (package (name "r-seraster") (version (git-version "0.99.0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/JEFworks-Lab/SEraster") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0y33lk8q0h9nfzmf7slxxvw3l0djassp4l63nsjpm3p6z4pah5s4")))) (properties `((upstream-name . "SEraster"))) (build-system r-build-system) (propagated-inputs (list r-biocparallel r-ggplot2 r-matrix r-rearrr r-sf r-spatialexperiment r-summarizedexperiment)) (home-page "https://github.com/JEFworks-Lab/SEraster") (synopsis "Rasterization framework for scalable spatial omics data analysis") (description "This package is a rasterization preprocessing framework that aggregates cellular information into spatial pixels to reduce resource requirements for spatial omics data analysis. SEraster reduces the number of points in spatial omics datasets for downstream analysis through a process of rasterization where single cells gene expression or cell-type labels are aggregated into equally sized pixels based on a user-defined resolution. SEraster can be incorporated with other packages to conduct downstream analyses for spatial omics datasets, such as detecting spatially variable genes.") (license license:gpl3)))) (define-public emboss (package (name "emboss") (version "6.5.7") (source (origin (method url-fetch) (uri (string-append "ftp://emboss.open-bio.org/pub/EMBOSS/old/" (version-major+minor version) ".0/" "EMBOSS-" version ".tar.gz")) (sha256 (base32 "0vsmz96gc411yj2iyzdrsmg4l2n1nhgmp7vrgzlxx3xixv9xbf0q")))) (build-system gnu-build-system) (arguments `(#:configure-flags ,#~(list (string-append "--with-hpdf=" #$(this-package-input "libharu"))) #:phases (modify-phases %standard-phases (add-after 'unpack 'fix-checks (lambda _ ;; The PNGDRIVER tests check for the presence of libgd, libpng ;; and zlib, but assume that they are all found at the same ;; prefix. (substitute* "configure.in" (("CHECK_PNGDRIVER") "LIBS=\"$LIBS -lgd -lpng -lz -lm\" AC_DEFINE([PLD_png], [1], [Define to 1 if PNG support is available]) AM_CONDITIONAL(AMPNG, true)")) #t)) (add-after 'fix-checks 'disable-update-check (lambda _ ;; At build time there is no connection to the Internet, so ;; looking for updates will not work. (substitute* "Makefile.am" (("\\$\$bindir\$/embossupdate") "")) #t)) (add-after 'disable-update-check 'autogen (lambda _ (invoke "autoreconf" "-vif") #t))))) (inputs (list perl libpng gd libx11 libharu zlib)) (native-inputs (list autoconf automake libtool pkg-config)) (home-page "https://emboss.sourceforge.net") (synopsis "Molecular biology analysis suite") (description "EMBOSS is the \"European Molecular Biology Open Software Suite\". EMBOSS is an analysis package specially developed for the needs of the molecular biology (e.g. EMBnet) user community. The software automatically copes with data in a variety of formats and even allows transparent retrieval of sequence data from the web. It also provides a number of libraries for the development of software in the field of molecular biology. EMBOSS also integrates a range of currently available packages and tools for sequence analysis into a seamless whole.") (license license:gpl2+))) (define-public bits (let ((revision "1") (commit "3cc4567896d9d6442923da944beb704750a08d2d")) (package (name "bits") ;; The version is 2.13.0 even though no release archives have been ;; published as yet. (version (git-version "2.13.0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/arq5x/bits") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "17n2kffk4kmhivd8c98g2vr6y1s23vbg4sxlxs689wni66797hbs")))) (build-system gnu-build-system) (arguments `(#:tests? #f ;no tests included #:phases (modify-phases %standard-phases (delete 'configure) (add-after 'unpack 'remove-cuda (lambda _ (substitute* "Makefile" ((".*_cuda") "") (("(bits_test_intersections) \\\\" _ match) match)) #t)) (replace 'install (lambda* (#:key outputs #:allow-other-keys) (copy-recursively "bin" (string-append (assoc-ref outputs "out") "/bin")) #t))))) (inputs (list gsl zlib)) (home-page "https://github.com/arq5x/bits") (synopsis "Implementation of binary interval search algorithm") (description "This package provides an implementation of the BITS (Binary Interval Search) algorithm, an approach to interval set intersection. It is especially suited for the comparison of diverse genomic datasets and the exploration of large datasets of genome intervals (e.g. genes, sequence alignments).") (license license:gpl2)))) (define-public piranha ;; There is no release tarball for the latest version. The latest commit is ;; older than one year at the time of this writing. (let ((revision "1") (commit "0466d364b71117d01e4471b74c514436cc281233")) (package (name "piranha") (version (git-version "1.2.1" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/smithlabcode/piranha") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "117dc0zf20c61jam69sk4abl57ah6yi6i7qra7d7y5zrbgk12q5n")))) (build-system gnu-build-system) (arguments `(#:test-target "test" #:phases (modify-phases %standard-phases (add-after 'unpack 'copy-smithlab-cpp (lambda* (#:key inputs #:allow-other-keys) (for-each (lambda (file) (install-file file "./src/smithlab_cpp/")) (find-files (assoc-ref inputs "smithlab-cpp"))))) (add-after 'install 'install-to-store (lambda* (#:key outputs #:allow-other-keys) (let* ((out (assoc-ref outputs "out")) (bin (string-append out "/bin"))) (for-each (lambda (file) (install-file file bin)) (find-files "bin" ".*")))))) #:configure-flags ,#~(list (string-append "--with-bam_tools_headers=" #$(this-package-input "bamtools") "/include/bamtools") (string-append "--with-bam_tools_library=" #$(this-package-input "bamtools") "/lib/bamtools")))) (inputs `(("bamtools" ,bamtools) ("samtools" ,samtools-0.1) ("gsl" ,gsl) ("smithlab-cpp" ,(let ((commit "3723e2db438c51501d0423429ff396c3035ba46a")) (origin (method git-fetch) (uri (git-reference (url "https://github.com/smithlabcode/smithlab_cpp") (commit commit))) (file-name (string-append "smithlab_cpp-" commit "-checkout")) (sha256 (base32 "0l4gvbwslw5ngziskja41c00x1r06l3yidv7y0xw9djibhykzy0g"))))))) (native-inputs `(("python" ,python-2))) (home-page "https://github.com/smithlabcode/piranha") (synopsis "Peak-caller for CLIP-seq and RIP-seq data") (description "Piranha is a peak-caller for genomic data produced by CLIP-seq and RIP-seq experiments. It takes input in BED or BAM format and identifies regions of statistically significant read enrichment. Additional covariates may optionally be provided to further inform the peak-calling process.") (license license:gpl3+)))) (define-public filevercmp (let ((commit "1a9b779b93d0b244040274794d402106907b71b7") (revision "1")) (package (name "filevercmp") (version (git-version "0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/ekg/filevercmp") (commit commit))) (file-name (git-file-name name commit)) (sha256 (base32 "1j9vxsy0y050v59h0q1d6501fcw1kjvj0d18l1xk2zyg0jzj247c")))) (build-system gnu-build-system) (arguments `(#:tests? #f ; There are no tests to run. #:phases (modify-phases %standard-phases (delete 'configure) ; There is no configure phase. (replace 'install (lambda* (#:key outputs #:allow-other-keys) (let ((out (assoc-ref outputs "out"))) (install-file "filevercmp" (string-append out "/bin")) (install-file "filevercmp.h" (string-append out "/include")) #t)))))) (home-page "https://github.com/ekg/filevercmp") (synopsis "This program compares version strings") (description "This program compares version strings. It intends to be a replacement for strverscmp.") (license license:gpl3+)))) (define-public multiqc (package (name "multiqc") (version "1.14") (source (origin (method url-fetch) (uri (pypi-uri "multiqc" version)) (sha256 (base32 "0qlk2h0765hxp1w9hqf925rh8hq642lzgs6ppg91wln9y02s9fyw")))) (build-system pyproject-build-system) (arguments `(#:phases (modify-phases %standard-phases (replace 'check (lambda* (#:key inputs tests? #:allow-other-keys) (when tests? (setenv "HOME" "/tmp") (let ((here (getcwd))) (copy-recursively (assoc-ref inputs "tests") "/tmp/tests") (with-directory-excursion "/tmp/tests" (invoke "multiqc" "data" "--ignore" "data/modules"))))))))) (inputs (list python-click python-coloredlogs python-future python-jinja2 python-lzstring python-markdown python-matplotlib python-networkx python-numpy python-pyyaml python-requests python-rich python-rich-click python-simplejson python-spectra)) (native-inputs `(("python-pytest" ,python-pytest) ("tests" ,(let ((commit "c3e7400affe3f3ca996973805797af61b93070ba")) (origin (method git-fetch) (uri (git-reference (url "https://github.com/ewels/MultiQC_TestData") (commit commit))) (file-name (git-file-name "multiqc-test-data" commit)) (sha256 (base32 "0wwqbkbfnqj5ax6l0da4csbmv1sw7ya7mwvdwryckaiqmkxy80va"))))))) (home-page "https://multiqc.info") (synopsis "Aggregate bioinformatics analysis reports") (description "MultiQC is a tool to aggregate bioinformatics results across many samples into a single report. It contains modules for a large number of common bioinformatics tools.") (license license:gpl3+))) (define-public variant-tools (package (name "variant-tools") (version "3.1.2") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/vatlab/varianttools") ;; There is no tag corresponding to version 3.1.2 (commit "813ae4a90d25b69abc8a40f4f70441fe09015249"))) (file-name (git-file-name name version)) (sha256 (base32 "12ibdmksj7icyqhks4xyvd61bygk4pjmxn618kp6vgk1af01y34g")))) (build-system python-build-system) (inputs (list boost c-blosc gsl hdf5 hdf5-blosc python-cython zlib)) (propagated-inputs (list python-numpy python-pycurl python-pyzmq python-scipy python-tables)) (home-page "https://vatlab.github.io/vat-docs/") (synopsis "Analyze genetic variants from Next-Gen sequencing studies") (description "Variant tools is a tool for the manipulation, annotation, selection, simulation, and analysis of variants in the context of next-gen sequencing analysis. Unlike some other tools used for next-gen sequencing analysis, variant tools is project based and provides a whole set of tools to manipulate and analyze genetic variants.") (license license:gpl3+))) (define-public r-chromvarmotifs (let ((commit "38bed559c1f4770b6c91c80bf3f8ea965da26076") (revision "1")) (package (name "r-chromvarmotifs") (version (git-version "0.2.0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/GreenleafLab/chromVARmotifs") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0i9v1m1hrg1lkd2pnkj5nnrpks6vhhhpbdhsfl2lmjak4npxxr5q")))) (properties `((upstream-name . "chromVARmotifs"))) (build-system r-build-system) (propagated-inputs `(("r-tfbstools" ,r-tfbstools))) (home-page "https://github.com/GreenleafLab/chromVARmotifs") (synopsis "Stores motif collections for use with motifmatchr or chromVAR") (description "This package stores motif collections as lists of @dfn{position frequency matrix} (PWMatrixList) objects provided by the @code{TFBSTools} package for use in R with packages like @code{motifmatchr} or @code{chromVAR}.") (license license:expat)))) (define-public r-raremetals2 (package (name "r-raremetals2") (version "0.1") (source (origin (method url-fetch) (uri (string-append "http://genome.sph.umich.edu/w/images/" "b/b7/RareMETALS2_" version ".tar.gz")) (sha256 (base32 "0z5ljcgvnm06ja9lm85a3cniq7slxcy37aqqkxrdidr79an5fs4s")))) (properties `((upstream-name . "RareMETALS2"))) (build-system r-build-system) (propagated-inputs (list r-seqminer r-mvtnorm r-mass r-compquadform r-getopt)) (home-page "http://genome.sph.umich.edu/wiki/RareMETALS2") (synopsis "Analyze gene-level association tests for binary trait") (description "The R package rareMETALS2 is an extension of the R package rareMETALS. It was designed to meta-analyze gene-level association tests for binary trait. While rareMETALS offers a near-complete solution for meta-analysis of gene-level tests for quantitative trait, it does not offer the optimal solution for binary trait. The package rareMETALS2 offers improved features for analyzing gene-level association tests in meta-analyses for binary trait.") (license license:gpl3))) (define-public r-rnacrosslinkoo (let ((commit "a317e0fa6ddf34c309529d57390769e2b2b5bfb7") (revision "1")) (package (name "r-rnacrosslinkoo") (version (git-version "0.1.3" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/cran/rnaCrosslinkOO") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0csv9924z0ish960k034qzv3gxh1yabnxni8hsrn5j6xl1r3cdpl")))) (properties `((upstream-name . "rnaCrosslinkOO"))) (build-system r-build-system) (propagated-inputs (list r-classdiscovery r-doparallel r-foreach r-genomicranges r-ggplot2 r-ggrepel r-heatmap3 r-igraph r-iranges r-mass r-mixtools r-patchwork r-r4rna r-rcolorbrewer r-reshape2 r-rrna r-s4vectors r-seqinr r-tidyverse r-topdom)) (native-inputs (list r-knitr)) (home-page "https://github.com/cran/rnaCrosslinkOO") (synopsis "Analysis of RNA crosslinking data") (description "The package is ideal for analyzing RNA structure and chemical probing data.") (license license:gpl3)))) (define-public r-rnaseqdtu (let ((commit "5bee1e769d2e1dc6a3f1cecb78078050eeb5b9ac") (revision "1")) (package (name "r-rnaseqdtu") (version (git-version "2.0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/mikelove/rnaseqDTU/") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0jfi1ydsk8m5nadwnih48v87nnxdc7s3f0pny4axmnj40dd42as0")))) (properties `((upstream-name . "rnaseqDTU"))) (build-system r-build-system) (propagated-inputs (list r-deseq2 r-devtools r-dexseq r-drimseq r-edger r-rafalib r-stager)) (native-inputs (list r-knitr)) (home-page "https://github.com/mikelove/rnaseqDTU/") (synopsis "RNA-seq workflow for differential transcript usage") (description "This package provides an RNA-seq workflow for differential transcript usage (DTU) following Salmon quantification. This workflow performs a DTU analysis on simulated data. It also shows how to use stageR to perform two-stage testing of DTU, a statistical framework to screen at the gene level and then confirm which transcripts within the significant genes show evidence of DTU.") (license license:artistic2.0)))) (define-public r-dropbead (let ((commit "d746c6f3b32110428ea56d6a0001ce52a251c247") (revision "2")) (package (name "r-dropbead") (version (string-append "0-" revision "." (string-take commit 7))) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/rajewsky-lab/dropbead") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0sbzma49aiiyw8b0jpr7fnhzys9nsqmp4hy4hdz1gzyg1lhnca26")))) (build-system r-build-system) (propagated-inputs (list r-ggplot2 r-rcolorbrewer r-gridextra r-gplots r-plyr)) (home-page "https://github.com/rajewsky-lab/dropbead") (synopsis "Basic exploration and analysis of Drop-seq data") (description "This package offers a quick and straight-forward way to explore and perform basic analysis of single cell sequencing data coming from droplet sequencing. It has been particularly tailored for Drop-seq.") (license license:gpl3)))) (define-public r-cellchat (let ((commit "21edd226ca408e4c413408f98562d71ee0b54e5d") (revision "1")) (package (name "r-cellchat") (version (git-version "1.0.0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/sqjin/CellChat") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0cvzl9mi8jjznpql2gv67swnk1dndn3a2h22z5l84h7lwpwjmh53")) (snippet '(for-each delete-file '("src/CellChat.so" "src/CellChat_Rcpp.o" "src/RcppExports.o"))))) (properties `((upstream-name . "CellChat"))) (build-system r-build-system) (propagated-inputs (list r-biocgenerics r-circlize r-colorspace r-complexheatmap r-cowplot r-dplyr r-expm r-fnn r-forcats r-future r-future-apply r-gg-gap r-ggalluvial r-ggplot2 r-ggrepel r-igraph r-irlba r-magrittr r-matrix r-nmf r-patchwork r-pbapply r-rcolorbrewer r-rcpp r-rcppeigen r-reshape2 r-reticulate r-rspectra r-rtsne r-scales r-shape r-sna r-stringr r-svglite)) (native-inputs (list r-knitr)) (home-page "https://github.com/sqjin/CellChat") (synopsis "Analysis of cell-cell communication from single-cell transcriptomics data") (description "This package infers, visualizes and analyzes the cell-cell communication networks from scRNA-seq data.") (license license:gpl3)))) (define-public r-copykat (let ((commit ;no tag "256de33dfc1b80a1a0ac9e098c5557f95a4e0d53") (revision "0")) (package (name "r-copykat") (version (git-version "1.0.8" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/navinlabcode/copykat") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0ckyqnial3imcqlgd6xfgwk5w977l1i87sx4kdbwdvg40w0vh1j8")))) (properties `((upstream-name . "copykat"))) (build-system r-build-system) (propagated-inputs (list r-cluster r-dlm r-gplots r-mcmcpack r-mixtools r-paralleldist r-rcolorbrewer)) (native-inputs (list r-knitr)) (home-page "https://github.com/navinlabcode/copykat") (synopsis "Inference of genomic copy number from single cell RNAseq data") (description "This package Copynumber KAryotyping of Tumors infers genomic copy number and subclonal structure of human tumors using integrative Bayesian approaches to identify genome-wide aneuploidy at 5MB resolution in single cells data. It separates tumor cells and tumor subclones from normal cells using high-throughput sc-RNAseq data.") (license license:gpl2)))) (define-public sambamba (package (name "sambamba") (version "0.8.2") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/biod/sambamba") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "1zdkd1md5wk4la71p82pbclqqcm55abk23fk087da6186i1bsihl")))) (build-system gnu-build-system) (arguments `(#:tests? #f ; there is no test target #:parallel-build? #f ; not supported #:phases (modify-phases %standard-phases (delete 'configure) (add-after 'unpack 'prepare-build-tools (lambda* (#:key inputs #:allow-other-keys) (substitute* "Makefile" (("\\$\$shell which ldmd2\$") (which "ldmd2"))) (setenv "CC" "gcc") (setenv "D_LD" (which "ld.gold")))) (add-after 'unpack 'unbundle-prerequisites (lambda _ (substitute* "Makefile" (("= lz4/lib/liblz4.a") "= -L-llz4") (("ldc_version_info lz4-static") "ldc_version_info")))) (replace 'install (lambda* (#:key outputs #:allow-other-keys) (let ((bin (string-append (assoc-ref outputs "out") "/bin"))) (mkdir-p bin) (copy-file (string-append "bin/sambamba-" ,version) (string-append bin "/sambamba")))))))) (native-inputs (list python)) (inputs (list ldc lz4 zlib)) (home-page "https://github.com/biod/sambamba") (synopsis "Tools for working with SAM/BAM data") (description "Sambamba is a high performance modern robust and fast tool (and library), written in the D programming language, for working with SAM and BAM files. Current parallelised functionality is an important subset of samtools functionality, including view, index, sort, markdup, and depth.") (license license:gpl2+))) (define-public r-rphyloxml (let ((commit "a30e39249239b2de01d6964ae2a2205a6c48b475") (revision "1")) (package (name "r-rphyloxml") (version (git-version "0.0-9000" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/USCbiostats/rphyloxml") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "15ijzqvjxx6vqyqlg5asdbqlhw1g0ix6palf1rism3si0qapddgw")) (snippet '(delete-file "docs/jquery.sticky-kit.min.js")))) (properties `((upstream-name . "rphyloxml"))) (build-system r-build-system) (arguments (list #:modules '((guix build r-build-system) (guix build minify-build-system) (guix build utils)) #:imported-modules `(,@%r-build-system-modules (guix build minify-build-system)) #:phases '(modify-phases %standard-phases (add-after 'unpack 'process-javascript (lambda* (#:key inputs #:allow-other-keys) (with-directory-excursion "inst/" (minify (assoc-ref inputs "js-jquery-sticky-kit") #:target "docs/jquery.sticky-kit.min.js"))))))) (propagated-inputs (list r-ape r-xml2)) (native-inputs `(("esbuild" ,esbuild) ("js-jquery-sticky-kit" ,(origin (method url-fetch) (uri "https://raw.githubusercontent.com/leafo/sticky-kit/\ v1.1.2/jquery.sticky-kit.js") (sha256 (base32 "17c3a1hqc3ybwj7hpw8prazajp2x98aq7nyfn71h6lzjvblq297g")))))) (home-page "https://github.com/USCbiostats/rphyloxml") (synopsis "Read and write phyloXML files in R") (description "The package reads phylogenetic data in the @code{phyloXML} format. It also includes functions for writing data in this format.") (license license:expat)))) (define-public ritornello (package (name "ritornello") (version "2.0.1") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/KlugerLab/Ritornello") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "1xahvq215qld7x1w8vpa5zbrsj6p9crb9shqa2x89sb0aaxa02jk")))) (build-system gnu-build-system) (arguments `(#:tests? #f ; there are no tests #:phases (modify-phases %standard-phases (add-after 'unpack 'patch-samtools-references (lambda* (#:key inputs #:allow-other-keys) (substitute* '("src/SamStream.h" "src/FLD.cpp") (("<sam.h>") "<samtools/sam.h>")) #t)) (delete 'configure) (replace 'install (lambda* (#:key inputs outputs #:allow-other-keys) (let* ((out (assoc-ref outputs "out")) (bin (string-append out "/bin/"))) (mkdir-p bin) (install-file "bin/Ritornello" bin) #t)))))) (inputs (list samtools-0.1 fftw boost zlib)) (home-page "https://github.com/KlugerLab/Ritornello") (synopsis "Control-free peak caller for ChIP-seq data") (description "Ritornello is a ChIP-seq peak calling algorithm based on signal processing that can accurately call binding events without the need to do a pair total DNA input or IgG control sample. It has been tested for use with narrow binding events such as transcription factor ChIP-seq.") (license license:gpl3+))) (define-public trim-galore (package (name "trim-galore") (version "0.6.6") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/FelixKrueger/TrimGalore") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "0yrwg6325j4sb9vnplvl3jplzab0qdhp92wl480qjinpfq88j4rs")))) (build-system gnu-build-system) (arguments `(#:tests? #f ; no tests #:phases (modify-phases %standard-phases (replace 'configure (lambda _ ;; Trim Galore tries to figure out what version of Python ;; cutadapt is using by looking at the shebang. Of course that ;; doesn't work, because cutadapt is wrapped in a shell script. (substitute* "trim_galore" (("my \\$python_return.*") "my $python_return = \"Python 3.999\";\n")) #t)) (delete 'build) (add-after 'unpack 'hardcode-tool-references (lambda* (#:key inputs #:allow-other-keys) (substitute* "trim_galore" (("\\$path_to_cutadapt = 'cutadapt'") (string-append "$path_to_cutadapt = '" (assoc-ref inputs "cutadapt") "/bin/cutadapt'")) (("\\$compression_path = \"gzip\"") (string-append "$compression_path = \"" (assoc-ref inputs "gzip") "/bin/gzip\"")) (("\"gunzip") (string-append "\"" (assoc-ref inputs "gzip") "/bin/gunzip")) (("\"pigz") (string-append "\"" (assoc-ref inputs "pigz") "/bin/pigz"))) #t)) (replace 'install (lambda* (#:key outputs #:allow-other-keys) (let ((bin (string-append (assoc-ref outputs "out") "/bin"))) (mkdir-p bin) (install-file "trim_galore" bin) #t)))))) (inputs (list gzip perl pigz cutadapt)) (native-inputs (list unzip)) (home-page "https://www.bioinformatics.babraham.ac.uk/projects/trim_galore/") (synopsis "Wrapper around Cutadapt and FastQC") (description "Trim Galore! is a wrapper script to automate quality and adapter trimming as well as quality control, with some added functionality to remove biased methylation positions for RRBS sequence files.") (license license:gpl3+))) (define-public phylip (package (name "phylip") (version "3.697") (source (origin (method url-fetch) (uri (string-append "http://evolution.gs.washington.edu/phylip/" "download/phylip-" version ".tar.gz")) (sha256 (base32 "1h8h0nafnlbqryswxgplx80k2044yhfz97jh13vsgzlaifqdh9ls")))) (build-system gnu-build-system) (arguments `(#:tests? #f ; no check target #:make-flags (list "-f" "Makefile.unx" "CFLAGS=-fcommon" "install") #:parallel-build? #f ; not supported #:phases (modify-phases %standard-phases (add-after 'unpack 'enter-dir (lambda _ (chdir "src"))) (delete 'configure) (replace 'install (lambda* (#:key inputs outputs #:allow-other-keys) (let ((target (string-append (assoc-ref outputs "out") "/bin"))) (mkdir-p target) (for-each (lambda (file) (install-file file target)) (find-files "../exe" ".*")))))))) (home-page "https://evolution.genetics.washington.edu/phylip/") (synopsis "Tools for inferring phylogenies") (description "PHYLIP (the PHYLogeny Inference Package) is a package of programs for inferring phylogenies (evolutionary trees).") (license license:bsd-2))) (define-public phyml (package (name "phyml") (version "3.3.20220408") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/stephaneguindon/phyml") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "03hdqmnsgnzkcrp9r9ajdfkj33jgq4b86kra8ssjlrph65y344sa")) (snippet '(delete-file "doc/phyml-manual.pdf")))) (build-system gnu-build-system) (supported-systems '("x86_64-linux")) (arguments (let ((default-flags (list "--disable-native"))) `(#:phases (let ((build (lambda (what) (lambda args (apply (assoc-ref %standard-phases 'configure) (append args (list #:configure-flags (cons (format #false "--enable-~a" what) '() #;,default-flags)))) (apply (assoc-ref %standard-phases 'build) args) (apply (assoc-ref %standard-phases 'install) args))))) (modify-phases %standard-phases ;; We cannot use --disable-native; see ;; https://github.com/stephaneguindon/phyml/issues/173 Instead we ;; patch the code to at least get rid of -march=native. (add-after 'unpack 'remove-march-native (lambda _ (substitute* "configure.ac" (("DEFAULT_VECTOR_FLAG=\"-march=native\"") "DEFAULT_VECTOR_FLAG=\"-march=athlon64-sse3\"\n")))) (add-after 'build 'build-manual (lambda _ (with-directory-excursion "doc" (invoke "make" "phyml-manual.pdf")))) (add-after 'build-manual 'install-manual (lambda* (#:key outputs #:allow-other-keys) (with-directory-excursion "doc" (install-file "phyml-manual.pdf" (string-append (assoc-ref outputs "out") "/share/doc/phyml"))))) (add-after 'install 'build-phyml-mpi (build "phyml-mpi")) (add-after 'build-phyml-mpi 'build-rf (build "rf")) (add-after 'build-rf 'build-phyrex (build "phyrex"))))))) (native-inputs (list automake autoconf openmpi (texlive-updmap.cfg (list texlive-caption texlive-cite texlive-fancyvrb texlive-infwarerr texlive-kvoptions texlive-pdftexcmds texlive-psfrag texlive-xcolor)))) (home-page "https://github.com/stephaneguindon/phyml") (synopsis "Programs for working on SAM/BAM files") (description "@code{PhyML} is a software package that uses modern statistical approaches to analyse alignments of nucleotide or amino acid sequences in a phylogenetic framework. The main tool in this package builds phylogenies under the maximum likelihood criterion. It implements a large number of substitution models coupled with efficient options to search the space of phylogenetic tree topologies. code{PhyREX} fits the spatial-Lambda-Fleming-Viot model to geo-referenced genetic data. This model is similar to the structured coalescent but assumes that individuals are distributed along a spatial continuum rather than discrete demes. @code{PhyREX} can be used to estimate population densities and rates of dispersal. Its output can be processed by treeannotator (from the @code{BEAST} package) as well as @code{SPREAD}.") (license license:gpl3))) (define-public imp (package (name "imp") (version "2.15.0") (source (origin (method url-fetch) (uri (string-append "https://integrativemodeling.org/" version "/download/imp-" version ".tar.gz")) (sha256 (base32 "05hsrnkpkajppa3f45x4qsarnkj616hlby749zxg4is3bv4i6b5y")))) (build-system cmake-build-system) (arguments `(#:tests? #false ; The test suite is notoriously fickle #:configure-flags (let ((disabled-tests '("expensive" ;exclude expensive tests "IMP.modeller" ;fail to import its own modules "IMP.parallel-test_sge.py" ;fail in build container ;; The following test fails non-reproducibly on ;; an inexact numbers assertion. "IMP.em-medium_test_local_fitting.py" ;; The following test fails for unknown reasons "IMP.foxs-add-missing-residues.py"))) (list (string-append "-DCMAKE_CTEST_ARGUMENTS=" (string-join (list "-L" "-tests?-" ;select only tests "-E" (format #f "'(~a)'" (string-join disabled-tests "|"))) ";")))))) (native-inputs `(("python" ,python-wrapper) ("swig" ,swig))) (inputs (list boost cgal gsl hdf5 fftw eigen ;; Enabling MPI causes the build to use all the available memory and ;; fail (tested on a machine with 32 GiB of RAM). ;;("mpi" ,openmpi) opencv)) (propagated-inputs (list python-numpy python-scipy python-pandas python-scikit-learn python-networkx)) (home-page "https://integrativemodeling.org") (synopsis "Integrative modeling platform") (description "IMP's broad goal is to contribute to a comprehensive structural characterization of biomolecules ranging in size and complexity from small peptides to large macromolecular assemblies, by integrating data from diverse biochemical and biophysical experiments. IMP provides a C++ and Python toolbox for solving complex modeling problems, and a number of applications for tackling some common problems in a user-friendly way.") ;; IMP is largely available under the GNU Lesser GPL; see the file ;; COPYING.LGPL for the full text of this license. Some IMP modules are ;; available under the GNU GPL (see the file COPYING.GPL). (license (list license:lgpl2.1+ license:gpl3+)))) ;; We use this seemingly arbitrary commit because of ;; https://github.com/3DGenomes/TADbit/issues/371 (define-public tadbit (let ((commit "283812901a00078c725bd9f0ee33366af6783969") (revision "2")) (package (name "tadbit") (version (git-version "1.0.1" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/3DGenomes/TADbit") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "07q0alxah6xl1hibaj1kj7pdzq3pg6csyapsihbwlbmqyfmllbgz")))) (build-system python-build-system) (arguments (list #:phases #~(modify-phases %standard-phases ;; Scipy 1.12 no longer has binom_test or polyfit (add-after 'unpack 'scipy-compatibility (lambda _ (substitute* '("_pytadbit/modelling/imp_modelling.py" "_pytadbit/modelling/restraints.py") (("from scipy .*import polyfit") "from numpy import polyfit")) (substitute* "_pytadbit/mapping/restriction_enzymes.py" (("from scipy.stats import binom_test") "from scipy.stats import binomtest") (("binom_test\$pats[k]['count'], nreads, 0.25\\*\\*len\\(k\$, alternative='greater'\\)") "binomtest(pats[k]['count'], nreads, 0.25**len(k), alternative='greater').pval")))) (add-after 'unpack 'fix-problems-with-setup.py (lambda _ (substitute* "src/test/Makefile" (("^CFLAGS=") "CFLAGS= -fcommon")) ;; Don't attempt to install the bash completions to ;; the home directory. (rename-file "extras/.bash_completion" "extras/tadbit") (substitute* "setup.py" (("\$path.expanduser\\('~'\$") (string-append "(\"" #$output "/etc/bash_completion.d\"")) (("extras/\\.bash_completion") "extras/tadbit")))) (replace 'check (lambda* (#:key tests? #:allow-other-keys) (when tests? (invoke "python3" "test/test_all.py"))))))) (native-inputs (list `(,glib "bin") ;for gtester glib pkg-config)) (inputs ;; TODO: add Chimera for visualization (list imp mcl python-future python-h5py python-scipy python-numpy python-matplotlib python-pysam r-minimal)) (home-page "https://3dgenomes.github.io/TADbit/") (synopsis "Analyze, model, and explore 3C-based data") (description "TADbit is a complete Python library to deal with all steps to analyze, model, and explore 3C-based data. With TADbit the user can map FASTQ files to obtain raw interaction binned matrices (Hi-C like matrices), normalize and correct interaction matrices, identify and compare the so-called @dfn{Topologically Associating Domains} (TADs), build 3D models from the interaction matrices, and finally, extract structural properties from the models. TADbit is complemented by TADkit for visualizing 3D models.") (license license:gpl3+)))) (define-public kentutils (package (name "kentutils") ;; 302.1.0 is out, but the only difference is the inclusion of ;; pre-built binaries. (version "302.0.0") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/ENCODE-DCC/kentUtils") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "0n1wbyjpzii2b9qhyp9r1q76j623cggpg3y8fmw78ld3z4y7ivha")) (modules '((guix build utils) (srfi srfi-26) (ice-9 ftw))) (snippet '(begin ;; Only the contents of the specified directories are free ;; for all uses, so we remove the rest. "hg/autoSql" and ;; "hg/autoXml" are nominally free, but they depend on a ;; library that is built from the sources in "hg/lib", ;; which is nonfree. (let ((free (list "." ".." "utils" "lib" "inc" "tagStorm" "parasol" "htslib")) (directory? (lambda (file) (eq? 'directory (stat:type (stat file)))))) (for-each (lambda (file) (and (directory? file) (delete-file-recursively file))) (map (cut string-append "src/" <>) (scandir "src" (lambda (file) (not (member file free))))))) ;; Only make the utils target, not the userApps target, ;; because that requires libraries we won't build. (substitute* "Makefile" ((" userApps") " utils")) ;; Only build libraries that are free. (substitute* "src/makefile" (("DIRS =.*") "DIRS =\n") (("cd jkOwnLib.*") "") ((" hgLib") "") (("cd hg.*") "")) (substitute* "src/utils/makefile" ;; These tools depend on "jkhgap.a", which is part of the ;; nonfree "src/hg/lib" directory. (("raSqlQuery") "") (("pslLiftSubrangeBlat") "") ;; Do not build UCSC tools, which may require nonfree ;; components. (("ALL_APPS =.*") "ALL_APPS = $(UTILS_APPLIST)\n")) #t)))) (build-system gnu-build-system) (arguments `( ;; There is no global test target and the test target for ;; individual tools depends on input files that are not ;; included. #:tests? #f #:phases (modify-phases %standard-phases (add-after 'unpack 'fix-permissions (lambda _ (make-file-writable "src/inc/localEnvironment.mk") #t)) (add-after 'unpack 'fix-paths (lambda _ (substitute* "Makefile" (("/bin/echo") (which "echo"))) #t)) (add-after 'unpack 'prepare-samtabix (lambda* (#:key inputs #:allow-other-keys) (copy-recursively (assoc-ref inputs "samtabix") "samtabix") #t)) (delete 'configure) (replace 'install (lambda* (#:key outputs #:allow-other-keys) (let ((bin (string-append (assoc-ref outputs "out") "/bin"))) (copy-recursively "bin" bin)) #t))))) (native-inputs `(("samtabix" ,(let ((commit "10fd107909c1ac4d679299908be4262a012965ba")) (origin (method git-fetch) (uri (git-reference (url "http://genome-source.cse.ucsc.edu/samtabix.git") (commit commit))) (file-name (git-file-name "samtabix" (string-take commit 7))) (sha256 (base32 "0c1nj64l42v395sa84n7az43xiap4i6f9n9dfz4058aqiwkhkmma"))))))) (inputs `(("zlib" ,zlib) ("tcsh" ,tcsh) ("perl" ,perl) ("libpng" ,libpng) ("mariadb-dev" ,mariadb "dev") ("openssl" ,openssl))) (home-page "https://genome.cse.ucsc.edu/index.html") (synopsis "Assorted bioinformatics utilities") (description "This package provides the kentUtils, a selection of bioinformatics utilities used in combination with the UCSC genome browser.") ;; Only a subset of the sources are released under a non-copyleft ;; free software license. All other sources are removed in a ;; snippet. See this bug report for an explanation of how the ;; license statements apply: ;; https://github.com/ENCODE-DCC/kentUtils/issues/12 (license (license:non-copyleft "http://genome.ucsc.edu/license/" "The contents of this package are free for all uses.")))) (define-public f-seq (let ((commit "6ccded34cff38cf432deed8503648b4a66953f9b") (revision "1")) (package (name "f-seq") (version (git-version "1.1" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/aboyle/F-seq") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "1nk33k0yajg2id4g59bc4szr58r2q6pdq42vgcw054m8ip9wv26h")) (modules '((guix build utils))) ;; Remove bundled Java library archives. (snippet '(for-each delete-file (find-files "lib" ".*"))))) (build-system ant-build-system) (arguments `(#:tests? #f ; no tests included #:phases (modify-phases %standard-phases (replace 'install (lambda* (#:key inputs outputs #:allow-other-keys) (let* ((target (assoc-ref outputs "out")) (bin (string-append target "/bin")) (doc (string-append target "/share/doc/f-seq")) (lib (string-append target "/lib"))) (mkdir-p target) (mkdir-p doc) (substitute* "bin/linux/fseq" (("java") (which "java")) (("\\$REALDIR/../lib/commons-cli-1.1.jar") (search-input-file inputs (string-append "/lib/m2/commons-cli/commons-cli/" ,(package-version java-commons-cli) "/commons-cli-" ,(package-version java-commons-cli) ".jar"))) (("REALDIR=.*") (string-append "REALDIR=" bin "\n"))) (install-file "README.txt" doc) (install-file "bin/linux/fseq" bin) (install-file "build~/fseq.jar" lib) (copy-recursively "lib" lib))))))) (inputs (list perl java-commons-cli)) (home-page "https://fureylab.web.unc.edu/software/fseq/") (synopsis "Feature density estimator for high-throughput sequence tags") (description "F-Seq is a software package that generates a continuous tag sequence density estimation allowing identification of biologically meaningful sites such as transcription factor binding sites (ChIP-seq) or regions of open chromatin (DNase-seq). Output can be displayed directly in the UCSC Genome Browser.") (license license:gpl3+)))) (define-public bismark (package (name "bismark") (version "0.24.1") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/FelixKrueger/Bismark") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "0j4dy33769f0jr2w1brb710zxwpg3zwjlnvlcpi5pr6mqc8dkg8n")) (snippet '(delete-file "plotly/plot.ly")))) (build-system perl-build-system) (arguments (list #:tests? #f ; there are no tests #:modules '((guix build utils) (ice-9 popen) (srfi srfi-26) (guix build perl-build-system)) #:phases #~(modify-phases %standard-phases (add-after 'unpack 'replace-plotly.js (lambda* (#:key inputs #:allow-other-keys) (let* ((share (string-append #$output "/share/bismark")) (file (assoc-ref inputs "plotly.js")) (installed "plotly/plotly.js")) ;; The bundled plotly.js is minified. (let ((minified (open-pipe* OPEN_READ "uglifyjs" file))) (call-with-output-file installed (cut dump-port minified <>))) (substitute* "bismark2report" (("plotly_template.tpl") (string-append share "/plotly/plotly_template.tpl")) (("my \\$plotly_code = read_report_template\$'plot.ly'\$;") (string-append "\ my $plotly_code = read_report_template('" share "/plotly/plotly.js'); $plotly_code = \"<script>\" . $plotly_code . \"</script>\";")))))) (replace 'configure (lambda* (#:key inputs #:allow-other-keys) (substitute* "bismark" (("\$\\!system \"which samtools >/dev/null 2>&1\"\$") "(\"true\")") (("\\$samtools_path = `which samtools`;") (string-append "$samtools_path = '" (search-input-file inputs "/bin/samtools") "';")) (("\\$path_to_bowtie2 = 'bowtie2'") (string-append "$path_to_bowtie2 = '" (search-input-file inputs "/bin/bowtie2") "'")) (("\\$path_to_hisat2 = 'hisat2'") (string-append "$path_to_hisat2 = '" (search-input-file inputs "/bin/hisat2") "'")) (("\\$path_to_minimap2 = 'minimap2'") (string-append "$path_to_minimap2 = '" (search-input-file inputs "/bin/minimap2") "'"))))) (delete 'build) (replace 'install (lambda* (#:key inputs outputs #:allow-other-keys) (let* ((bin (string-append #$output "/bin")) (share (string-append #$output "/share/bismark")) (docdir (string-append #$output "/share/doc/bismark")) (scripts '("bismark" "bismark_genome_preparation" "bismark_methylation_extractor" "bismark2bedGraph" "bismark2report" "coverage2cytosine" "deduplicate_bismark" "filter_non_conversion" "bam2nuc" "bismark2summary" "NOMe_filtering"))) (mkdir-p share) (mkdir-p docdir) (mkdir-p bin) (for-each (lambda (file) (install-file file bin)) scripts) (copy-recursively "docs" docdir) (copy-recursively "plotly" (string-append share "/plotly")) ;; Fix references to gunzip (substitute* (map (lambda (file) (string-append bin "/" file)) scripts) (("\"gunzip -c") (string-append "\"" (assoc-ref inputs "gzip") "/bin/gunzip -c"))))))))) (inputs (list bowtie gzip hisat2 minimap2 perl-carp perl-getopt-long samtools)) (native-inputs `(("plotly.js" ,(origin (method url-fetch) (uri (string-append "https://raw.githubusercontent.com/plotly/plotly.js/" "v1.39.4/dist/plotly.js")) (sha256 (base32 "138mwsr4nf5qif4mrxx286mpnagxd1xwl6k8aidrjgknaqg88zyr")))) ("uglifyjs" ,node-uglify-js))) (home-page "https://www.bioinformatics.babraham.ac.uk/projects/bismark/") (synopsis "Map bisulfite treated sequence reads and analyze methylation") (description "Bismark is a program to map bisulfite treated sequencing reads to a genome of interest and perform methylation calls in a single step. The output can be easily imported into a genome viewer, such as SeqMonk, and enables a researcher to analyse the methylation levels of their samples straight away. Its main features are: @itemize @item Bisulfite mapping and methylation calling in one single step @item Supports single-end and paired-end read alignments @item Supports ungapped and gapped alignments @item Alignment seed length, number of mismatches etc are adjustable @item Output discriminates between cytosine methylation in CpG, CHG and CHH context @end itemize\n") (license license:gpl3+))) (define-public paml (package (name "paml") (version "4.9e") (source (origin (method url-fetch) (uri (string-append "http://abacus.gene.ucl.ac.uk/software/" "paml" version ".tgz")) (sha256 (base32 "13zf6h9fiqghwhch2h06x1zdr6s42plsnqahflp5g7myr3han3s6")) (modules '((guix build utils))) ;; Remove Windows binaries (snippet '(begin (for-each delete-file (find-files "." "\\.exe$")) ;; Some files in the original tarball have restrictive ;; permissions, which makes repackaging fail (for-each (lambda (file) (chmod file #o644)) (find-files ".")) #t)))) (build-system gnu-build-system) (arguments `(#:tests? #f ; there are no tests #:make-flags '("CC=gcc" "CFLAGS=-fcommon -O3") #:phases (modify-phases %standard-phases (replace 'configure (lambda _ (substitute* "src/BFdriver.c" (("/bin/bash") (which "bash"))) (chdir "src"))) (replace 'install (lambda* (#:key outputs #:allow-other-keys) (let ((tools '("baseml" "basemlg" "codeml" "pamp" "evolver" "yn00" "chi2")) (bin (string-append (assoc-ref outputs "out") "/bin")) (docdir (string-append (assoc-ref outputs "out") "/share/doc/paml"))) (mkdir-p bin) (for-each (lambda (file) (install-file file bin)) tools) (copy-recursively "../doc" docdir))))))) (home-page "http://abacus.gene.ucl.ac.uk/software/paml.html") (synopsis "Phylogentic analysis by maximum likelihood") (description "PAML (for Phylogentic Analysis by Maximum Likelihood) contains a few programs for model fitting and phylogenetic tree reconstruction using nucleotide or amino-acid sequence data.") ;; GPLv3 only (license license:gpl3))) (define-public segemehl (package (name "segemehl") (version "0.3.4") (source (origin (method url-fetch) (uri (string-append "https://www.bioinf.uni-leipzig.de/Software" "/segemehl/downloads/segemehl-" version ".tar.gz")) (sha256 (base32 "0lbzbb7i8zadsn9b99plairhq6s2h1z8qdn6n7djclfis01nycz4")))) (build-system gnu-build-system) (arguments `(#:make-flags (list (string-append "CC=" ,(cc-for-target)) "all") #:tests? #false ; there are none #:phases (modify-phases %standard-phases (delete 'configure) ;; There is no installation target (replace 'install (lambda* (#:key inputs outputs #:allow-other-keys) (let* ((out (assoc-ref outputs "out")) (bin (string-append out "/bin")) (exes (list "segemehl.x" "haarz.x"))) (mkdir-p bin) (for-each (lambda (exe) (install-file exe bin)) exes))))))) (inputs (list htslib ncurses zlib)) (native-inputs (list pkg-config)) (home-page "https://www.bioinf.uni-leipzig.de/Software/segemehl") (synopsis "Map short sequencer reads to reference genomes") (description "Segemehl is software to map short sequencer reads to reference genomes. Segemehl implements a matching strategy based on enhanced suffix arrays (ESA). It accepts fasta and fastq queries (gzip'ed and bgzip'ed). In addition to the alignment of reads from standard DNA- and RNA-seq protocols, it also allows the mapping of bisulfite converted reads (Lister and Cokus) and implements a split read mapping strategy. The output of segemehl is a SAM or BAM formatted alignment file.") (license license:gpl3+))) (define-public kallisto (package (name "kallisto") (version "0.48.0") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/pachterlab/kallisto") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "0wx1ndmhndsd60952piaa925lk8bjr59d2yr1m2hcsqcb6cdjwpn")) (modules '((guix build utils))) (snippet '(delete-file-recursively "ext/htslib/")))) (build-system cmake-build-system) (arguments `(#:tests? #f ; no "check" target #:phases (modify-phases %standard-phases (add-after 'unpack 'do-not-use-bundled-htslib (lambda _ (substitute* "CMakeLists.txt" (("^ExternalProject_Add" m) (string-append "if (NEVER)\n" m)) (("^\\)") (string-append ")\nendif(NEVER)")) (("include_directories\$\\$\\{htslib_PREFIX.*" m) (string-append "# " m))) (substitute* "src/CMakeLists.txt" (("target_link_libraries\\(kallisto kallisto_core pthread \ \\$\\{CMAKE_CURRENT_SOURCE_DIR\\}/../ext/htslib/libhts.a\$") "target_link_libraries(kallisto kallisto_core pthread hts)") (("include_directories\$\\.\\./ext/htslib\$") ""))))))) (inputs (list hdf5 htslib-1.9 zlib)) (home-page "https://pachterlab.github.io/kallisto/") (synopsis "Near-optimal RNA-Seq quantification") (description "Kallisto is a program for quantifying abundances of transcripts from RNA-Seq data, or more generally of target sequences using high-throughput sequencing reads. It is based on the novel idea of pseudoalignment for rapidly determining the compatibility of reads with targets, without the need for alignment. Pseudoalignment of reads preserves the key information needed for quantification, and kallisto is therefore not only fast, but also as accurate as existing quantification tools.") (license license:bsd-2))) (define-public libgff (package (name "libgff") (version "2.0.0") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/COMBINE-lab/libgff") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "0ds9r22y8bl1rj7bhl0003kgmm6aam7g8l41mnjfrzw15d9zf9k4")))) (build-system cmake-build-system) (arguments `(#:tests? #f)) ; no tests included (home-page "https://github.com/COMBINE-lab/libgff") (synopsis "Parser library for reading/writing GFF files") (description "This is a simple \"libraryfication\" of the GFF/GTF parsing code that is used in the Cufflinks codebase. The goal of this library is to provide this functionality without the necessity of drawing in a heavy-weight dependency like SeqAn.") (license (license:x11-style "https://www.boost.org/LICENSE_1_0.txt")))) (define-public sailfish (package (name "sailfish") (version "0.10.1") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/kingsfordgroup/sailfish") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "1amcc5hqvsl42hg4x19bi9vy47cl874s0lw1fmi0hwsdk9i8c03v")) (modules '((guix build utils))) ;; Delete bundled headers for eigen3. (snippet '(delete-file-recursively "include/eigen3/")))) (build-system cmake-build-system) (arguments `(#:configure-flags ,#~(list (string-append "-DBOOST_INCLUDEDIR=" #$(this-package-input "boost") "/include/") (string-append "-DBOOST_LIBRARYDIR=" #$(this-package-input "boost") "/lib/") (string-append "-DBoost_LIBRARIES=" "-lboost_iostreams " "-lboost_filesystem " "-lboost_system " "-lboost_thread " "-lboost_timer " "-lboost_chrono " "-lboost_program_options") "-DBoost_FOUND=TRUE" ;; Don't download RapMap---we already have it! "-DFETCHED_RAPMAP=1") ;; Tests must be run after installation and the location of the test ;; data file must be overridden. But the tests fail. It looks like ;; they are not really meant to be run. #:tests? #f #:phases (modify-phases %standard-phases ;; Boost cannot be found, even though it's right there. (add-after 'unpack 'do-not-look-for-boost (lambda* (#:key inputs #:allow-other-keys) (substitute* "CMakeLists.txt" (("find_package\\(Boost 1\\.53\\.0") "#")))) (add-after 'unpack 'do-not-assign-to-macro (lambda _ (substitute* "include/spdlog/details/format.cc" (("const unsigned CHAR_WIDTH = 1;") "")))) (add-after 'unpack 'prepare-rapmap (lambda* (#:key inputs #:allow-other-keys) (let ((src "external/install/src/rapmap/") (include "external/install/include/rapmap/") (rapmap (assoc-ref inputs "rapmap"))) (mkdir-p src) (mkdir-p include) (for-each (lambda (file) (install-file file src)) (find-files (string-append rapmap "/src") "\\.(c|cpp)")) (copy-recursively (string-append rapmap "/include") include)))) (add-after 'unpack 'use-system-libraries (lambda* (#:key inputs #:allow-other-keys) (substitute* '("src/SailfishIndexer.cpp" "src/SailfishUtils.cpp" "src/SailfishQuantify.cpp" "src/FASTAParser.cpp" "include/PCA.hpp" "include/SailfishUtils.hpp" "include/SailfishIndex.hpp" "include/CollapsedEMOptimizer.hpp" "src/CollapsedEMOptimizer.cpp") (("#include \"jellyfish/config.h\"") "")) (substitute* "src/CMakeLists.txt" (("\\$\\{GAT_SOURCE_DIR\\}/external/install/include/jellyfish-2.2..") (search-input-directory inputs (string-append "/include/jellyfish-" ,(package-version jellyfish)))) (("\\$\\{GAT_SOURCE_DIR\\}/external/install/lib/libjellyfish-2.0.a") (search-input-file inputs "/lib/libjellyfish-2.0.a")) (("\\$\\{GAT_SOURCE_DIR\\}/external/install/lib/libdivsufsort.a") (search-input-file inputs "/lib/libdivsufsort.so")) (("\\$\\{GAT_SOURCE_DIR\\}/external/install/lib/libdivsufsort64.a") (search-input-file inputs "/lib/libdivsufsort64.so"))) (substitute* "CMakeLists.txt" ;; Don't prefer static libs (("SET\\(CMAKE_FIND_LIBRARY_SUFFIXES.*") "") (("find_package\\(Jellyfish.*") "") (("ExternalProject_Add\\(libjellyfish") "message(") (("ExternalProject_Add\\(libgff") "message(") (("ExternalProject_Add\\(libsparsehash") "message(") (("ExternalProject_Add\\(libdivsufsort") "message(")) ;; Ensure that Eigen headers can be found (setenv "CPLUS_INCLUDE_PATH" (string-append (search-input-directory inputs "/include/eigen3") ":" (or (getenv "CPLUS_INCLUDE_PATH") "")))))))) (inputs `(("boost" ,boost) ("eigen" ,eigen) ("jemalloc" ,jemalloc) ("jellyfish" ,jellyfish) ("sparsehash" ,sparsehash) ("rapmap" ,(origin (method git-fetch) (uri (git-reference (url "https://github.com/COMBINE-lab/RapMap") (commit (string-append "sf-v" version)))) (file-name (string-append "rapmap-sf-v" version "-checkout")) (sha256 (base32 "1hv79l5i576ykv5a1srj2p0q36yvyl5966m0fcy2lbi169ipjakf")) (modules '((guix build utils))) ;; These files are expected to be excluded. (snippet '(begin (delete-file-recursively "include/spdlog") (for-each delete-file '("include/xxhash.h" "src/xxhash.c")))))) ("libdivsufsort" ,libdivsufsort) ("libgff" ,libgff) ("tbb" ,tbb-2020) ("zlib" ,zlib))) (native-inputs (list pkg-config)) (home-page "https://www.cs.cmu.edu/~ckingsf/software/sailfish/") (synopsis "Mapping-based isoform quantification from RNA-Seq reads") (description "Sailfish is a tool for genomic transcript quantification from RNA-seq data. It requires a set of target transcripts (either from a reference or de-novo assembly) to quantify. All you need to run sailfish is a fasta file containing your reference transcripts and a (set of) fasta/fastq file(s) containing your reads.") (license license:gpl3+))) (define libstadenio-for-salmon (package (name "libstadenio") (version "1.14.8") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/COMBINE-lab/staden-io_lib") (commit (string-append "v" version)))) (file-name (string-append name "-" version "-checkout")) (sha256 (base32 "1x8kxxqxl892vwfbprlbyfwkkv7c34ggkc94892x9x0g37x5nbwx")))) (build-system gnu-build-system) (arguments '(#:parallel-tests? #f)) ; not supported (inputs `(("zlib" ,zlib))) (native-inputs `(("perl" ,perl))) ; for tests (home-page "https://github.com/COMBINE-lab/staden-io_lib") (synopsis "General purpose trace and experiment file library") (description "This package provides a library of file reading and writing code to provide a general purpose Trace file (and Experiment File) reading interface. The following file formats are supported: @enumerate @item SCF trace files @item ABI trace files @item ALF trace files @item ZTR trace files @item SFF trace archives @item SRF trace archives @item Experiment files @item Plain text files @item SAM/BAM sequence files @item CRAM sequence files @end enumerate\n") (license license:bsd-3))) (define-public salmon (package (name "salmon") (version "1.10.1") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/COMBINE-lab/salmon") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "0grpcajxf2bch4b74zb66pdssda8yc7jvxj5ckaw0xvw1605rpcj")) (modules '((guix build utils))) (snippet ;; Delete bundled headers for eigen3. '(delete-file-recursively "include/eigen3/")))) (build-system cmake-build-system) (arguments (list #:configure-flags #~(list (string-append "-Dlibgff_DIR=" #$(this-package-input "libgff") "/lib") "-DCMAKE_CXX_FLAGS=\"-DHAVE_NUMERIC_LIMITS128=1\"" "-Dlibgff_FOUND=TRUE" "-DTBB_FOUND=TRUE" #$(string-append "-DTBB_VERSION=" (package-version tbb)) "-DFETCHED_PUFFERFISH=TRUE" "-DUSE_SHARED_LIBS=TRUE") #:phases '(modify-phases %standard-phases (add-after 'unpack 'prepare-pufferfish (lambda* (#:key inputs #:allow-other-keys) (copy-recursively (assoc-ref inputs "pufferfish") "external/pufferfish") ;; This test isn't working correctly, so compilation aborts. (substitute* "external/pufferfish/include/string_view.hpp" (("#if __has_include\$<string_view>\$") "#if 0")) (let ((headers "external/install/pufferfish/include/pufferfish") (source "external/install/src/pufferfish")) (mkdir-p headers) (mkdir-p source) (for-each (lambda (file) (install-file (string-append "external/pufferfish/include/" file) headers)) (list "ProgOpts.hpp" "BooPHF.hpp" "SpinLock.hpp" "Kmer.hpp" "CanonicalKmer.hpp" "string_view.hpp" "CanonicalKmerIterator.hpp" "PufferfishBaseIndex.hpp" "PufferfishIndex.hpp" "PufferfishSparseIndex.hpp" "PufferfishLossyIndex.hpp" "PufferfishTypes.hpp" "rank9b.hpp" "rank9sel.hpp" "macros.hpp" "select.hpp" "Util.hpp" "PairedAlignmentFormatter.hpp" "SelectiveAlignmentUtils.hpp" "PuffAligner.hpp" "MemCollector.hpp" "MemChainer.hpp" "CommonTypes.hpp" "SAMWriter.hpp" "PufferfishConfig.hpp" "BulkChunk.hpp" "BinWriter.hpp")) (for-each (lambda (dir) (copy-recursively (string-append "external/pufferfish/include/" dir) (string-append headers "/" dir))) (list "libdivide" "ksw2pp" "compact_vector" "itlib" "metro" "chobo" "sparsepp" "simde" "tsl")) (copy-recursively (string-append "external/pufferfish/src/metro/") (string-append source "/metro")) (install-file (string-append "external/pufferfish/src/rank9b.cpp") source) ;; Do not complain about not having built libtbb (substitute* "external/pufferfish/external/twopaco/CMakeLists.txt" (("add_dependencies.*") ""))))) (add-after 'unpack 'do-not-phone-home (lambda _ (substitute* "src/Salmon.cpp" (("getVersionMessage\$\$") "\"\"")))) (add-after 'unpack 'use-system-libraries (lambda* (#:key inputs #:allow-other-keys) ;; Ensure that all headers can be found (setenv "CPLUS_INCLUDE_PATH" (string-append (or (getenv "CPLUS_INCLUDE_PATH") "") ":" (getcwd) "/external/install/pufferfish/include:" (assoc-ref inputs "eigen") "/include/eigen3")))) (add-after 'unpack 'fix-error-message-in-tests (lambda _ (substitute* "cmake/TestSalmonQuasi.cmake" (("SALMON_QUASI_INDEX_COMMAND") "SALMON_QUASI_INDEX_CMD"))))))) (inputs (list boost bzip2 cereal curl eigen htscodecs jemalloc libgff tbb libstadenio-for-salmon xz zlib)) (native-inputs `(("pkg-config" ,pkg-config) ("pufferfish" ,(origin (method git-fetch) (uri (git-reference (url "https://github.com/COMBINE-lab/pufferfish") (commit (string-append "salmon-v" version)))) (file-name (git-file-name "pufferfish" version)) (sha256 (base32 "0fcv5rd2k4fabsg489sjfxgjisivhwk1w26gfc88rgpszdkcla36")))))) (home-page "https://github.com/COMBINE-lab/salmon") (synopsis "Quantification from RNA-seq reads using lightweight alignments") (description "Salmon is a program to produce highly-accurate, transcript-level quantification estimates from RNA-seq data. Salmon achieves its accuracy and speed via a number of different innovations, including the use of lightweight alignments (accurate but fast-to-compute proxies for traditional read alignments) and massively-parallel stochastic collapsed variational inference.") (license license:gpl3+))) (define-public scallop (package (name "scallop") (version "0.10.5") (source (origin (method url-fetch) (uri (string-append "https://github.com/Kingsford-Group/scallop" "/releases/download/v" version "/scallop-" version ".tar.gz")) (sha256 (base32 "0ylkhr5hsmw7bsdszrjz9yqknsijh2fl5n6rjqmdmcdky5hkr7mh")))) (build-system gnu-build-system) (inputs (list boost htslib)) (home-page "https://github.com/Kingsford-Group/scallop") (synopsis "Reference-based transcriptome assembler for RNA-seq") (description "Scallop is a reference-based transcript assembler. Scallop features its high accuracy in assembling multi-exon transcripts as well as lowly expressed transcripts.") (license license:bsd-3))) (define-public python-fanc (package (name "python-fanc") (version "0.9.25") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/vaquerizaslab/fanc") ;; There are no tags. This commit corresponds to ;; version 0.9.25. (commit "e2205346c13ea5349681dff21adeb271d4ea5261"))) (file-name (git-file-name name version)) (sha256 (base32 "0rxq24p852iiayi0083fyigvc30as695rha71q6xd4s2ij1k9mqi")))) (build-system pyproject-build-system) (arguments (list #:phases '(modify-phases %standard-phases (replace 'check (lambda* (#:key tests? #:allow-other-keys) (when tests? (invoke "pytest" "-vv" "-k" ;; XXX: These all fail because they fail to read ;; the included test_{cooler,juicer}.hic files. (string-append "not test_edges_iter" " and not test_get_edges_uncorrected" " and not test_get_edges")))))))) (propagated-inputs (list python-biopython python-cooler python-deprecated python-future python-genomic-regions python-gridmap python-h5py python-intervaltree python-matplotlib python-msgpack python-msgpack-numpy python-numpy python-pandas python-pillow python-progressbar2 python-pybedtools python-pybigwig python-pysam python-pytest python-pyyaml python-scikit-image python-scikit-learn python-scipy python-seaborn python-tables)) (native-inputs (list python-cython)) (home-page "https://github.com/vaquerizaslab/fanc") (synopsis "Framework for the analysis of C-data") (description "FAN-C provides a pipeline for analysing Hi-C data starting at mapped paired-end sequencing reads.") (license license:gpl3+))) (define-public python-genomic-regions (package (name "python-genomic-regions") (version "0.0.10") (source (origin (method url-fetch) (uri (pypi-uri "genomic_regions" version)) (sha256 (base32 "0hz811iyd1prml1r90qyzimmwyjwycwkjqw4vnl12bxy61rfzjz5")))) (build-system pyproject-build-system) (propagated-inputs (list python-future python-intervaltree python-numpy python-pandas python-pybedtools python-pybigwig python-pytest python-msgpack-numpy python-cython python-msgpack python-pysam)) (home-page "https://pypi.org/project/genomic-regions/") (synopsis "Consistently handle genomic regions") (description "This package aims to simplify working with genomic region / interval data by providing a common interface that lets you access a wide selection of file types and formats for handling genomic region data---all using the same syntax.") (license license:expat))) (define-public python-goatools (package (name "python-goatools") (version "1.3.1") ;; Pypi tarball doesn't include test files. (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/tanghaibao/goatools") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "0a295zk9jc8kny5vnka63q3gbksins42kcmgvskf8xy7hkca7cmq")))) (build-system pyproject-build-system) (arguments (list ;; Almost all tests require access to the internet. #:tests? #false #:test-flags ;; These have syntax errors. '(list "--ignore=tests/test_i195_sgd_gaf.py" "--ignore=tests/test_i206.py" "--ignore=tests/test_setup_dirs.py"))) (propagated-inputs (list python-docopt python-numpy python-openpyxl python-pandas python-pydot python-requests python-scipy python-statsmodels python-xlsxwriter)) (native-inputs (list python-pytest)) (home-page "https://github.com/tanghaibao/goatools") (synopsis "Python scripts to find enrichment of GO terms") (description "Python scripts to find enrichment of GO terms. In addition, this package is used for processing the obo-formatted file from Gene Ontology website. The data structure is a directed acyclic graph that allows easy traversal from leaf to root.") (license license:bsd-2))) (define-public python-loompy (package (name "python-loompy") (version "3.0.7") ;; The tarball on Pypi does not include the tests. (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/linnarsson-lab/loompy") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "0xmw2yv1y3y7vh5jcbrmlkn43nmfs0pf6z78k1yxqs3qy248m9b0")))) (build-system python-build-system) (arguments `(#:phases (modify-phases %standard-phases ;; See https://github.com/linnarsson-lab/loompy/issues/169 (add-after 'unpack 'fix-h5py-error (lambda _ (substitute* "tests/test_file_attribute_manager.py" (("h5py.File\$f.name\$") "h5py.File(f.name, 'a')")))) ;; Numba needs a writable dir to cache functions. (add-before 'check 'set-numba-cache-dir (lambda _ (setenv "NUMBA_CACHE_DIR" "/tmp"))) (replace 'check (lambda* (#:key tests? #:allow-other-keys) (when tests? (invoke "pytest" "tests"))))))) (propagated-inputs (list python-click python-h5py python-numba python-numpy python-numpy-groupies python-pandas python-scipy)) (native-inputs (list python-pytest)) (home-page "https://github.com/linnarsson-lab/loompy") (synopsis "Work with .loom files for single-cell RNA-seq data") (description "The loom file format is an efficient format for very large omics datasets, consisting of a main matrix, optional additional layers, a variable number of row and column annotations. Loom also supports sparse graphs. This library makes it easy to work with @file{.loom} files for single-cell RNA-seq data.") (license license:bsd-3))) (define-public python-biothings-client (package (name "python-biothings-client") (version "0.2.6") (source (origin (method url-fetch) (uri (pypi-uri "biothings_client" version)) (sha256 (base32 "0bccs37d5saxn5xsd2rfpkrnc5a120xs3ibizai66fgvp1vxbnc4")))) (build-system python-build-system) (arguments `(#:tests? #false)) ; require internet access (propagated-inputs (list python-requests)) (home-page "https://github.com/biothings/biothings_client.py") (synopsis "Python client for BioThings API services") (description "This package provides a Python client for BioThings API services.") (license license:bsd-3))) (define-public python-mgatk (package (name "python-mgatk") (version "0.6.7") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/caleblareau/mgatk") ;; There is no tag for 0.6.7, but this is the commit ;; corresponding to the version bump. (commit "2633903acb1fb406bb58c787f320c3641f446ee7"))) (file-name (git-file-name name version)) (sha256 (base32 "19iklfv1brwsfg1l5lrs3z8m343nskkn1998c1fs7fdn0lgrki2p")))) (build-system pyproject-build-system) (arguments (list #:phases #~(modify-phases %standard-phases ;; The md5 module has been removed in Python 3 (add-after 'unpack 'python3-compatibility (lambda _ (substitute* "tests/test_cli.py" (("import md5") "from hashlib import md5") (("md5.new") "md5") (("\\.digest") ".hexdigest"))))))) (propagated-inputs (list python-biopython python-click python-numpy python-optparse-pretty python-pandas python-pysam python-regex python-ruamel.yaml snakemake)) (native-inputs (list python-pytest)) (home-page "https://github.com/caleblareau/mgatk") (synopsis "Mitochondrial genome analysis toolkit.") (description "This package is a Python-based command line interface for processing .bam files with mitochondrial reads and generating high-quality heteroplasmy estimation from sequencing data. The mgatk package places a special emphasis on mitochondrial genotypes generated from single-cell genomics data, primarily @acronym{mtscATAC-seq, mitochondrial single-cell ATAC-sequence}, but is generally applicable across other assays.") (license license:expat))) (define-public python-multivelo (package (name "python-multivelo") (version "0.1.2") (source (origin (method url-fetch) (uri (pypi-uri "multivelo" version)) (sha256 (base32 "1b4qyngwagh5sc2ygyfqyirg63myzh1g1glk03a1ykxfii32cjlp")))) (build-system pyproject-build-system) (arguments (list #:tests? #f ;pypi source does not contain tests #:phases #~(modify-phases %standard-phases (add-before 'sanity-check 'set-env (lambda _ ;; numba RuntimeError: cannot cache function 'rdist' (setenv "NUMBA_CACHE_DIR" "/tmp")))))) (native-inputs (list python-pypa-build)) (propagated-inputs (list python-anndata python-h5py python-ipywidgets python-joblib python-loompy python-matplotlib python-numba python-numpy python-pandas python-scanpy python-scikit-learn python-scipy python-seaborn python-tqdm python-umap-learn scvelo)) (home-page "https://github.com/welch-lab/MultiVelo") (synopsis "Velocity inference from single-cell multi-omic data") (description "MultiVelo uses a probabilistic latent variable model to estimate the switch time and rate parameters of gene regulation, providing a quantitative summary of the temporal relationship between epigenomic and transcriptomic changes.") (license license:bsd-3))) (define-public python-mygene (package (name "python-mygene") (version "3.2.2") (source (origin (method url-fetch) (uri (pypi-uri "mygene" version)) (sha256 (base32 "1snszwdgfygchxshcbry3b5pbcw3g1isp8dw46razxccqaxwlag7")))) (build-system python-build-system) (propagated-inputs (list python-biothings-client)) (home-page "https://github.com/biothings/mygene.py") (synopsis "Python Client for MyGene.Info services") (description "MyGene.Info provides simple-to-use REST web services to query/retrieve gene annotation data. It's designed with simplicity and performance emphasized. Mygene is a Python wrapper to access MyGene.Info services.") (license license:bsd-3))) ;; We cannot use the latest commit because it requires Java 9. (define-public java-forester (let ((commit "86b07efe302d5094b42deed9260f719a4c4ac2e6") (revision "1")) (package (name "java-forester") (version (string-append "0-" revision "." (string-take commit 7))) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/cmzmasek/forester") (commit commit))) (file-name (string-append name "-" version "-checkout")) (sha256 (base32 "0vxavc1yrf84yrnf20dq26hi0lglidk8d382xrxsy4qmlbjd276z")) (modules '((guix build utils))) (snippet '(begin ;; Delete bundled jars and pre-built classes (delete-file-recursively "forester/java/resources") (delete-file-recursively "forester/java/classes") (for-each delete-file (find-files "forester/java/" "\\.jar$")) ;; Delete bundled applications (delete-file-recursively "forester_applications") #t)))) (build-system ant-build-system) (arguments `(#:tests? #f ; there are none #:jdk ,icedtea-8 #:modules ((guix build ant-build-system) (guix build utils) (guix build java-utils) (sxml simple) (sxml transform)) #:phases (modify-phases %standard-phases (add-after 'unpack 'chdir (lambda _ (chdir "forester/java") #t)) (add-after 'chdir 'fix-dependencies (lambda _ (chmod "build.xml" #o664) (call-with-output-file "build.xml.new" (lambda (port) (sxml->xml (pre-post-order (with-input-from-file "build.xml" (lambda _ (xml->sxml #:trim-whitespace? #t))) `(;; Remove all unjar tags to avoid repacking classes. (unjar . ,(lambda _ '())) (*default* . ,(lambda (tag . kids) `(,tag ,@kids))) (*text* . ,(lambda (_ txt) txt)))) port))) (rename-file "build.xml.new" "build.xml") #t)) ;; FIXME: itext is difficult to package as it depends on a few ;; unpackaged libraries. (add-after 'chdir 'remove-dependency-on-unpackaged-itext (lambda _ (delete-file "src/org/forester/archaeopteryx/PdfExporter.java") (substitute* "src/org/forester/archaeopteryx/MainFrame.java" (("pdf_written_to = PdfExporter.*") "throw new IOException(\"PDF export is not available.\");")) #t)) ;; There is no install target (replace 'install (install-jars "."))))) (propagated-inputs (list java-commons-codec java-openchart2)) (home-page "https://sites.google.com/site/cmzmasek/home/software/forester") (synopsis "Phylogenomics libraries for Java") (description "Forester is a collection of Java libraries for phylogenomics and evolutionary biology research. It includes support for reading, writing, and exporting phylogenetic trees.") (license license:lgpl2.1+)))) (define-public java-forester-1.005 (package (name "java-forester") (version "1.005") (source (origin (method url-fetch) (uri (string-append "https://repo1.maven.org/maven2/" "org/biojava/thirdparty/forester/" version "/forester-" version "-sources.jar")) (file-name (string-append name "-" version ".jar")) (sha256 (base32 "04r8qv4rk3p71z4ajrvp11py1z46qrx0047j3zzs79s6lnsm3lcv")))) (build-system ant-build-system) (arguments `(#:tests? #f ; there are none #:jdk ,icedtea-8 #:modules ((guix build ant-build-system) (guix build utils) (guix build java-utils) (sxml simple) (sxml transform)) #:phases (modify-phases %standard-phases (add-after 'unpack 'fix-dependencies (lambda* (#:key inputs #:allow-other-keys) (call-with-output-file "build.xml" (lambda (port) (sxml->xml (pre-post-order (with-input-from-file "src/build.xml" (lambda _ (xml->sxml #:trim-whitespace? #t))) `(;; Remove all unjar tags to avoid repacking classes. (unjar . ,(lambda _ '())) (*default* . ,(lambda (tag . kids) `(,tag ,@kids))) (*text* . ,(lambda (_ txt) txt)))) port))) (copy-file (assoc-ref inputs "synth_look_and_feel_1.xml") "synth_look_and_feel_1.xml") (copy-file (assoc-ref inputs "phyloxml.xsd") "phyloxml.xsd") (substitute* "build.xml" (("../resources/synth_laf/synth_look_and_feel_1.xml") "synth_look_and_feel_1.xml") (("../resources/phyloxml_schema/1.10/phyloxml.xsd") "phyloxml.xsd")) #t)) ;; FIXME: itext is difficult to package as it depends on a few ;; unpackaged libraries. (add-after 'unpack 'remove-dependency-on-unpackaged-itext (lambda _ (delete-file "src/org/forester/archaeopteryx/PdfExporter.java") (substitute* '("src/org/forester/archaeopteryx/MainFrame.java" "src/org/forester/archaeopteryx/MainFrameApplication.java") (("pdf_written_to = PdfExporter.*") "throw new IOException(\"PDF export is not available.\"); /*") ((".getPrintSizeX\$\$, getOptions\$\$.getPrintSizeY\$\$ \\);") "*/") (("getCurrentTreePanel\$\$.getHeight\$\$ \\);") "*/")) #t)) (add-after 'unpack 'delete-pre-built-classes (lambda _ (delete-file-recursively "src/classes") #t)) ;; There is no install target (replace 'install (install-jars "."))))) (propagated-inputs (list java-commons-codec java-openchart2)) ;; The source archive does not contain the resources. (native-inputs `(("phyloxml.xsd" ,(origin (method url-fetch) (uri (string-append "https://raw.githubusercontent.com/cmzmasek/forester/" "b61cc2dcede0bede317db362472333115756b8c6/" "forester/resources/phyloxml_schema/1.10/phyloxml.xsd")) (file-name (string-append name "-phyloxml-" version ".xsd")) (sha256 (base32 "1zxc4m8sn4n389nqdnpxa8d0k17qnr3pm2y5y6g6vh4k0zm52npv")))) ("synth_look_and_feel_1.xml" ,(origin (method url-fetch) (uri (string-append "https://raw.githubusercontent.com/cmzmasek/forester/" "29e04321615da6b35c1e15c60e52caf3f21d8e6a/" "forester/java/classes/resources/" "synth_look_and_feel_1.xml")) (file-name (string-append name "-synth-look-and-feel-" version ".xml")) (sha256 (base32 "1gv5602gv4k7y7713y75a4jvj7i9s7nildsbdl7n9q10sc2ikg8h")))))) (home-page "https://sites.google.com/site/cmzmasek/home/software/forester") (synopsis "Phylogenomics libraries for Java") (description "Forester is a collection of Java libraries for phylogenomics and evolutionary biology research. It includes support for reading, writing, and exporting phylogenetic trees.") (license license:lgpl2.1+))) (define-public java-biojava-core (package (name "java-biojava-core") (version "4.2.11") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/biojava/biojava") (commit (string-append "biojava-" version)))) (file-name (string-append name "-" version "-checkout")) (sha256 (base32 "1bvryh2bpsvash8ln79cmc9sqm8qw72hz4xzwqxcrjm8ssxszhqk")))) (build-system ant-build-system) (arguments `(#:jdk ,icedtea-8 #:jar-name "biojava-core.jar" #:source-dir "biojava-core/src/main/java/" #:test-dir "biojava-core/src/test" ;; These tests seem to require internet access. #:test-exclude (list "**/SearchIOTest.java" "**/BlastXMLParserTest.java" "**/GenbankCookbookTest.java" "**/GenbankProxySequenceReaderTest.java") #:phases (modify-phases %standard-phases (add-before 'build 'copy-resources (lambda _ (copy-recursively "biojava-core/src/main/resources" "build/classes") #t)) (add-before 'check 'copy-test-resources (lambda _ (copy-recursively "biojava-core/src/test/resources" "build/test-classes") #t))))) (propagated-inputs (list java-log4j-api java-log4j-core java-slf4j-api java-slf4j-simple)) (native-inputs (list java-junit java-hamcrest-core)) (home-page "https://biojava.org") (synopsis "Core libraries of Java framework for processing biological data") (description "BioJava is a project dedicated to providing a Java framework for processing biological data. It provides analytical and statistical routines, parsers for common file formats, reference implementations of popular algorithms, and allows the manipulation of sequences and 3D structures. The goal of the biojava project is to facilitate rapid application development for bioinformatics. This package provides the core libraries.") (license license:lgpl2.1+))) (define-public java-biojava-phylo (package (inherit java-biojava-core) (name "java-biojava-phylo") (build-system ant-build-system) (arguments `(#:jdk ,icedtea-8 #:jar-name "biojava-phylo.jar" #:source-dir "biojava-phylo/src/main/java/" #:test-dir "biojava-phylo/src/test" #:phases (modify-phases %standard-phases (add-before 'build 'copy-resources (lambda _ (copy-recursively "biojava-phylo/src/main/resources" "build/classes") #t)) (add-before 'check 'copy-test-resources (lambda _ (copy-recursively "biojava-phylo/src/test/resources" "build/test-classes") #t))))) (propagated-inputs (list java-log4j-api java-log4j-core java-slf4j-api java-slf4j-simple java-biojava-core java-forester)) (native-inputs (list java-junit java-hamcrest-core)) (home-page "https://biojava.org") (synopsis "Biojava interface to the forester phylogenomics library") (description "The phylo module provides a biojava interface layer to the forester phylogenomics library for constructing phylogenetic trees."))) (define-public java-biojava-alignment (package (inherit java-biojava-core) (name "java-biojava-alignment") (build-system ant-build-system) (arguments `(#:jdk ,icedtea-8 #:jar-name "biojava-alignment.jar" #:source-dir "biojava-alignment/src/main/java/" #:test-dir "biojava-alignment/src/test" #:phases (modify-phases %standard-phases (add-before 'build 'copy-resources (lambda _ (copy-recursively "biojava-alignment/src/main/resources" "build/classes") #t)) (add-before 'check 'copy-test-resources (lambda _ (copy-recursively "biojava-alignment/src/test/resources" "build/test-classes") #t))))) (propagated-inputs (list java-log4j-api java-log4j-core java-slf4j-api java-slf4j-simple java-biojava-core java-biojava-phylo java-forester)) (native-inputs (list java-junit java-hamcrest-core)) (home-page "https://biojava.org") (synopsis "Biojava API for genetic sequence alignment") (description "The alignment module of BioJava provides an API that contains @itemize @item implementations of dynamic programming algorithms for sequence alignment; @item reading and writing of popular alignment file formats; @item a single-, or multi- threaded multiple sequence alignment algorithm. @end itemize\n"))) (define-public java-biojava-core-4.0 (package (inherit java-biojava-core) (name "java-biojava-core") (version "4.0.0") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/biojava/biojava") (commit (string-append "biojava-" version)))) (file-name (string-append name "-" version "-checkout")) (sha256 (base32 "13675f6y9aqi7bi2lk3s1z7a22ynccjiqwa8izh7p97xi9wsfmd8")))))) (define-public java-biojava-phylo-4.0 (package (inherit java-biojava-core-4.0) (name "java-biojava-phylo") (build-system ant-build-system) (arguments `(#:jdk ,icedtea-8 #:jar-name "biojava-phylo.jar" #:source-dir "biojava-phylo/src/main/java/" #:test-dir "biojava-phylo/src/test" #:phases (modify-phases %standard-phases (add-before 'build 'copy-resources (lambda _ (copy-recursively "biojava-phylo/src/main/resources" "build/classes") #t)) (add-before 'check 'copy-test-resources (lambda _ (copy-recursively "biojava-phylo/src/test/resources" "build/test-classes") #t))))) (propagated-inputs (list java-log4j-api java-log4j-core java-slf4j-api java-slf4j-simple java-biojava-core-4.0 java-forester-1.005)) (native-inputs (list java-junit java-hamcrest-core)) (home-page "https://biojava.org") (synopsis "Biojava interface to the forester phylogenomics library") (description "The phylo module provides a biojava interface layer to the forester phylogenomics library for constructing phylogenetic trees."))) (define-public java-biojava-alignment-4.0 (package (inherit java-biojava-core-4.0) (name "java-biojava-alignment") (build-system ant-build-system) (arguments `(#:jdk ,icedtea-8 #:jar-name "biojava-alignment.jar" #:source-dir "biojava-alignment/src/main/java/" #:test-dir "biojava-alignment/src/test" #:phases (modify-phases %standard-phases (add-before 'build 'copy-resources (lambda _ (copy-recursively "biojava-alignment/src/main/resources" "build/classes") #t)) (add-before 'check 'copy-test-resources (lambda _ (copy-recursively "biojava-alignment/src/test/resources" "build/test-classes") #t))))) (propagated-inputs (list java-log4j-api java-log4j-core java-slf4j-api java-slf4j-simple java-biojava-core-4.0 java-biojava-phylo-4.0 java-forester-1.005)) (native-inputs (list java-junit java-hamcrest-core)) (home-page "https://biojava.org") (synopsis "Biojava API for genetic sequence alignment") (description "The alignment module of BioJava provides an API that contains @itemize @item implementations of dynamic programming algorithms for sequence alignment; @item reading and writing of popular alignment file formats; @item a single-, or multi- threaded multiple sequence alignment algorithm. @end itemize\n"))) (define-public dropseq-tools (package (name "dropseq-tools") (version "1.13") (source (origin (method url-fetch) (uri "http://mccarrolllab.com/download/1276/") (file-name (string-append "dropseq-tools-" version ".zip")) (sha256 (base32 "0yrffckxqk5l8b5xb6z4laq157zd9mdypr2p4b4vq2bhjzi1sj0s")) ;; Delete bundled libraries (modules '((guix build utils))) (snippet '(begin (for-each delete-file (find-files "jar/lib" "\\.jar$")) (delete-file-recursively "3rdParty"))))) (build-system ant-build-system) (arguments `(#:tests? #f ; test data are not included #:test-target "test" #:build-target "all" #:source-dir "public/src/" #:jdk ,icedtea-8 #:make-flags (list ,#~(string-append "-Dpicard.executable.dir=" #$(this-package-input "java-picard") "/share/java/")) #:modules ((ice-9 match) (srfi srfi-1) (guix build utils) (guix build java-utils) (guix build ant-build-system)) #:phases (modify-phases %standard-phases ;; FIXME: fails with "java.io.FileNotFoundException: ;; /gnu/store/…-dropseq-tools-1.13/share/java/lib/biojava-alignment.jar" (delete 'generate-jar-indices) ;; All dependencies must be linked to "lib", because that's where ;; they will be searched for when the Class-Path property of the ;; manifest is computed. (add-after 'unpack 'record-references (lambda* (#:key inputs #:allow-other-keys) (mkdir-p "jar/lib") (let ((dirs (filter-map (match-lambda ((name . dir) (if (and (string-prefix? "java-" name) (not (string=? name "java-testng"))) dir #f))) inputs))) (for-each (lambda (jar) (symlink jar (string-append "jar/lib/" (basename jar)))) (append-map (lambda (dir) (find-files dir "\\.jar$")) dirs))))) ;; There is no installation target (replace 'install (lambda* (#:key inputs outputs #:allow-other-keys) (let* ((out (assoc-ref outputs "out")) (bin (string-append out "/bin")) (share (string-append out "/share/java/")) (lib (string-append share "/lib/")) (scripts (list "BAMTagHistogram" "BAMTagofTagCounts" "BaseDistributionAtReadPosition" "CollapseBarcodesInPlace" "CollapseTagWithContext" "ConvertToRefFlat" "CreateIntervalsFiles" "DetectBeadSynthesisErrors" "DigitalExpression" "Drop-seq_alignment.sh" "FilterBAM" "FilterBAMByTag" "GatherGeneGCLength" "GatherMolecularBarcodeDistributionByGene" "GatherReadQualityMetrics" "PolyATrimmer" "ReduceGTF" "SelectCellsByNumTranscripts" "SingleCellRnaSeqMetricsCollector" "TagBamWithReadSequenceExtended" "TagReadWithGeneExon" "TagReadWithInterval" "TrimStartingSequence" "ValidateReference"))) (for-each mkdir-p (list bin share lib)) (install-file "dist/dropseq.jar" share) (for-each (lambda (script) (chmod script #o555) (install-file script bin)) scripts) (substitute* (map (lambda (script) (string-append bin "/" script)) scripts) (("^java") (which "java")) (("jar_deploy_dir=.*") (string-append "jar_deploy_dir=" share "\n")))))) ;; FIXME: We do this after stripping jars because we don't want it to ;; copy all these jars and strip them. We only want to install ;; links. Arguably, this is a problem with the ant-build-system. (add-after 'strip-jar-timestamps 'install-links (lambda* (#:key outputs #:allow-other-keys) (let* ((out (assoc-ref outputs "out")) (share (string-append out "/share/java/")) (lib (string-append share "/lib/"))) (for-each (lambda (jar) (symlink (readlink jar) (string-append lib (basename jar)))) (find-files "jar/lib" "\\.jar$")))))))) (inputs `(("jdk" ,icedtea-8) ("java-picard" ,java-picard-2.10.3) ("java-log4j-1.2-api" ,java-log4j-1.2-api) ("java-commons-math3" ,java-commons-math3) ("java-commons-jexl2" ,java-commons-jexl-2) ("java-commons-collections4" ,java-commons-collections4) ("java-commons-lang2" ,java-commons-lang) ("java-commons-io" ,java-commons-io) ("java-snappy-1.0.3-rc3" ,java-snappy-1) ("java-guava" ,java-guava) ("java-la4j" ,java-la4j) ("java-biojava-core" ,java-biojava-core-4.0) ("java-biojava-alignment" ,java-biojava-alignment-4.0) ("java-jdistlib" ,java-jdistlib) ("java-simple-xml" ,java-simple-xml) ("java-snakeyaml" ,java-snakeyaml))) (native-inputs (list unzip java-testng)) (home-page "http://mccarrolllab.com/dropseq/") (synopsis "Tools for Drop-seq analyses") (description "Drop-seq is a technology to enable biologists to analyze RNA expression genome-wide in thousands of individual cells at once. This package provides tools to perform Drop-seq analyses.") (license license:expat))) (define-public pigx-rnaseq (package (name "pigx-rnaseq") (version "0.1.1") (source (origin (method url-fetch) (uri (string-append "https://github.com/BIMSBbioinfo/pigx_rnaseq/" "releases/download/v" version "/pigx_rnaseq-" version ".tar.gz")) (sha256 (base32 "0mlas0srl04mvgsyydm67gg5syijf1k2f6dy7bdqqxc70fywfd08")))) (build-system gnu-build-system) (arguments `(#:parallel-tests? #f ; not supported #:phases (modify-phases %standard-phases ;; "test.sh" runs the whole pipeline, which takes a long time and ;; might fail due to OOM. The MultiQC is also resource intensive. (add-after 'unpack 'disable-resource-intensive-test (lambda _ (substitute* "Makefile.in" (("^ tests/test_multiqc/test.sh") "") (("^ test.sh") "")))) (add-before 'bootstrap 'autoreconf (lambda _ (invoke "autoreconf" "-vif"))) (add-before 'configure 'set-PYTHONPATH (lambda _ (setenv "PYTHONPATH" (getenv "GUIX_PYTHONPATH")))) (add-before 'check 'set-timezone ;; The readr package is picky about timezones. (lambda* (#:key inputs #:allow-other-keys) (setenv "TZ" "UTC+1") (setenv "TZDIR" (search-input-directory inputs "share/zoneinfo"))))))) (inputs (list coreutils sed gzip snakemake megadepth multiqc star-for-pigx hisat2 fastp htseq samtools r-minimal r-rmarkdown r-ggplot2 r-ggpubr r-ggrepel r-gprofiler2 r-deseq2 r-dt r-knitr r-pheatmap r-corrplot r-reshape2 r-plotly r-scales r-summarizedexperiment r-crosstalk r-tximport r-rtracklayer r-rjson salmon pandoc python-wrapper python-deeptools python-pyyaml)) (native-inputs (list tzdata automake autoconf)) (home-page "https://bioinformatics.mdc-berlin.de/pigx/") (synopsis "Analysis pipeline for RNA sequencing experiments") (description "PiGX RNAseq is an analysis pipeline for preprocessing and reporting for RNA sequencing experiments. It is easy to use and produces high quality reports. The inputs are reads files from the sequencing experiment, and a configuration file which describes the experiment. In addition to quality control of the experiment, the pipeline produces a differential expression report comparing samples in an easily configurable manner.") (license license:gpl3+))) (define-public pigx-chipseq (package (name "pigx-chipseq") (version "0.1.0") (source (origin (method url-fetch) (uri (string-append "https://github.com/BIMSBbioinfo/pigx_chipseq/" "releases/download/v" version "/pigx_chipseq-" version ".tar.gz")) (sha256 (base32 "008n6drj9q5av86xihxlj4py2c9p3c5z5ld89c3bksrp77zxiy67")))) (build-system gnu-build-system) (arguments `(#:tests? #f ; parts of the tests rely on access to the network #:phases (modify-phases %standard-phases (add-before 'configure 'set-PYTHONPATH (lambda _ (setenv "PYTHONPATH" (getenv "GUIX_PYTHONPATH"))))))) (inputs (list grep coreutils r-minimal r-argparser r-biocparallel r-biostrings r-chipseq r-corrplot r-data-table r-deseq2 r-dplyr r-dt r-genomation r-genomicalignments r-genomicranges r-ggplot2 r-ggrepel r-gprofiler2 r-heatmaply r-hexbin r-htmlwidgets r-jsonlite r-pheatmap r-plotly r-rmarkdown r-rsamtools r-rsubread r-rtracklayer r-s4vectors r-stringr r-tibble r-tidyr python-wrapper python-pyyaml python-magic python-xlrd trim-galore macs multiqc perl pandoc fastqc bowtie idr snakemake samtools bedtools kentutils)) (native-inputs (list python-pytest)) (home-page "https://bioinformatics.mdc-berlin.de/pigx/") (synopsis "Analysis pipeline for ChIP sequencing experiments") (description "PiGX ChIPseq is an analysis pipeline for preprocessing, peak calling and reporting for ChIP sequencing experiments. It is easy to use and produces high quality reports. The inputs are reads files from the sequencing experiment, and a configuration file which describes the experiment. In addition to quality control of the experiment, the pipeline enables to set up multiple peak calling analysis and allows the generation of a UCSC track hub in an easily configurable manner.") (license license:gpl3+))) (define-public pigx-bsseq (package (name "pigx-bsseq") (version "0.1.8") (source (origin (method url-fetch) (uri (string-append "https://github.com/BIMSBbioinfo/pigx_bsseq/" "releases/download/v" version "/pigx_bsseq-" version ".tar.gz")) (sha256 (base32 "1s8zgrqxabrawrgkga5rmgb0gyzj7ck47p3rkicjkfv7r2yjy0d7")))) (build-system gnu-build-system) (arguments `(;; TODO: tests currently require 12+GB of RAM. See ;; https://github.com/BIMSBbioinfo/pigx_bsseq/issues/164 #:tests? #f #:phases (modify-phases %standard-phases (add-before 'configure 'set-PYTHONPATH (lambda _ (setenv "PYTHONPATH" (getenv "GUIX_PYTHONPATH")))) (add-before 'check 'set-timezone ;; The readr package is picky about timezones. (lambda* (#:key inputs #:allow-other-keys) (setenv "TZ" "UTC+1") (setenv "TZDIR" (search-input-directory inputs "share/zoneinfo"))))))) (native-inputs (list tzdata)) (inputs (list coreutils sed grep r-minimal r-annotationhub r-dt r-genomation r-ggbio r-ggrepel r-matrixstats r-methylkit r-reshape2 r-rtracklayer r-rmarkdown r-bookdown r-ggplot2 r-ggbio pandoc python-wrapper python-pyyaml snakemake bismark bowtie bwa-meth fastqc methyldackel multiqc trim-galore cutadapt samblaster samtools)) (home-page "https://bioinformatics.mdc-berlin.de/pigx/") (synopsis "Bisulfite sequencing pipeline from fastq to methylation reports") (description "PiGx BSseq is a data processing pipeline for raw fastq read data of bisulfite experiments; it produces reports on aggregate methylation and coverage and can be used to produce information on differential methylation and segmentation.") (license license:gpl3+))) (define-public pigx-scrnaseq (package (name "pigx-scrnaseq") (version "1.1.9") (source (origin (method url-fetch) (uri (string-append "https://github.com/BIMSBbioinfo/pigx_scrnaseq/" "releases/download/v" version "/pigx_scrnaseq-" version ".tar.gz")) (sha256 (base32 "0adx7877c3lhlrzfid76i8bc829wcmzvrm0jx47gyid8mxqb7vqs")))) (build-system gnu-build-system) (arguments `(#:phases (modify-phases %standard-phases (add-before 'configure 'set-additional-environment-variables (lambda _ ;; Needed because of loompy (setenv "NUMBA_CACHE_DIR" "/tmp") ;; Needed to capture environment (setenv "PYTHONPATH" (getenv "GUIX_PYTHONPATH"))))))) (inputs (list coreutils perl fastqc flexbar icedtea-8 jellyfish python-wrapper python-pyyaml python-pandas python-magic python-numpy python-loompy pandoc samtools snakemake star-for-pigx r-minimal r-argparser r-cowplot r-data-table r-delayedarray r-delayedmatrixstats r-dplyr r-dropbead r-dt r-genomicalignments r-genomicfiles r-genomicranges r-ggplot2 r-hdf5array r-pheatmap r-rmarkdown r-rsamtools r-rtracklayer r-rtsne r-scater r-scran r-seurat r-singlecellexperiment r-stringr r-yaml)) (home-page "https://bioinformatics.mdc-berlin.de/pigx/") (synopsis "Analysis pipeline for single-cell RNA sequencing experiments") (description "PiGX scRNAseq is an analysis pipeline for preprocessing and quality control for single cell RNA sequencing experiments. The inputs are read files from the sequencing experiment, and a configuration file which describes the experiment. It produces processed files for downstream analysis and interactive quality reports. The pipeline is designed to work with UMI based methods.") (license license:gpl3+))) (define-public pigx-sars-cov-2 (package (name "pigx-sars-cov-2") (version "0.0.9") (source (origin (method url-fetch) (uri (string-append "https://github.com/BIMSBbioinfo/pigx_sars-cov-2" "/releases/download/v" version "/pigx_sars-cov-2-" version ".tar.gz")) (sha256 (base32 "168hrafgsn165q3hcdn916vlbl0zbzri1lckaqapbrcqk00izxma")))) (build-system gnu-build-system) (arguments (list #:phases '(modify-phases %standard-phases (add-after 'unpack 'unpack-databases (lambda* (#:key inputs #:allow-other-keys) ;; The tests need to be able to write caches to HOME. ;; They also default to reading the databases from there. (setenv "HOME" "/tmp") ;; Unpack the three databases in the expected location. (let ((root "/tmp/.local/share/pigx/databases") (use-underscore (lambda (c) (if (equal? c #\-) #\_ c)))) (for-each (lambda (db) (let ((where (string-append root "/" (string-map use-underscore db)))) (mkdir-p where) (invoke "tar" "-C" where "-xf" (assoc-ref inputs db)))) '("kraken-db" "krona-db" "vep-db"))))) (add-before 'configure 'set-PYTHONPATH (lambda _ (setenv "PYTHONPATH" (getenv "GUIX_PYTHONPATH"))))))) (native-inputs (let ((bimsb-origin (lambda (name hash) (origin (method url-fetch) (uri (string-append "https://bimsbstatic.mdc-berlin.de/akalin/AAkalin_pathogenomics" "/databases_small-20221006/" name)) (sha256 (base32 hash)))))) `(("kraken-db" ,(bimsb-origin "kraken_db.tar.gz" "0sdm4xh5npg6c3y2pz8xgphim4qpglm8wdid6rlaaqsn6iikv0mz")) ("krona-db" ,(bimsb-origin "krona_db.tar.gz" "1rwy4gd3vw1gdjldrgf44c1xaa3vq8i3pgisjhrac81yx63x8f2h")) ("vep-db" ,(bimsb-origin "vep_db.tar.gz" "0d8hhi43zsw3wqm7gd0z0gpcdsc6h6ra0imn87hifl9a64jxqzxz"))))) (inputs (list bash-minimal bedtools bwa ensembl-vep fastp fastqc ivar kraken2 krona-tools lofreq multiqc python-pyyaml python-wrapper r-base64url r-data-table r-deconvr r-dplyr r-dt r-ggplot2 r-htmltools r-jsonlite r-knitr r-magrittr r-mass r-minimal r-plotly r-qpcr r-r-utils r-reshape2 r-rmarkdown r-stringr r-tidyr r-viridis samtools snakemake wget)) (home-page "https://bioinformatics.mdc-berlin.de/pigx/") (synopsis "Analysis pipeline for wastewater sequencing") (description "PiGx SARS-CoV-2 is a pipeline for analysing data from sequenced wastewater samples and identifying given variants-of-concern of SARS-CoV-2. The pipeline can be used for continuous sampling. The output report will provide an intuitive visual overview about the development of variant abundance over time and location.") (license license:gpl3+))) (define-public pigx-sars-cov2-ww (deprecated-package "pigx-sars-cov2-ww" pigx-sars-cov-2)) (define-public pigx (package (name "pigx") (version "0.0.3") (source (origin (method url-fetch) (uri (string-append "https://github.com/BIMSBbioinfo/pigx/" "releases/download/v" version "/pigx-" version ".tar.gz")) (sha256 (base32 "1i5njdy1clj5ncw45d16p7mwmqvb1ilikl9n797pxklc3f4s7mq7")))) (build-system gnu-build-system) (inputs (list python pigx-bsseq pigx-chipseq pigx-rnaseq pigx-scrnaseq)) (home-page "https://bioinformatics.mdc-berlin.de/pigx/") (synopsis "Analysis pipelines for genomics") (description "PiGx is a collection of genomics pipelines. It includes the following pipelines: @itemize @item PiGx BSseq for raw fastq read data of bisulfite experiments @item PiGx RNAseq for RNAseq samples @item PiGx scRNAseq for single cell dropseq analysis @item PiGx ChIPseq for reads from ChIPseq experiments @end itemize All pipelines are easily configured with a simple sample sheet and a descriptive settings file. The result is a set of comprehensive, interactive HTML reports with interesting findings about your samples.") (license license:gpl3+))) (define-public genrich (package (name "genrich") (version "0.5") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/jsh58/Genrich") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "0x0q6z0208n3cxzqjla4rgjqpyqgwpmz27852lcvzkzaigymq4zp")))) (build-system gnu-build-system) (arguments `(#:tests? #f ; there are none #:phases (modify-phases %standard-phases (delete 'configure) (replace 'install (lambda* (#:key outputs #:allow-other-keys) (install-file "Genrich" (string-append (assoc-ref outputs "out") "/bin")) #t))))) (inputs (list zlib)) (home-page "https://github.com/jsh58/Genrich") (synopsis "Detecting sites of genomic enrichment") (description "Genrich is a peak-caller for genomic enrichment assays (e.g. ChIP-seq, ATAC-seq). It analyzes alignment files generated following the assay and produces a file detailing peaks of significant enrichment.") (license license:expat))) (define-public mantis ;; This is an arbitrary commit as a year has passed since 0.1 was tagged. (let ((commit "b6979a269172a45201c8366680d8b889f889432b") (revision "2")) (package (name "mantis") (version (git-version "0.1" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/splatlab/mantis") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0dq8a785hnaxx5kq757m5czs8xpcjpcph1inq2nm8h6zfvqyj8xs")))) (build-system cmake-build-system) (arguments '(#:tests? #f ; there are none #:configure-flags (list "-DNH=ON"))) ; do not use SSE4.2 instructions (inputs (list sdsl-lite openssl zlib)) (native-inputs (list gcc-7)) (home-page "https://github.com/splatlab/mantis") (synopsis "Large-scale sequence-search index data structure") (description "Mantis is a space-efficient data structure that can be used to index thousands of raw-read genomics experiments and facilitate large-scale sequence searches on those experiments. Mantis uses counting quotient filters instead of Bloom filters, enabling rapid index builds and queries, small indexes, and exact results, i.e., no false positives or negatives. Furthermore, Mantis is also a colored de Bruijn graph representation, so it supports fast graph traversal and other topological analyses in addition to large-scale sequence-level searches.") ;; uses __uint128_t and inline assembly (supported-systems '("x86_64-linux")) (license license:bsd-3)))) (define-public sjcount ;; There is no tag for version 3.2, nor is there a release archive. (let ((commit "292d3917cadb3f6834c81e509c30e61cd7ead6e5") (revision "1")) (package (name "sjcount") (version (git-version "3.2" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/pervouchine/sjcount-full") (commit commit))) (file-name (string-append name "-" version "-checkout")) (sha256 (base32 "0gdgj35j249f04rqgq8ymcc1xg1vi9kzbajnjqpaq2wpbh8bl234")))) (build-system gnu-build-system) (arguments `(#:tests? #f ; requires a 1.4G test file #:make-flags ,#~(list (string-append "SAMTOOLS_DIR=" #$(this-package-input "samtools") "/lib/")) #:phases (modify-phases %standard-phases (replace 'configure (lambda* (#:key inputs #:allow-other-keys) (substitute* "makefile" (("-I \\$\\{SAMTOOLS_DIR\\}") (string-append "-I" (assoc-ref inputs "samtools") "/include/samtools")) (("-lz ") "-lz -lpthread ")))) (replace 'install (lambda* (#:key outputs #:allow-other-keys) (for-each (lambda (tool) (install-file tool (string-append (assoc-ref outputs "out") "/bin"))) '("j_count" "b_count" "sjcount"))))))) (inputs (list samtools-0.1 zlib)) (home-page "https://github.com/pervouchine/sjcount-full/") (synopsis "Annotation-agnostic splice junction counting pipeline") (description "Sjcount is a utility for fast quantification of splice junctions in RNA-seq data. It is annotation-agnostic and offset-aware. This version does count multisplits.") (license license:gpl3+)))) (define-public minimap2 (package (name "minimap2") (version "2.28") (source (origin (method url-fetch) (uri (string-append "https://github.com/lh3/minimap2/" "releases/download/v" version "/" "minimap2-" version ".tar.bz2")) (sha256 (base32 "1d50j9fdmmaj7sdf4f49xddc235f7032lwh5ijgi2afj6lkp39gz")))) (build-system gnu-build-system) (arguments `(#:tests? #f ; there are none #:modules ((guix build utils) (guix build gnu-build-system) (srfi srfi-26)) #:make-flags (list (string-append "CC=" ,(cc-for-target)) (let ((system ,(or (%current-target-system) (%current-system)))) (cond ((or (string-prefix? "i586" system) (string-prefix? "i686" system)) "sse2only=1") ((string-prefix? "armhf" system) "arm_neon=1") ((string-prefix? "aarch64" system) "aarch64=1") (else "all")))) #:phases (modify-phases %standard-phases (delete 'configure) (replace 'install (lambda* (#:key outputs #:allow-other-keys) (let* ((out (assoc-ref outputs "out")) (bin (string-append out "/bin")) (lib (string-append out "/lib")) (inc (string-append out "/include")) (man (string-append out "/share/man/man1"))) (install-file "minimap2" bin) (install-file "libminimap2.a" lib) (install-file "minimap2.1" man) (map (cut install-file <> inc) (find-files "." "\\.h$")) ;; Not this file. (delete-file (string-append inc "/emmintrin.h")) (mkdir-p (string-append lib "/pkgconfig")) (with-output-to-file (string-append lib "/pkgconfig/minimap2.pc") (lambda _ (format #t "prefix=~a~@ exec_prefix=${prefix}~@ libdir=${exec_prefix}/lib~@ includedir=${prefix}/include~@ ~@ Name: libminimap2~@ Version: ~a~@ Description: A versatile pairwise aligner for genomic and spliced nucleotide sequence~@ Libs: -L${libdir} -lminimap2~@ Cflags: -I${includedir}~%" out ,version))))))))) (inputs (list zlib)) (home-page "https://lh3.github.io/minimap2/") (synopsis "Pairwise aligner for genomic and spliced nucleotide sequences") (description "Minimap2 is a versatile sequence alignment program that aligns DNA or mRNA sequences against a large reference database. Typical use cases include: @enumerate @item mapping PacBio or Oxford Nanopore genomic reads to the human genome; @item finding overlaps between long reads with error rate up to ~15%; @item splice-aware alignment of PacBio Iso-Seq or Nanopore cDNA or Direct RNA reads against a reference genome; @item aligning Illumina single- or paired-end reads; @item assembly-to-assembly alignment; @item full-genome alignment between two closely related species with divergence below ~15%. @end enumerate\n") (license license:expat))) (define-public python-mappy (package (name "python-mappy") (version "2.24") (source (origin (method url-fetch) (uri (pypi-uri "mappy" version)) (sha256 (base32 "1ycszza87p9qvx8mis9v1hry0ac465x1xcxbsn1k45qlxxrzp8im")))) (build-system python-build-system) (native-inputs (list python-cython)) (inputs (list zlib)) (home-page "https://github.com/lh3/minimap2") (synopsis "Python binding for minimap2") (description "This package provides a convenient interface to minimap2, a fast and accurate C program to align genomic and transcribe nucleotide sequences.") (license license:expat))) (define-public miniasm (package (name "miniasm") (version "0.3") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/lh3/miniasm") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "04dv5wv8bhsw1imxwyd438bnn9kby7svp44nbcz8lsadzjjci5gs")))) (build-system gnu-build-system) (inputs (list zlib)) (arguments `(#:tests? #f ; There are no tests. #:phases (modify-phases %standard-phases (delete 'configure) (replace 'install (lambda* (#:key inputs outputs #:allow-other-keys) (let ((bin (string-append (assoc-ref outputs "out") "/bin"))) (install-file "miniasm" bin) (install-file "minidot" bin) #t)))))) (home-page "https://github.com/lh3/miniasm") (synopsis "Ultrafast de novo assembly for long noisy reads") (description "Miniasm is a very fast OLC-based de novo assembler for noisy long reads. It takes all-vs-all read self-mappings (typically by minimap) as input and outputs an assembly graph in the GFA format. Different from mainstream assemblers, miniasm does not have a consensus step. It simply concatenates pieces of read sequences to generate the final unitig sequences. Thus the per-base error rate is similar to the raw input reads.") (license license:expat))) (define-public bandage (package (name "bandage") (version "0.8.1") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/rrwick/Bandage") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "1bbsn5f5x8wlspg4pbibqz6m5vin8c19nl224f3z3km0pkc97rwv")))) (build-system qt-build-system) (arguments (list ;; TODO: Once <https://issues.guix.gnu.org/47475> is fixed, ;; consider uncommenting the following: ;; ;; Prevent the (rarely updated) imagemagick/stable package from ;; ending up in the closure. ;; #:disallowed-references (list imagemagick/stable) #:phases #~(modify-phases %standard-phases (replace 'configure (lambda _ (invoke "qmake" "Bandage.pro"))) (replace 'check (lambda* (#:key tests? #:allow-other-keys) (when tests? (substitute* "tests/bandage_command_line_tests.sh" (("^bandagepath=.*") (string-append "bandagepath=" (getcwd) "/Bandage\n"))) (with-directory-excursion "tests" (setenv "XDG_RUNTIME_DIR" (getcwd)) (invoke "./bandage_command_line_tests.sh"))))) (replace 'install (lambda _ (install-file "Bandage" (string-append #$output "/bin"))))))) (inputs (list qtbase-5 qtsvg-5)) (native-inputs ;; imagemagick/stable cannot be used here, as it will end up in ;; the closure. See <https://issues.guix.gnu.org/47475>. (list imagemagick)) (home-page "https://rrwick.github.io/Bandage/") (synopsis "Bioinformatics Application for Navigating De novo Assembly Graphs Easily") (description "Bandage is a program for visualising de novo assembly graphs. It allows users to interact with the assembly graphs made by de novo assemblers such as Velvet, SPAdes, MEGAHIT and others. De novo assembly graphs contain not only assembled contigs but also the connections between those contigs, which were previously not easily accessible. Bandage visualises assembly graphs, with connections, using graph layout algorithms. Nodes in the drawn graph, which represent contigs, can be automatically labelled with their ID, length or depth. Users can interact with the graph by moving, labelling and colouring nodes. Sequence information can also be extracted directly from the graph viewer. By displaying connections between contigs, Bandage opens up new possibilities for analysing and improving de novo assemblies that are not possible by looking at contigs alone.") (license (list license:gpl2+ ; bundled ogdf license:gpl3+)))) (define-public libmaus2 (package (name "libmaus2") (version "2.0.786") (source (origin (method git-fetch) (uri (git-reference (url "https://gitlab.com/german.tischler/libmaus2") (commit (string-append version "-release-20210531143054")))) (file-name (git-file-name name version)) (sha256 (base32 "1rxakmwjcx2yq5sjh3v849f7dfw4xzc2fyzf6s28s3p95z84w564")))) (build-system gnu-build-system) ;; The test suite attempts to execute ../test-driver, which does not exist. (arguments '(#:tests? #false)) (propagated-inputs (list zlib)) (native-inputs (list pkg-config)) (home-page "https://gitlab.com/german.tischler/libmaus2") (synopsis "Collection of data structures and algorithms useful for bioinformatics") (description "libmaus2 is a collection of data structures and algorithms. It contains: @itemize @item I/O classes (single byte and UTF-8); @item @code{bitio} classes (input, output and various forms of bit level manipulation); @item text indexing classes (suffix and LCP array, fulltext and minute (FM), etc.); @item BAM sequence alignment files input/output (simple and collating); and many lower level support classes. @end itemize\n") ;; The code is explicitly available under the terms of either GPLv2 or ;; GPLv3 according to the AUTHORS file, though most files have a GPLv3+ ;; license header. (license (list license:gpl2+ license:gpl3+)))) (define-public biobambam2 (package (name "biobambam2") (version "2.0.182") (source (origin (method git-fetch) (uri (git-reference (url "https://gitlab.com/german.tischler/biobambam2") (commit (string-append version "-release-20210412001032")))) (file-name (git-file-name name version)) (sha256 (base32 "0b7w7a2a7hpkgrdn0n7hy4pilzrj82zqrh7q4bg1l0cd6bqr60m5")))) (build-system gnu-build-system) (arguments ;; The test suite attempts to execute ../test-driver, which does not exist. `(#:tests? #false #:configure-flags ,#~(list (string-append "--with-libmaus2=" #$(this-package-input "libmaus2"))))) (inputs (list libmaus2 xerces-c)) (native-inputs (list pkg-config)) (home-page "https://gitlab.com/german.tischler/biobambam2") (synopsis "Tools for processing BAM files") (description "This package contains some tools for processing BAM files including: @itemize @item bamsormadup: parallel sorting and duplicate marking @item bamcollate2: reads BAM and writes BAM reordered such that alignment or collated by query name @item bammarkduplicates: reads BAM and writes BAM with duplicate alignments marked using the BAM flags field @item bammaskflags: reads BAM and writes BAM while masking (removing) bits from the flags column @item bamrecompress: reads BAM and writes BAM with a defined compression setting. This tool is capable of multi-threading. @item bamsort: reads BAM and writes BAM resorted by coordinates or query name @item bamtofastq: reads BAM and writes FastQ; output can be collated or uncollated by query name. @end itemize ") ;; The COPYING file states that the code is distributed under version 3 of ;; the GPL, but the license headers include the "or later" clause. (license license:gpl3+))) (define-public r-disgenet2r (let ((commit "8d8ce37da7384004038b25e784b9f7cfe2353de1") (revision "1")) (package (name "r-disgenet2r") (version (git-version "0.99.2" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://bitbucket.org/ibi_group/disgenet2r") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0dvk75s6wqssdyfn5iczldb8krvrz2s0dslxns4571cb2pr09b84")))) (properties `((upstream-name . "disgenet2r"))) (build-system r-build-system) (propagated-inputs (list r-data-table r-ggplot2 r-gtable r-httr r-igraph r-jsonlite r-purrr r-reshape r-reshape2 r-sparql r-stringr r-tidyr r-tidyverse r-venndiagram)) (native-inputs (list r-knitr)) (home-page "https://bitbucket.org/ibi_group/disgenet2r") (synopsis "Query, visualize, and expand DisGeNET data") (description "This is an R package to query and expand DisGeNET data, and to visualize the results within R framework. The disgenet2r package is designed to retrieve data from DisGeNET v6.0 (Jan, 2019).") (license license:expat)))) (define-public r-dtmm (let ((commit "3a553b1e17d27d90a496d2e23e98e5dfe4abc266") (revision "1")) (package (name "r-dtmm") (version (git-version "0.1.0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/MaStatLab/DTMM") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "19279wafqfs9gk9489f8zsp52qcdb0mkxgvqszq4i733ckr2mmkk")))) (properties `((upstream-name . "DTMM"))) (build-system r-build-system) (propagated-inputs (list r-ape r-rcpp r-rcpparmadillo)) (home-page "https://github.com/MaStatLab/DTMM") (synopsis "Dirichlet-tree multinomial mixtures") (description "This package lets you perform unsupervised clustering of amplicon sequencing data in microbiome studies with the Dirichlet-tree Multinomial Mixtures.") (license license:cc0)))) ;; Needed for r-liana (define-public r-omnipathr/devel (let ((commit "679bb79e319af246a16968d27d64d8d6937a331a") (revision "1")) (package (name "r-omnipathr") (version (git-version "3.5.5" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/saezlab/omnipathr") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "10h6lyapyx4ik8r4kx5z2dly46jlf2v57caq4g6i0hzifyz2vgjq")))) (properties `((upstream-name . "OmnipathR"))) (build-system r-build-system) (arguments `(#:phases (modify-phases %standard-phases (add-after 'unpack 'set-HOME (lambda _ (setenv "HOME" "/tmp")))))) (propagated-inputs (list r-checkmate r-crayon r-curl r-digest r-dplyr r-httr r-igraph r-jsonlite r-later r-logger r-magrittr r-progress r-purrr r-rappdirs r-readr r-readxl r-rlang r-rvest r-stringr r-tibble r-tidyr r-tidyselect r-withr r-xml2 r-yaml)) (native-inputs (list r-knitr)) (home-page "https://github.com/saezlab/omnipathr") (synopsis "OmniPath web service client and more") (description "This package provides a client for the OmniPath web service and many other resources. It also includes functions to transform and pretty print some of the downloaded data, functions to access a number of other resources such as BioPlex, ConsensusPathDB, EVEX, Gene Ontology, Guide to Pharmacology (IUPHAR/BPS), Harmonizome, HTRIdb, Human Phenotype Ontology, InWeb InBioMap, KEGG Pathway, Pathway Commons, Ramilowski et al. 2015, RegNetwork, ReMap, TF census, TRRUST and Vinayagam et al. 2011. Furthermore, OmnipathR features a close integration with the NicheNet method for ligand activity prediction from transcriptomics data, and its R implementation @code{nichenetr}.") (license license:expat)))) (define-public r-liana (let ((commit "10d81773e0874de676eb106ce56e3cf9d4fe01d3") (revision "1")) (package (name "r-liana") (version (git-version "0.1.11" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/saezlab/liana/") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0b0m8i9kava36s3cn6vnn5vmiwvqwxmcq8jacy6ccshsji3kgp09")))) (properties `((upstream-name . "liana"))) (build-system r-build-system) (arguments (list #:phases '(modify-phases %standard-phases ;; This is needed to find ~/.config/OmnipathR/omnipathr.yml (add-after 'unpack 'set-HOME (lambda _ (setenv "HOME" "/tmp")))))) (propagated-inputs (list r-basilisk r-basilisk-utils r-complexheatmap r-dplyr r-ggplot2 r-magrittr r-omnipathr/devel r-purrr r-rcolorbrewer r-readr r-reticulate r-rlang r-scater r-scran r-scuttle r-seuratobject r-singlecellexperiment r-stringr r-tibble r-tidyr r-tidyselect)) (native-inputs (list r-knitr)) (home-page "https://github.com/saezlab/liana/") (synopsis "LIANA: a LIgand-receptor ANalysis frAmework") (description "LIANA provides a number of methods and resource for ligand-receptor interaction inference from scRNA-seq data.") (license license:gpl3)))) (define-public r-circus (package (name "r-circus") (version "0.1.7") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/BIMSBbioinfo/ciRcus") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "0d1jz7r81zbcy1gkppggkjmgjxyjhva69s3cdb01m3f0790m4fv0")))) (properties `((upstream-name . "ciRcus"))) (build-system r-build-system) (propagated-inputs (list r-annotationdbi r-annotationhub r-biocgenerics r-biomart r-data-table r-dbi r-genomeinfodb r-genomicfeatures r-genomicranges r-ggplot2 r-hash r-iranges r-rcolorbrewer r-rmysql r-rtracklayer r-s4vectors r-stringr r-summarizedexperiment)) (native-inputs (list r-knitr)) (home-page "https://github.com/BIMSBbioinfo/ciRcus") (synopsis "Annotation, analysis and visualization of circRNA data") (description "Circus is an R package for annotation, analysis and visualization of circRNA data. Users can annotate their circRNA candidates with host genes, gene featrues they are spliced from, and discriminate between known and yet unknown splice junctions. Circular-to-linear ratios of circRNAs can be calculated, and a number of descriptive plots easily generated.") (license license:artistic2.0))) (define-public r-domultibarheatmap (let ((commit "9e65afa0aa69fee631c61b7bf3e7742632c9cb95") (revision "1")) (package (name "r-domultibarheatmap") (version (git-version "0.1.0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/elliefewings/DoMultiBarHeatmap") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0q9mrc6md08aff6hhzlw3igvv3w7pr1wildzm8i0km9xvbi9iyy9")))) (properties `((upstream-name . "DoMultiBarHeatmap"))) (build-system r-build-system) (propagated-inputs (list r-ggplot2 r-magrittr r-rlang r-seurat)) (home-page "https://github.com/elliefewings/DoMultiBarHeatmap") (synopsis "Produce heatmap from a Seurat object with multiple annotation bars") (description "This package builds on Seurat's @code{Doheatmap} function code to produce a heatmap from a Seurat object with multiple annotation bars.") (license license:cc0)))) (define-public r-doubletfinder (let ((commit "554097ba4e2c0ed7c28dc7f0b5b75277f3a50551") (revision "1")) (package (name "r-doubletfinder") (version (git-version "2.0.3" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/chris-mcginnis-ucsf/DoubletFinder") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "1q1pnqw7ry4syp04wjmvz5bws6z4vg4c340ky07lk0vp577x2773")))) (properties `((upstream-name . "DoubletFinder"))) (build-system r-build-system) (propagated-inputs (list r-fields r-kernsmooth r-rocr)) (home-page "https://github.com/chris-mcginnis-ucsf/DoubletFinder") (synopsis "Identify doublets in single-cell RNA sequencing data") (description "DoubletFinder identifies doublets by generating artificial doublets from existing scRNA-seq data and defining which real cells preferentially co-localize with artificial doublets in gene expression space. Other DoubletFinder package functions are used for fitting DoubletFinder to different scRNA-seq datasets. For example, ideal DoubletFinder performance in real-world contexts requires optimal pK selection and homotypic doublet proportion estimation. pK selection is achieved using pN-pK parameter sweeps and maxima identification in mean-variance-normalized bimodality coefficient distributions. Homotypic doublet proportion estimation is achieved by finding the sum of squared cell annotation frequencies.") (license license:cc0)))) ;; There have been no releases. (define-public r-cytobackbone (let ((commit "4c1a0a35cc5ae1f8f516127cec92351d96fe26e7") (revision "1")) (package (name "r-cytobackbone") (version (git-version "1.0.0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/tchitchek-lab/CytoBackBone") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0ahiad14zcgdk42xzw5xryic2ibn2l8lkrcdvl2b5sz2js028yb3")))) (properties `((upstream-name . "CytoBackBone"))) (build-system r-build-system) (propagated-inputs (list r-flowcore r-flowutils r-fnn r-ggplot2 r-preprocesscore)) (native-inputs (list r-knitr)) (home-page "https://github.com/tchitchek-lab/CytoBackBone") (synopsis "Merge phenotype information from different cytometric profiles") (description "This package implements an algorithm which increases the number of simultaneously measurable markers and in this way helps with study of the immune responses. Thus, the present algorithm, named @code{CytoBackBone}, allows combining phenotypic information of cells from different cytometric profiles obtained from different cytometry panels. This computational approach is based on the principle that each cell has its own phenotypic and functional characteristics that can be used as an identification card. @code{CytoBackBone} uses a set of predefined markers, that we call the backbone, to define this identification card. The phenotypic information of cells with similar identification cards in the different cytometric profiles is then merged.") (license license:gpl2)))) (define-public r-cytoexplorer (let ((commit "0efb1cc19fc701ae03905cf1b8484c1dfeb387df") (revision "1")) (package (name "r-cytoexplorer") (version (git-version "1.1.0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/DillonHammill/CytoExploreR") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "1y7dadsy15i47rjmdq6ns80jzm6p0zmixll37q68ba2c7xn5pq3v")) (snippet '(delete-file "docs/articles/CytoExploreR_files/vis-4.20.1/vis.min.js")))) (properties `((upstream-name . "CytoExploreR"))) (build-system r-build-system) (arguments (list #:phases '(modify-phases %standard-phases (add-after 'unpack 'process-javascript (lambda* (#:key inputs #:allow-other-keys) (with-directory-excursion "docs/articles/CytoExploreR_files/" (let ((source (search-input-file inputs "/dist/vis.js")) (target "vis-4.20.1/vis.min.js")) (invoke "esbuild" source "--minify" (string-append "--outfile=" target))))))))) (propagated-inputs (list r-biocgenerics r-bslib r-data-table r-dplyr r-embedsom r-flowai r-flowcore r-flowworkspace r-gtools r-magrittr r-mass r-opencyto r-purrr r-rhandsontable r-robustbase r-rsvd r-rtsne r-shiny r-superheat r-tibble r-tidyr r-umap r-visnetwork)) (native-inputs `(("esbuild" ,esbuild) ("r-knitr" ,r-knitr) ("js-vis" ,(let ((version "4.20.1")) (origin (method git-fetch) (uri (git-reference (url "https://github.com/almende/vis") (commit (string-append "v" version)))) (file-name (git-file-name "js-vis" version)) (sha256 (base32 "09ldcqzzki5c0jlwas5992qjffqxnx6j5sl703qccfw7rg1hn469"))))))) (home-page "https://github.com/DillonHammill/CytoExploreR") (synopsis "Interactive analysis of cytometry data") (description "This package has been developed under ROpenSci gudelines to integrate conventional and cutting edge cytometry analysis tools under a unified framework. It aims to represent an intuitive and interactive approach to analysing cytometry data in R.") (license license:gpl2)))) (define-public r-giotto (let ((commit "3c8067cedbf6e3112edcac2ae796de05fd9d6fe4") (revision "1")) (package (name "r-giotto") (version (git-version "1.1.2" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/RubD/Giotto/") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "1nbbqs0jk07wafshvqsdp8ds3kr9bwq88aafc5m0kdiqs7winb0d")))) (properties `((upstream-name . "Giotto"))) (build-system r-build-system) (propagated-inputs (list r-clusterr r-complexheatmap r-cowplot r-data-table r-dbscan r-deldir r-farver r-fitdistrplus r-ggdendro r-ggplot2 r-ggraph r-ggrepel r-igraph r-irlba r-lfa r-limma r-magick r-magrittr r-matrix r-matrixstats r-plotly r-qvalue r-r-utils r-rcolorbrewer r-rcpp r-reshape2 r-reticulate r-rfast r-rlang r-rtsne r-scales r-uwot)) (native-inputs (list r-knitr)) (home-page "https://github.com/RubD/Giotto/") (synopsis "Spatial single-cell transcriptomics toolbox") (description "This package provides a toolbox to process, analyze and visualize spatial single-cell expression data.") (license license:expat)))) ;; Variant of r-illuminahumanmethylationepicmanifest in the ;; (gnu packages bioconductor) module. (define-public r-illuminahumanmethylationepicmanifest-latest (let ((commit "a9ffbad36f5e496ece6c4c37b80e2f4f7e02d0c3") (revision "1")) (package (name "r-illuminahumanmethylationepicmanifest") (version (git-version "1.0.0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/achilleasNP/IlluminaHumanMethylationEPICmanifest") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0v8f0hl0v8gwi61vgqw56rn5j09h95hj54rb8pzbn0znm162n4fc")))) (properties `((upstream-name . "IlluminaHumanMethylationEPICmanifest"))) (build-system r-build-system) (home-page "https://github.com/achilleasNP/IlluminaHumanMethylationEPICmanifest") (synopsis "Illumina Human Methylation Manifest 1.0 B5 for R and minfi") (description "This is a drop-in replacement for the @code{IlluminaHumanMethylationEPIC} package. It utilizes a Manifest based on 1.0B5 annotation. As of version 0.3.0, the @code{IlluminaHumanMethylationEPIC} package still employs the 1.0B2 annotation manifest. A corresponding annotation package, @code{IlluminaHumanMethylationEPICanno.ilm10b5.hg38}, is available to ensure proper annotation. The decision to maintain the same name is due to complications in downstream processing caused by array name lookup in certain preprocessing options.") (license license:artistic2.0)))) (define-public r-illuminahumanmethylationepicanno-ilm10b5-hg38 (let ((commit "3db06910e27f626e0cc8b335ff45cf9a4050a36a") (revision "1")) (package (name "r-illuminahumanmethylationepicanno-ilm10b5-hg38") (version (git-version "0.0.1" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/achilleasNP/IlluminaHumanMethylationEPICanno.ilm10b5.hg38") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0y8fhiwmkldi57f8nq64njfgljw68cm6pb1vh44hjwcc12k48sqr")))) (properties `((upstream-name . "IlluminaHumanMethylationEPICanno.ilm10b5.hg38"))) (build-system r-build-system) (propagated-inputs (list r-minfi)) (home-page "https://github.com/achilleasNP/IlluminaHumanMethylationEPICanno.ilm10b5.hg38") (synopsis "Illumina Human Methylation EPIC Annotation version 1.0B5") (description "This package provides a companion annotation file to the @code{IlluminaHumanMethylationEPICmanifest} package based on the same annotation 1.0B5.") (license license:artistic2.0)))) (define-public r-maxprobes (let ((commit "c2120dba972e12115280ef274ff80550cee5b264") (revision "1")) (package (name "r-maxprobes") (version (git-version "0.0.2" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/markgene/maxprobes") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "1kij9bds2l9mwm519bzyd2608563qjlmbrayhva1s0vgml5iq9wh")))) (properties `((upstream-name . "maxprobes"))) (build-system r-build-system) (propagated-inputs (list r-minfi r-minfidata)) (native-inputs (list r-knitr)) (home-page "https://github.com/markgene/maxprobes") (synopsis "Methylation array cross-reactive probes") (description "The Maxprobes package collects cross-reactive probes of Illumina methylation array 450K and EPIC/850K.") (license license:gpl2+)))) (define-public gffread ;; We cannot use the tagged release because it is not in sync with gclib. ;; See https://github.com/gpertea/gffread/issues/26 (let ((commit "ba7535fcb3cea55a6e5a491d916e93b454e87fd0") (revision "1")) (package (name "gffread") (version (git-version "0.9.12" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/gpertea/gffread") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "1dl2nbcg96lxpd0drg48ssa8343nf7pw9s9mkrc4mjjmfwsin3ki")))) (build-system gnu-build-system) (arguments `(#:tests? #f ; no check target #:make-flags (list "GCLDIR=gclib") #:phases (modify-phases %standard-phases (delete 'configure) (add-after 'unpack 'copy-gclib-source (lambda* (#:key inputs #:allow-other-keys) (mkdir-p "gclib") (copy-recursively (assoc-ref inputs "gclib-source") "gclib") #t)) ;; There is no install target (replace 'install (lambda* (#:key outputs #:allow-other-keys) (let* ((out (assoc-ref outputs "out")) (bin (string-append out "/bin"))) (install-file "gffread" bin)) #t))))) (native-inputs `(("gclib-source" ,(let ((version "0.10.3") (commit "54917d0849c1e83cfb057b5f712e5cb6a35d948f") (revision "1")) (origin (method git-fetch) (uri (git-reference (url "https://github.com/gpertea/gclib") (commit commit))) (file-name (git-file-name "gclib" version)) (sha256 (base32 "0b51lc0b8syrv7186fd7n8f15rwnf264qgfmm2palrwks1px24mr"))))))) (home-page "https://github.com/gpertea/gffread/") (synopsis "Parse and convert GFF/GTF files") (description "This package provides a GFF/GTF file parsing utility providing format conversions, region filtering, FASTA sequence extraction and more.") ;; gffread is under Expat, but gclib is under Artistic 2.0 (license (list license:expat license:artistic2.0))))) (define-public fit-sne (package (name "fit-sne") (version "1.2.1") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/KlugerLab/FIt-SNE") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "1imq4577awc226wvygf94kpz156qdfw8xl0w0f7ss4w10lhmpmf5")))) (build-system gnu-build-system) (arguments `(#:tests? #false ; there are none #:phases ;; There is no build system. (modify-phases %standard-phases (delete 'configure) (replace 'build (lambda _ (invoke "g++" "-std=c++11" "-O3" "src/sptree.cpp" "src/tsne.cpp" "src/nbodyfft.cpp" "-o" "bin/fast_tsne" "-pthread" "-lfftw3" "-lm" "-Wno-address-of-packed-member"))) (replace 'install (lambda* (#:key outputs #:allow-other-keys) (let* ((out (assoc-ref outputs "out")) (bin (string-append out "/bin")) (share (string-append out "/share/fit-sne"))) (for-each (lambda (file) (install-file file bin)) (find-files "bin")) (substitute* "fast_tsne.R" (("^FAST_TSNE_SCRIPT_DIR.*") (string-append "FAST_TSNE_SCRIPT_DIR = \"" out "\"\n"))) (install-file "fast_tsne.R" share))))))) (inputs (list fftw)) (home-page "https://github.com/KlugerLab/FIt-SNE") (synopsis "Fast Fourier Transform-accelerated interpolation-based t-SNE") (description "@dfn{t-Stochastic Neighborhood Embedding} (t-SNE) is a method for dimensionality reduction and visualization of high dimensional datasets. A popular implementation of t-SNE uses the Barnes-Hut algorithm to approximate the gradient at each iteration of gradient descent. This implementation differs in these ways: @itemize @item Instead of approximating the N-body simulation using Barnes-Hut, we interpolate onto an equispaced grid and use FFT to perform the convolution. @item Instead of computing nearest neighbors using vantage-point trees, we approximate nearest neighbors using the Annoy library. The neighbor lookups are multithreaded to take advantage of machines with multiple cores. @end itemize ") ;; See LICENSE.txt for details on what license applies to what files. (license (list license:bsd-4 license:expat license:asl2.0)))) (define-public python-scanpy (package (name "python-scanpy") (version "1.9.6") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/theislab/scanpy") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "12rz0a9151fkry6ws1a8p5wnc4n5qbjl6xlynj7kxy223iz8isds")))) (build-system pyproject-build-system) (arguments (list #:test-flags '(list "-k" ;; Plot tests that fail. (string-append "not test_clustermap" " and not test_dotplot_matrixplot_stacked_violin" " and not test_paga_compare" " and not test_paga_path" " and not test_paga_pie" " and not test_paga_plots" " and not test_violin" " and not test_scatter_no_basis_per_obs" ;; Type mismatch " and not test_obs_df" " and not test_var_df" ;; Minor accuracy problem " and not test_consistency[morans_i-allclose]" ;; These try to connect to the network " and not test_scrublet_plots" " and not test_plot_rank_genes_groups_gene_symbols" " and not test_pca_n_pcs" " and not test_pca_chunked" " and not test_pca_sparse" " and not test_pca_reproducible")) #:phases #~(modify-phases %standard-phases (add-after 'unpack 'pretend-version (lambda _ (setenv "SETUPTOOLS_SCM_PRETEND_VERSION" #$version))) (add-after 'unpack 'delete-bad-tests (lambda _ ;; These tests require Internet access. (delete-file-recursively "scanpy/tests/notebooks") (delete-file "scanpy/tests/test_clustering.py") (delete-file "scanpy/tests/test_datasets.py") (delete-file "scanpy/tests/test_normalization.py") (delete-file "scanpy/tests/test_score_genes.py") (delete-file "scanpy/tests/test_highly_variable_genes.py") ;; TODO: I can't get the plotting tests to work, even with Xvfb. (delete-file "scanpy/tests/test_embedding_plots.py") (delete-file "scanpy/tests/test_preprocessing.py") (delete-file "scanpy/tests/test_read_10x.py") ;; These two fail with "ValueError: I/O operation on closed file." (delete-file "scanpy/tests/test_neighbors_key_added.py") ;; The following tests requires 'scanorama', which isn't ;; packaged yet. (delete-file "scanpy/tests/external/test_scanorama_integrate.py") (setenv "PYTHONPATH" (string-append (getcwd) ":" #$(this-package-native-input "python-anndata:source") ":" (getenv "GUIX_PYTHONPATH"))))) ;; Numba needs a writable dir to cache functions. (add-before 'check 'set-numba-cache-dir (lambda _ (setenv "NUMBA_CACHE_DIR" "/tmp")))))) (propagated-inputs (list python-anndata python-dask python-h5py python-igraph python-joblib python-legacy-api-wrap python-louvain python-matplotlib python-natsort python-networkx python-numba python-packaging python-pandas python-patsy python-scikit-learn python-scipy python-seaborn python-session-info python-sinfo python-statsmodels python-tables python-pytoml python-tqdm python-umap-learn)) (native-inputs `(;; This package needs anndata.tests, which is not installed. ("python-anndata:source" ,(package-source python-anndata)) ("python-flit" ,python-flit) ("python-hatchling" ,python-hatchling) ("python-hatch-vcs" ,python-hatch-vcs) ("python-leidenalg" ,python-leidenalg) ("python-pytest" ,python-pytest) ("python-pytest-nunit" ,python-pytest-nunit) ("python-setuptools-scm" ,python-setuptools-scm))) (home-page "https://github.com/theislab/scanpy") (synopsis "Single-Cell Analysis in Python") (description "Scanpy is a scalable toolkit for analyzing single-cell gene expression data. It includes preprocessing, visualization, clustering, pseudotime and trajectory inference and differential expression testing. The Python-based implementation efficiently deals with datasets of more than one million cells.") (license license:bsd-3))) (define-public python-bbknn (package (name "python-bbknn") (version "1.6.0") (source (origin (method url-fetch) (uri (pypi-uri "bbknn" version)) (sha256 (base32 "06q43cpi7wi6f2d2jqs8f9rbd94pg1hh7978gm92mi9gvzbaj08w")))) (build-system pyproject-build-system) (arguments (list #:tests? #f ;no tests are included #:phases '(modify-phases %standard-phases ;; Numba needs a writable dir to cache functions. (add-before 'check 'set-numba-cache-dir (lambda _ (setenv "NUMBA_CACHE_DIR" "/tmp")))))) (propagated-inputs (list python-annoy python-cython python-numpy python-pandas python-pynndescent python-scikit-learn python-scipy python-umap-learn)) (native-inputs (list python-flit-core)) (home-page "https://github.com/Teichlab/bbknn") (synopsis "Batch balanced KNN") (description "BBKNN is a batch effect removal tool that can be directly used in the Scanpy workflow. It serves as an alternative to @code{scanpy.api.pp.neighbors()}, with both functions creating a neighbour graph for subsequent use in clustering, pseudotime and UMAP visualisation. If technical artifacts are present in the data, they will make it challenging to link corresponding cell types across different batches. BBKNN actively combats this effect by splitting your data into batches and finding a smaller number of neighbours for each cell within each of the groups. This helps create connections between analogous cells in different batches without altering the counts or PCA space.") (license license:expat))) (define-public python-drep (package (name "python-drep") (version "3.2.0") (source (origin (method url-fetch) (uri (pypi-uri "drep" version)) (sha256 (base32 "08vk0x6v5c5n7afgd5pcjhsvb424absypxy22hw1cm1n9kirbi77")))) (build-system python-build-system) (propagated-inputs (list python-biopython python-matplotlib python-numpy python-pandas python-pytest python-scikit-learn python-seaborn python-tqdm)) (home-page "https://github.com/MrOlm/drep") (synopsis "De-replication of microbial genomes assembled from multiple samples") (description "dRep is a Python program for rapidly comparing large numbers of genomes. dRep can also \"de-replicate\" a genome set by identifying groups of highly similar genomes and choosing the best representative genome for each genome set.") (license license:expat))) (define-public instrain (package (name "instrain") (version "1.5.4") (source (origin (method url-fetch) (uri (pypi-uri "inStrain" version)) (sha256 (base32 "05w1lw75x4lwkzg4qpi055g7hdjp9rnc4ksbxg2hfgksq9djk0hx")))) (build-system python-build-system) (arguments `(#:phases (modify-phases %standard-phases (add-after 'unpack 'patch-relative-imports (lambda _ (substitute* "docker/run_instrain.py" (("from s3_utils") "from .s3_utils") (("from job_utils") "from .job_utils"))))))) (inputs (list python-biopython-1.73 python-boto3 python-h5py python-lmfit python-matplotlib python-networkx python-numba python-numpy python-pandas python-psutil python-pysam python-scikit-learn python-seaborn python-tqdm ;; drep is needed for deprecated plot utilities python-drep)) (native-inputs (list python-pytest)) (home-page "https://github.com/MrOlm/inStrain") (synopsis "Calculation of strain-level metrics") (description "inStrain is a Python program for analysis of co-occurring genome populations from metagenomes that allows highly accurate genome comparisons, analysis of coverage, microdiversity, and linkage, and sensitive SNP detection with gene localization and synonymous non-synonymous identification.") ;; The tool itself says that the license is "MIT", but the repository ;; contains a LICENSE file with the GPLv3. ;; See https://github.com/MrOlm/inStrain/issues/51 (license license:expat))) (define-public gffcompare (let ((commit "be56ef4349ea3966c12c6397f85e49e047361c41") (revision "1")) (package (name "gffcompare") (version (git-version "0.10.15" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/gpertea/gffcompare/") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0cp5qpxdhw4mxpya5dld8wi3jk00zyklm6rcri426wydinrnfmkg")))) (build-system gnu-build-system) (arguments `(#:tests? #f ; no check target #:phases (modify-phases %standard-phases (delete 'configure) (add-before 'build 'copy-gclib-source (lambda* (#:key inputs #:allow-other-keys) (mkdir "../gclib") (copy-recursively (assoc-ref inputs "gclib-source") "../gclib") #t)) (replace 'install (lambda* (#:key outputs #:allow-other-keys) (let ((bin (string-append (assoc-ref outputs "out") "/bin"))) (install-file "gffcompare" bin) #t)))))) (native-inputs `(("gclib-source" ; see 'README.md' of gffcompare ,(let ((commit "54917d0849c1e83cfb057b5f712e5cb6a35d948f") (revision "1") (name "gclib") (version (git-version "0.10.3" revision commit))) (origin (method git-fetch) (uri (git-reference (url "https://github.com/gpertea/gclib/") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0b51lc0b8syrv7186fd7n8f15rwnf264qgfmm2palrwks1px24mr"))))))) (home-page "https://github.com/gpertea/gffcompare/") (synopsis "Tool for comparing or classifing transcripts of RNA-Seq") (description "@code{gffcompare} is a tool that can: @enumerate @item compare and evaluate the accuracy of RNA-Seq transcript assemblers (Cufflinks, Stringtie); @item collapse (merge) duplicate transcripts from multiple GTF/GFF3 files (e.g. resulted from assembly of different samples); @item classify transcripts from one or multiple GTF/GFF3 files as they relate to reference transcripts provided in a annotation file (also in GTF/GFF3 format). @end enumerate") (license (list license:expat ;license for gffcompare license:artistic2.0))))) ;license for gclib (define-public intervaltree (let ((commit "b90527f9e6d51cd36ecbb50429e4524d3a418ea5")) (package (name "intervaltree") (version (git-version "0.0.0" "1" commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/ekg/intervaltree/") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0rgv6q5fl4x5d74n6p5wvdna6zmbdbqpb4jqqh6vq3670gn08xad")))) (build-system gnu-build-system) (arguments `(#:tests? #f ; No tests. #:make-flags ,#~(list (string-append "PREFIX=" #$output) "DESTDIR=\"\"") #:phases (modify-phases %standard-phases (delete 'configure)))) ; There is no configure phase. (home-page "https://github.com/ekg/intervaltree") (synopsis "Minimal C++ interval tree implementation") (description "An interval tree can be used to efficiently find a set of numeric intervals overlapping or containing another interval. This library provides a basic implementation of an interval tree using C++ templates, allowing the insertion of arbitrary types into the tree.") (license license:expat)))) (define-public python-intervaltree (package (name "python-intervaltree") (version "3.1.0") (source (origin (method url-fetch) (uri (pypi-uri "intervaltree" version)) (sha256 (base32 "0bcm6c6r4ck9nfj9xwz4rm2swc5lrjvmw3lyl6rgj639jf41nawh")))) (build-system python-build-system) (arguments `(#:phases (modify-phases %standard-phases ;; pytest seems to have a check to make sure the user is testing ;; their checked-out code and not an installed, potentially ;; out-of-date copy. This is harmless here, since we just installed ;; the package, so we disable the check to avoid skipping tests ;; entirely. (add-before 'check 'import-mismatch-error-workaround (lambda _ (setenv "PY_IGNORE_IMPORTMISMATCH" "1") #t))))) (propagated-inputs (list python-sortedcontainers)) (native-inputs (list python-pytest)) (home-page "https://github.com/chaimleib/intervaltree") (synopsis "Editable interval tree data structure") (description "This package provides a mutable, self-balancing interval tree implementation for Python. Queries may be by point, by range overlap, or by range envelopment. This library was designed to allow tagging text and time intervals, where the intervals include the lower bound but not the upper bound.") (license license:asl2.0))) (define-public python-pypairix (package (name "python-pypairix") (version "0.3.7") ;; The tarball on pypi does not include the makefile to build the ;; programs. (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/4dn-dcic/pairix") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "1snr3lrmsld8sy77ng6ba6wcmd33xjccf1l2f3m6pi29xis9nd6p")))) (build-system python-build-system) (arguments `(#:phases (modify-phases %standard-phases (add-before 'build 'build-programs (lambda _ (invoke "make"))) (add-after 'install 'install-programs (lambda* (#:key outputs #:allow-other-keys) (copy-recursively "bin" (string-append (assoc-ref outputs "out") "/bin")) #t))))) (inputs (list zlib)) (home-page "https://github.com/4dn-dcic/pairix") (synopsis "Support for querying pairix-indexed bgzipped text files") (description "Pypairix is a Python module for fast querying on a pairix-indexed bgzipped text file that contains a pair of genomic coordinates per line.") (license license:expat))) (define-public python-pyrodigal (package (name "python-pyrodigal") (version "3.3.0") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/althonos/pyrodigal") (commit (string-append "v" version)) (recursive? #t))) (file-name (git-file-name name version)) (sha256 (base32 "10vxbm9i33wari0ifsr78xnfn7d0yqwzqpc5pchirjflf1mmnr6w")))) (build-system pyproject-build-system) (arguments (list #:modules '((ice-9 ftw) (srfi srfi-1) (srfi srfi-26) (guix build utils) (guix build pyproject-build-system)) #:phases #~(modify-phases %standard-phases (replace 'check (lambda* (#:key tests? #:allow-other-keys) (when tests? (let ((cwd (getcwd)) (libdir (find (cut string-prefix? "lib." <>) (scandir "build")))) (with-directory-excursion (string-append cwd "/build/" libdir) (invoke "python3" "-m" "unittest" "pyrodigal.tests" "-vv"))))))))) (propagated-inputs (list python-archspec python-importlib-resources)) (native-inputs (list python-cython-3 python-mock python-unittest2)) (home-page "https://github.com/althonos/pyrodigal") (synopsis "Cython bindings and Python interface for Prodigal") (description "This package offers Cython bindings and a Python interface for Prodigal. Prodigal is an ORF finder designed for both genomes and metagenomes.") (license license:gpl3))) (define-public python-pyfaidx (package (name "python-pyfaidx") (version "0.7.2.1") (source (origin (method url-fetch) (uri (pypi-uri "pyfaidx" version)) (sha256 (base32 "182ia2zg026lgphv68agxm9imw7649z9pdhfn8zkalrxkq5d5w1h")))) (build-system pyproject-build-system) (arguments (list #:test-flags ;; These tests require the download of large fasta.gz files. '(list "--ignore=tests/test_Fasta_bgzip.py") #:phases #~(modify-phases %standard-phases (add-after 'unpack 'fix-version (lambda _ (substitute* "pyproject.toml" (("dynamic = \\[\"version\"\\]") (string-append "version = \"" #$version "\"")))))))) (native-inputs (list python-fsspec python-mock python-numpy python-pytest python-pytest-cov)) (home-page "http://mattshirley.com") (synopsis "Random access to fasta subsequences") (description "This package provides procedures for efficient pythonic random access to fasta subsequences.") (license license:bsd-3))) (define-public python-cooler (package (name "python-cooler") (version "0.9.3") (source (origin (method url-fetch) (uri (pypi-uri "cooler" version)) (sha256 (base32 "0qqb0i5449r6w871klsbjzxsjhdkpsaas3hvs9f1hc7ssrkf1vi1")))) (build-system pyproject-build-system) (arguments (list #:test-flags '(list "-k" (string-append ;; These tests download files from the internet. "not test_fetch_chromsizes" " and not test_roundtrip" ;; This test depends on ipytree, which contains a lot of ;; minified JavaScript. " and not test_print_trees")))) (propagated-inputs (list python-asciitree python-biopython python-click python-cytoolz python-dask python-h5py python-multiprocess python-numpy python-pandas python-pyfaidx python-pypairix python-pysam python-pyyaml python-scipy python-simplejson)) (native-inputs (list python-coverage python-hatchling python-isort python-pytest python-pytest-cov)) ;; Almost all the projects of the Mirnylab are moved under Open2C umbrella (home-page "https://github.com/open2c/cooler") (synopsis "Sparse binary format for genomic interaction matrices") (description "Cooler is a support library for a sparse, compressed, binary persistent storage format, called @code{cool}, used to store genomic interaction data, such as Hi-C contact matrices.") (license license:bsd-3))) (define-public python-cooltools (package (name "python-cooltools") (version "0.7.0") (source (origin (method url-fetch) (uri (pypi-uri "cooltools" version)) (sha256 (base32 "076fgqzf6453cx5zs32vz0f5yvfg53w8ayq9s79jssy7gj2x89lb")))) (build-system pyproject-build-system) (native-inputs (list python-cython python-pytest)) (propagated-inputs (list python-bioframe python-click python-cooler python-joblib python-matplotlib python-multiprocess python-numba python-numpy python-pandas python-scikit-image python-scikit-learn python-scipy)) (home-page "https://github.com/open2c/cooltools") (synopsis "Analysis tools for genomic interaction data stored in .cool format") (description "This package provides necessary tools for the analysis of the genomic interaction data stored in @code{.cool} format. This collection of tools includes operations like compartment, insulation or peak calling.") (license license:expat))) (define-public python-hicmatrix (package (name "python-hicmatrix") (version "17.1") (source (origin ;;Pypi sources do not contain any test (method git-fetch) (uri (git-reference (url "https://github.com/deeptools/HiCMatrix") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "14gq7r9b64ff56l5f8h8zc2i2y3xri646jl0anb74japqxrwvlna")))) (build-system pyproject-build-system) (propagated-inputs (list python-cooler python-intervaltree python-numpy python-pandas python-scipy python-tables)) (native-inputs (list python-pytest)) (home-page "https://github.com/deeptools/HiCMatrix/") (synopsis "HiCMatrix class for HiCExplorer and pyGenomeTracks") (description "This helper package implements the @code{HiCMatrix} class for the HiCExplorer and pyGenomeTracks packages.") (license license:gpl3+))) (define-public python-hicexplorer (package (name "python-hicexplorer") (version "3.7.4") (source (origin ;; The latest version is not available on Pypi. (method git-fetch) (uri (git-reference (url "https://github.com/deeptools/HiCExplorer") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "1cjr9l0vcngd0f4dmar388ri1ah1bqybnn53jc85xwh07wfacq7l")))) (build-system pyproject-build-system) (arguments (list #:test-flags '(list "hicexplorer/test/general/" "--ignore" "hicexplorer/test/general/test_hicTADClassifier.py" "--ignore" "hicexplorer/test/general/test_hicTrainTADClassifier.py" "-k" (string-append ;; Unknown chromosome: ChrX "not test_build_matrix_restrictionCutFile_two" ;; fixture 'keepSelfLigation' not found " and not test_build_matrix_restrictionCutFile_six" ;; ValueError: object dtype is not supported by sparse matrices " and not test_hic_transfer_obs_exp_perChromosome" ;; No KR balancing available " and not test_correct_matrix_KR_partial_cool" " and not test_correct_matrix_KR_cool" " and not test_correct_matrix_KR_H5")) #:phases #~(modify-phases %standard-phases ;; See https://github.com/deeptools/Knight-Ruiz-Matrix-balancing-algorithm/issues/23 (add-after 'unpack 'remove-dependency-on-krbalancing (lambda _ (substitute* "hicexplorer/hicCorrectMatrix.py" (("from krbalancing import.*") "") (("( *)assert\$args.correctionMethod == 'KR'\$" m indent) (string-append m "\n" indent "log.error('krbalancing not available')\n" indent "exit(1)"))) (substitute* "setup.py" (("\"krbalancing >= 0.0.5\",") "")) (substitute* "requirements.txt" (("krbalancing >= 0.0.5") "")))) (add-after 'unpack 'fix-references (lambda _ (let ((site (string-append #$output "/lib/python" #$(version-major+minor (package-version python)) "/site-packages"))) (substitute* "hicexplorer/lib/tadClassifier.py" (("model_location = site.getsitepackages\$\$\\[0\\]") (string-append "model_location = \"" site "\"")))) (substitute* "hicexplorer/hicFindRestSite.py" (("subprocess.check_output\\(\\[\"cat\"") (string-append "subprocess.check_output([\"" (which "cat") "\"")) (("cmd = 'sort -k1") (string-append "cmd = '" (which "sort") " -k1"))))) ;; The tests aim to detect available memory and run more tests when ;; there is more available memory. Let's run them deterministically ;; instead and don't run any tests that require more than 1GB of ;; RAM. (add-after 'unpack 'run-only-low-mem-tests (lambda _ (with-directory-excursion "hicexplorer/test" (substitute* '("trivial_runs/test_hicBuildMatrix_trivial_runs_2.py" "trivial_runs/test_hicAggregateContacts_trivial_runs_five.py" "trivial_runs/test_hicAggregateContacts_trivial_runs_four.py" "trivial_runs/test_hicAggregateContacts_trivial_runs.py" "trivial_runs/test_hicAggregateContacts_trivial_runs_two_1.py" "trivial_runs/test_hicBuildMatrix_trivial_runs.py" "trivial_runs/test_hicAggregateContacts_trivial_runs_two_3.py" "trivial_runs/test_hicAggregateContacts_trivial_runs_three.py" "trivial_runs/test_hicAggregateContacts_trivial_runs_two.py" "trivial_runs/test_hicAggregateContacts_trivial_runs_two_2.py" "trivial_runs/test_hicAggregateContacts_trivial_runs_six.py" "general/test_hicDifferentialTAD.py" "general/test_hicDetectLoops.py" "general/test_hicPlotMatrix.py" "general/test_hicHyperoptDetectLoops.py" "general/test_hicCreateThresholdFile.py" "general/test_hicMergeDomains.py" "general/test_hicHyperoptDetectLoopsHiCCUPS.py" "general/test_hicAggregateContacts.py" "general/test_hicInterIntraTAD.py") (("^memory =.*") "memory = 1\n")))))))) (propagated-inputs (list python-biopython python-cleanlab python-cooler python-fit-nbinom python-future python-graphviz python-hic2cool python-hicmatrix python-hyperopt python-imbalanced-learn python-intervaltree python-ipykernel python-jinja2 python-matplotlib python-numpy python-pandas python-psutil python-pybedtools python-pybigwig python-pygenometracks python-pysam python-scikit-learn python-scipy python-tables python-tqdm python-unidecode)) (native-inputs (list graphviz)) ;for hicexplorer/test/test_compute_function.py (home-page "https://hicexplorer.readthedocs.io") (synopsis "Process, analyze and visualize Hi-C data") (description "HiCExplorer is a powerful and easy to use set of tools to process, normalize and visualize Hi-C data. HiCExplorer facilitates the creation of contact matrices, correction of contacts, TAD detection, A/B compartments, merging, reordering or chromosomes, conversion from different formats including cooler and detection of long-range contacts. Moreover, it allows the visualization of multiple contact matrices along with other types of data like genes, compartments, ChIP-seq coverage tracks (and in general any type of genomic scores), long range contacts and the visualization of viewpoints.") (license license:gpl3))) (define-public python-pygenometracks (package (name "python-pygenometracks") (version "3.5") (source (origin (method url-fetch) (uri (pypi-uri "pyGenomeTracks" version)) (sha256 (base32 "1l7smg2gc1vm2181lzmdnywb11gp6s6z6j444dbsigv65car8z8p")))) (build-system pyproject-build-system) (arguments (list #:tests? #f ;there are none #:phases '(modify-phases %standard-phases (add-after 'unpack 'relax-requirements (lambda _ (substitute* "setup.py" (("matplotlib ==3.1.1") "matplotlib >=3.1.1")))) (add-after 'unpack 'remove-invalid-syntax (lambda _ (substitute* "setup.py" ((".\\*,") ","))))))) (propagated-inputs (list python-future python-gffutils python-hicmatrix python-intervaltree python-matplotlib python-numpy python-pybigwig python-pysam python-tqdm)) (native-inputs (list python-pytest)) (home-page "https://pygenometracks.readthedocs.io") (synopsis "Program and library to plot beautiful genome browser tracks") (description "This package aims to produce high-quality genome browser tracks that are highly customizable. Currently, it is possible to plot: bigwig, bed (many options), bedgraph, links (represented as arcs), and Hi-C matrices. pyGenomeTracks can make plots with or without Hi-C data.") (license license:gpl3+))) (define-public python-iced (package (name "python-iced") (version "0.5.8") (source (origin (method url-fetch) (uri (pypi-uri "iced" version)) (sha256 (base32 "1avcjmpyyvhgbj5qca4l70ipiz7j3xmcw9p6rd9c06j99faa0r71")))) (build-system python-build-system) (arguments `(#:tests? #false)) ; there are none (propagated-inputs (list python-numpy python-pandas python-scipy python-scikit-learn)) (home-page "https://github.com/hiclib/iced") (synopsis "ICE normalization") (description "This is a package for normalizing Hi-C contact counts efficiently.") (license license:bsd-3))) (define-public python-hic2cool (package (name "python-hic2cool") (version "0.8.3") ;; pypi sources do not contain the test_data directory and no test can be ;; run (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/4dn-dcic/hic2cool") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "0dlnf0qfcp4jrc1nyya32a035c13xicyq16bwfnwhbb9s47mz7gl")))) (build-system python-build-system) (arguments `(#:phases (modify-phases %standard-phases ;; Two of the test-data files need to be writable. (add-after 'unpack 'make-test-data-writable (lambda _ (for-each make-file-writable (list "test_data/hic2cool_0.4.2_single_res.cool" "test_data/hic2cool_0.7.0_multi_res.mcool")))) ;; See https://github.com/4dn-dcic/hic2cool/issues/58 (add-after 'unpack 'fix-incompatibility-with-h5py-3 (lambda _ (substitute* "test.py" (("h5py.File\$fname\$") "h5py.File(fname, 'r')")) (substitute* "hic2cool/hic2cool_updates.py" (("h5py.File\$writefile\$") "h5py.File(writefile, 'a')")))) ;; These two tests fail for unknown reasons. (add-after 'unpack 'disable-broken-tests (lambda _ (substitute* "test.py" (("def test_convert") "def _test_convert"))))))) (propagated-inputs (list python-cooler python-h5py python-numpy python-pandas python-scipy)) (home-page "https://github.com/4dn-dcic/hic2cool") (synopsis "Converter for .hic and .cool files") (description "This package provides a converter between @code{.hic} files (from juicer) and single-resolution or multi-resolution @code{.cool} files (for cooler). Both @code{hic} and @code{cool} files describe Hi-C contact matrices.") (license license:expat))) (define-public python-scanorama (package (name "python-scanorama") (version "1.7.2") (source (origin (method url-fetch) (uri (pypi-uri "scanorama" version)) (sha256 (base32 "0il7bf4c7vli2dm2jx7dskh3ymgv8nmk0y90jzgfrnqjzh250x5w")))) (build-system python-build-system) (propagated-inputs (list python-annoy python-fbpca python-geosketch python-intervaltree python-matplotlib python-numpy python-scikit-learn python-scipy)) (home-page "https://github.com/brianhie/scanorama") (synopsis "Panoramic stitching of heterogeneous single cell transcriptomic data") (description "Scanorama enables batch-correction and integration of heterogeneous scRNA-seq datasets, which is described in the paper \"Efficient integration of heterogeneous single-cell transcriptomes using Scanorama\" by Brian Hie, Bryan Bryson, and Bonnie Berger.") (license license:expat))) (define-public r-pore (package (name "r-pore") (version "0.24") (source (origin (method url-fetch) (uri (string-append "mirror://sourceforge/rpore/" version "/poRe_" version ".tar.gz")) (sha256 (base32 "0pih9nljbv8g4x8rkk29i7aqq681b782r5s5ynp4nw9yzqnmmksv")))) (properties `((upstream-name . "poRe"))) (build-system r-build-system) (propagated-inputs (list r-bit64 r-data-table r-rhdf5 r-shiny r-svdialogs)) (home-page "https://sourceforge.net/projects/rpore/") (synopsis "Visualize Nanopore sequencing data") (description "This package provides graphical user interfaces to organize and visualize Nanopore sequencing data.") ;; This is free software but the license variant is unclear: ;; <https://github.com/mw55309/poRe_docs/issues/10>. (license license:bsd-3))) (define-public r-xbioc (let ((revision "1") (commit "6ff0670a37ab3036aaf1d94aa4b208310946b0b5")) (package (name "r-xbioc") (version (git-version "0.1.16" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/renozao/xbioc") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0w8bsq5myiwkfhh83nm6is5ichiyvwa1axx2szvxnzq39x6knf66")))) (build-system r-build-system) (propagated-inputs (list r-annotationdbi r-assertthat r-biobase r-biocmanager r-digest r-pkgmaker r-plyr r-reshape2 r-stringr)) (home-page "https://github.com/renozao/xbioc/") (synopsis "Extra base functions for Bioconductor") (description "This package provides extra utility functions to perform common tasks in the analysis of omics data, leveraging and enhancing features provided by Bioconductor packages.") (license license:gpl3+)))) (define-public r-cssam (let ((revision "1") (commit "9ec58c982fa551af0d80b1a266890d92954833f2")) (package (name "r-cssam") (version (git-version "1.4" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/shenorrLab/csSAM") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "128syf9v39gk0z3ip000qpsjbg6l1siyq6c8b0hz41dzg5achyb3")))) (build-system r-build-system) (propagated-inputs (list r-formula r-ggplot2 r-pkgmaker r-plyr r-rngtools r-scales)) (home-page "https://github.com/shenorrLab/csSAM/") (synopsis "Cell type-specific statistical analysis of microarray") (description "This package implements the method csSAM that computes cell-specific differential expression from measured cell proportions using SAM.") ;; Any version (license license:lgpl2.1+)))) (define-public r-bseqsc (let ((revision "1") (commit "fef3f3e38dcf3df37103348b5780937982b43b98")) (package (name "r-bseqsc") (version (git-version "1.0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/shenorrLab/bseqsc") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "1prw13wa20f7wlc3gkkls66n1kxz8d28qrb8icfqdwdnnv8w5qg8")))) (build-system r-build-system) (propagated-inputs (list r-abind r-annotationdbi r-biobase r-cssam r-dplyr r-e1071 r-edger r-ggplot2 r-nmf r-openxlsx r-pkgmaker r-plyr r-preprocesscore r-rngtools r-scales r-stringr r-xbioc)) (home-page "https://github.com/shenorrLab/bseqsc") (synopsis "Deconvolution of bulk sequencing experiments using single cell data") (description "BSeq-sc is a bioinformatics analysis pipeline that leverages single-cell sequencing data to estimate cell type proportion and cell type-specific gene expression differences from RNA-seq data from bulk tissue samples. This is a companion package to the publication \"A single-cell transcriptomic map of the human and mouse pancreas reveals inter- and intra-cell population structure.\" Baron et al. Cell Systems (2016) @url{https://www.ncbi.nlm.nih.gov/pubmed/27667365}.") (license license:gpl2+)))) (define-public porechop ;; The recommended way to install is to clone the git repository ;; https://github.com/rrwick/Porechop#installation (let ((commit "289d5dca4a5fc327f97b3f8cecb68ecaf1014861") (revision "1")) (package (name "porechop") (version (git-version "0.2.3" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/rrwick/Porechop") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "05ps43gig0d3ia9x5lj84lb00hbsl6ba9n7y7jz927npxbr2ym23")))) (build-system python-build-system) (home-page "https://github.com/rrwick/porechop") (synopsis "Finding, trimming or splitting adapters, in Oxford Nanopore reads") (description "The porechop package is a tool for finding and removing adapters from Oxford Nanopore reads. Adapters on the ends of reads are trimmed off, and when a read has an adapter in its middle, it is treated as chimeric and chopped into separate reads. Porechop performs thorough alignments to effectively find adapters, even at low sequence identity. Porechop also supports demultiplexing of Nanopore reads that were barcoded with the Native Barcoding Kit, PCR Barcoding Kit or Rapid Barcoding Kit.") (license license:gpl3+)))) (define-public jamm (package (name "jamm") (version "1.0.7.6") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/mahmoudibrahim/JAMM") (commit (string-append "JAMMv" version)))) (file-name (git-file-name name version)) (sha256 (base32 "0bsa5mf9n9q5jz7mmacrra41l7r8rac5vgsn6wv1fb52ya58b970")))) (build-system gnu-build-system) (arguments (list #:tests? #f ;there are none #:phases #~(modify-phases %standard-phases (delete 'configure) (delete 'build) (replace 'install (lambda _ (let ((libexec (string-append #$output "/libexec/jamm")) (bin (string-append #$output "/bin"))) (substitute* '("JAMM.sh" "SignalGenerator.sh") (("^sPath=.*") (string-append "sPath=\"" libexec "\"\n"))) (for-each (lambda (file) (install-file file libexec)) (list "bincalculator.r" "peakfinder.r" "peakhelper.r" "signalmaker.r" "xcorr.r" "xcorrhelper.r" ;; Perl scripts "peakfilter.pl" "readshifter.pl")) (for-each (lambda (script) (chmod script #o555) (install-file script bin) (wrap-program (string-append bin "/" script) `("PATH" ":" prefix (,(string-append #$(this-package-input "coreutils") "/bin") ,(string-append #$(this-package-input "gawk") "/bin") ,(string-append #$(this-package-input "perl") "/bin") ,(string-append #$(this-package-input "r-minimal") "/bin"))) `("PERL5LIB" ":" prefix (,(getenv "PERL5LIB"))) `("R_LIBS_SITE" ":" prefix (,(getenv "R_LIBS_SITE"))))) (list "JAMM.sh" "SignalGenerator.sh")))))))) (inputs (list bash coreutils gawk perl r-minimal ;;("r-parallel" ,r-parallel) r-signal r-mclust)) (home-page "https://github.com/mahmoudibrahim/JAMM") (synopsis "Peak finder for NGS datasets") (description "JAMM is a peak finder for next generation sequencing datasets (ChIP-Seq, ATAC-Seq, DNase-Seq, etc.) that can integrate replicates and assign peak boundaries accurately. JAMM is applicable to both broad and narrow datasets.") (license license:gpl3+))) (define-public ngless (package (name "ngless") (version "1.5.0") (source (origin (method url-fetch) (uri (hackage-uri "NGLess" version)) (sha256 (base32 "0pljyrlpr9r3cl5311dhgxdl8y40szyi4vprn34i3piy0qrldymi")))) (build-system haskell-build-system) (arguments `(#:haddock? #f #:phases (modify-phases %standard-phases (add-before 'configure 'update-constraints (lambda _ (substitute* "NGLess.cabal" (("\\b(base)\\s+[^,]+" all dep) dep)))) (add-after 'unpack 'create-Versions.hs (lambda _ (substitute* "NGLess/Dependencies/Versions.hs" (("bwaVersion = .+") (string-append "bwaVersion = \"" ,(package-version bwa) "\"")) (("samtoolsVersion = .+") (string-append "samtoolsVersion = \"" ,(package-version samtools) "\"")) (("prodigalVersion = .+") (string-append "prodigalVersion = \"" ,(package-version prodigal) "\"")) (("megahitVersion = .+") (string-append "megahitVersion = \"" ,(package-version megahit) "\"")) (("minimap2Version = .+") (string-append "minimap2Version = \"" ,(package-version minimap2) "\""))))) ;; See NGLess/FileManagement.hs. (add-after 'install 'wrap-program (lambda* (#:key inputs outputs #:allow-other-keys) (let* ((out (assoc-ref outputs "out")) (bwa (search-input-file inputs "/bin/bwa")) (samtools (search-input-file inputs "/bin/samtools")) (prodigal (search-input-file inputs "/bin/prodigal")) (minimap2 (search-input-file inputs "/bin/minimap2")) (megahit (search-input-file inputs "/bin/megahit"))) (wrap-program (string-append out "/bin/ngless") `("NGLESS_BWA_BIN" " " = (,bwa)) `("NGLESS_SAMTOOLS_BIN" " " = (,samtools)) `("NGLESS_PRODIGAL_BIN" " " = (,prodigal)) `("NGLESS_MINIMAP2_BIN" " " = (,minimap2)) `("NGLESS_MEGAHIT_BIN" " " = (,megahit)))))) ;; Sanity check. (add-after 'wrap-program 'check-install (lambda* (#:key outputs #:allow-other-keys) (let* ((ngless (string-append (assoc-ref outputs "out") "/bin/ngless"))) (invoke ngless "--check-install")))) (add-after 'register 'remove-libraries (lambda* (#:key outputs #:allow-other-keys) (delete-file-recursively (string-append (assoc-ref outputs "out") "/lib"))))))) (inputs (list bash-minimal prodigal bwa samtools minimap2 megahit ghc-missingh ghc-aeson ghc-ansi-terminal ghc-async ghc-atomic-write ghc-bytestring-lexing ghc-conduit ghc-conduit-algorithms ghc-conduit-extra ghc-configurator ghc-convertible ghc-data-default ghc-edit-distance ghc-either ghc-errors ghc-extra ghc-file-embed ghc-filemanip ghc-hashable ghc-hashtables ghc-hostname ghc-http-client ghc-http-conduit ghc-inline-c ghc-inline-c-cpp ghc-int-interval-map ghc-network ghc-optparse-applicative ghc-primitive ghc-random-shuffle ghc-regex ghc-resourcet ghc-safe ghc-stm-chans ghc-stm-conduit ghc-strict ghc-tar ghc-tar-conduit ghc-unix-compat ghc-unliftio ghc-unliftio-core ghc-vector ghc-vector-algorithms ghc-yaml ghc-zlib ghc-bzlib-conduit ghc-double-conversion ghc-safeio)) (propagated-inputs (list r-r6 r-hdf5r r-iterators r-itertools r-matrix)) (native-inputs (list ghc-hunit ghc-quickcheck ghc-tasty ghc-tasty-hunit ghc-tasty-quickcheck ghc-tasty-th)) (home-page "https://ngless.embl.de/") (synopsis "DSL for processing next-generation sequencing data") (description "Ngless is a domain-specific language for @dfn{next-generation sequencing} (NGS) data processing.") (license license:expat))) (define-public ghc-int-interval-map (let ((commit "678763de7fe6d7fa3f1c44b32d18ce58670270f4") (revision "1")) (package (name "ghc-int-interval-map") (version "0.0.0.0") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/ngless-toolkit/interval-to-int.git") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0fd728b5if89vj5j4f9y7k0b2xv2ycz5a21iy15wbdcf5bhim7i8")))) (build-system haskell-build-system) (inputs (list ghc-either ghc-primitive ghc-vector ghc-vector-algorithms)) (native-inputs (list ghc-hedgehog ghc-tasty ghc-tasty-hedgehog ghc-tasty-hunit ghc-tasty-quickcheck ghc-tasty-th)) (home-page "https://github.com/luispedro/interval-to-int#readme") (synopsis "Interval map structure in Haskell") (description "An interval map structure that is optimized for low memory (each interval is represented by about 3 words + whatever the cargo is) and has semantics that are appropriate for genomic intervals (namely, intervals can overlap and queries will return all matches together). It also designed to be used in two phases: a construction phase + query phase).") (license license:expat)))) (define-public filtlong ;; The recommended way to install is to clone the git repository ;; https://github.com/rrwick/Filtlong#installation ;; and the lastest release is more than nine months old (let ((commit "d1bb46dfe8bc7efe6257b5ce222c04bfe8aedaab") (revision "1")) (package (name "filtlong") (version (git-version "0.2.0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/rrwick/Filtlong") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "1xr92r820x8qlkcr3b57iw223yq8vjgyi42jr79w2xgw47qzr575")))) (build-system gnu-build-system) (arguments (list #:tests? #f ; no check target #:phases #~(modify-phases %standard-phases (delete 'configure) (replace 'install (lambda _ (let ((bin (string-append #$output "/bin")) (scripts (string-append #$output "/share/filtlong/scripts"))) (install-file "bin/filtlong" bin) (install-file "scripts/histogram.py" scripts) (install-file "scripts/read_info_histograms.sh" scripts)))) (add-after 'install 'wrap-program (lambda _ (let ((path (getenv "GUIX_PYTHONPATH"))) (wrap-program (string-append #$output "/share/filtlong/scripts/histogram.py") `("GUIX_PYTHONPATH" ":" prefix (,path)))))) (add-before 'check 'patch-tests (lambda _ (substitute* "scripts/read_info_histograms.sh" (("awk") (which "gawk")))))))) (inputs (list bash-minimal gawk ;for read_info_histograms.sh python-wrapper ;required for histogram.py zlib)) (home-page "https://github.com/rrwick/Filtlong/") (synopsis "Tool for quality filtering of Nanopore and PacBio data") (description "The Filtlong package is a tool for filtering long reads by quality. It can take a set of long reads and produce a smaller, better subset. It uses both read length (longer is better) and read identity (higher is better) when choosing which reads pass the filter.") (license (list license:gpl3 ;filtlong license:asl2.0))))) ;histogram.py (define-public nanopolish (package (name "nanopolish") (version "0.14.0") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/jts/nanopolish") (commit (string-append "v" version)) (recursive? #t))) (file-name (git-file-name name version)) (sha256 (base32 "1ha9v5ia0qrwgav0956cfc7n64wjm9a9w3rvkg21g37a994yixg5")) (modules '((guix build utils))) (snippet ;; TODO: unbundle slow5lib '(begin (for-each delete-file-recursively '("htslib" "minimap2")))))) (build-system gnu-build-system) (arguments (list #:make-flags #~(list "HDF5=noinstall" "EIGEN=noinstall" "HTS=noinstall" "MINIMAP2=noinstall" (string-append "CC=" #$(cc-for-target))) #:tests? #f ; no check target #:phases #~(modify-phases %standard-phases (add-after 'unpack 'find-eigen (lambda* (#:key inputs #:allow-other-keys) (setenv "CPATH" (string-append (search-input-directory inputs "/include/eigen3") ":" (or (getenv "CPATH") ""))))) (delete 'configure) (replace 'install (lambda _ (let ((bin (string-append #$output "/bin")) (scripts (string-append #$output "/share/nanopolish/scripts"))) (install-file "nanopolish" bin) (for-each (lambda (file) (install-file file scripts)) (find-files "scripts" ".*"))))) (add-after 'install 'wrap-programs (lambda* (#:key inputs #:allow-other-keys) (let ((pythonpath (getenv "GUIX_PYTHONPATH")) (perl5lib (getenv "PERL5LIB")) (scripts (string-append #$output "/share/nanopolish/scripts")) (guile (search-input-file inputs "bin/guile"))) (for-each (lambda (file) (wrap-program file `("GUIX_PYTHONPATH" ":" prefix (,pythonpath)))) (find-files scripts "\\.py")) (for-each (lambda (file) (wrap-script file #:guile guile `("PERL5LIB" ":" prefix (,perl5lib)))) (find-files scripts "\\.pl")))))))) (inputs (list bash-minimal guile-3.0 ;for wrappers eigen hdf5 htslib minimap2 perl bioperl-minimal perl-getopt-long python-wrapper python-biopython python-numpy python-pysam python-scikit-learn python-scipy zlib)) (native-inputs (list cmake-minimal)) (home-page "https://github.com/jts/nanopolish") (synopsis "Signal-level analysis of Oxford Nanopore sequencing data") (description "This package analyses the Oxford Nanopore sequencing data at signal-level. Nanopolish can calculate an improved consensus sequence for a draft genome assembly, detect base modifications, call SNPs (Single nucleotide polymorphisms) and indels with respect to a reference genome and more.") (license license:expat))) (define-public cnvkit (package (name "cnvkit") (version "0.9.10") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/etal/cnvkit") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "0r303pqjg70zpxa564bavbfj99c6di0dafgqqwx2vh4vfsiif94q")))) (build-system pyproject-build-system) (propagated-inputs (list python-biopython python-future python-matplotlib python-numpy python-pandas python-pomegranate python-pyfaidx python-pysam python-reportlab python-scikit-learn python-scipy ;; R packages r-dnacopy)) (inputs (list r-minimal)) ;for tests (home-page "https://cnvkit.readthedocs.org/") (synopsis "Copy number variant detection from targeted DNA sequencing") (description "CNVkit is a Python library and command-line software toolkit to infer and visualize copy number from high-throughput DNA sequencing data. It is designed for use with hybrid capture, including both whole-exome and custom target panels, and short-read sequencing platforms such as Illumina and Ion Torrent.") (license license:asl2.0))) (define-public python-pyfit-sne (package (name "python-pyfit-sne") (version "1.2.1") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/KlugerLab/pyFIt-SNE") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "0f3n7wcmxbnqiisgimhpa6p5chqpb1hj69i6rpg2hv2671i8nn68")))) (build-system python-build-system) (arguments '(#:tests? #false)) ; there are none (propagated-inputs (list python-numpy)) (inputs (list fftw)) (native-inputs (list python-cython)) (home-page "https://github.com/KlugerLab/pyFIt-SNE") (synopsis "FFT-accelerated Interpolation-based t-SNE") (description "t-Stochastic Neighborhood Embedding (t-SNE) is a highly successful method for dimensionality reduction and visualization of high dimensional datasets. A popular implementation of t-SNE uses the Barnes-Hut algorithm to approximate the gradient at each iteration of gradient descent. This package is a Cython wrapper for FIt-SNE.") (license license:bsd-4))) (define-public bbmap (package (name "bbmap") (version "39.01") (source (origin (method url-fetch) (uri (string-append "mirror://sourceforge/bbmap/BBMap_" version ".tar.gz")) (sha256 (base32 "1rlkw2mlkn699dk9n5lnigmvwq3zr2f8hnq9plx7zi1h06jqsq4q")))) (build-system ant-build-system) (arguments (list #:build-target "dist" #:tests? #f ; there are none #:make-flags #~(list (string-append "-Dmpijar=" #$(this-package-input "java-openmpi") "/lib/mpi.jar")) #:modules '((guix build ant-build-system) (guix build utils) (guix build java-utils)) #:phases #~(modify-phases %standard-phases (add-after 'build 'build-jni-library (lambda _ (with-directory-excursion "jni" (invoke "make" "-f" "makefile.linux")))) ;; There is no install target (replace 'install (install-jars "dist")) (add-after 'install 'install-scripts-and-documentation (lambda _ (substitute* "calcmem.sh" (("\\| awk ") (string-append "| " (which "awk") " "))) (let* ((scripts (find-files "." "\\.sh$")) (bin (string-append #$output "/bin")) (doc (string-append #$output "/share/doc/bbmap")) (jni (string-append #$output "/lib/jni"))) (substitute* scripts (("\\$DIR\"\"docs") doc) (("^CP=.*") (string-append "CP=" #$output "/share/java/BBTools.jar\n")) (("^NATIVELIBDIR.*") (string-append "NATIVELIBDIR=" jni "\n")) (("CMD=\"java") (string-append "CMD=\"" (which "java")))) (for-each (lambda (script) (install-file script bin)) scripts) ;; Install JNI library (install-file "jni/libbbtoolsjni.so" jni) ;; Install documentation (install-file "docs/readme.txt" doc) (copy-recursively "docs/guides" doc))))) #:jdk openjdk11)) (inputs (list gawk java-eclipse-jdt-core java-eclipse-jdt-compiler-apt java-openmpi)) (home-page "https://sourceforge.net/projects/bbmap/") (synopsis "Aligner and other tools for short sequencing reads") (description "This package provides bioinformatic tools to align, deduplicate, reformat, filter and normalize DNA and RNA-seq data. It includes the following tools: BBMap, a short read aligner for DNA and RNA-seq data; BBNorm, a kmer-based error-correction and normalization tool; Dedupe, a tool to simplify assemblies by removing duplicate or contained subsequences that share a target percent identity; Reformat, to convert reads between fasta/fastq/scarf/fasta+qual/sam, interleaved/paired, and ASCII-33/64, at over 500 MB/s; and BBDuk, a tool to filter, trim, or mask reads with kmer matches to an artifact/contaminant file.") (license license:bsd-3))) (define-public velvet (package (name "velvet") (version "1.2.10") (source (origin (method url-fetch) (uri (string-append "https://www.ebi.ac.uk/~zerbino/velvet/" "velvet_" version ".tgz")) (sha256 (base32 "0h3njwy66p6bx14r3ar1byb0ccaxmxka4c65rn4iybyiqa4d8kc8")) ;; Delete bundled libraries (modules '((guix build utils))) (snippet '(begin (delete-file "Manual.pdf") (delete-file-recursively "third-party"))))) (build-system gnu-build-system) (arguments (list #:make-flags #~(list "OPENMP=t") #:test-target "test" #:phases #~(modify-phases %standard-phases (delete 'configure) (add-after 'unpack 'fix-zlib-include (lambda _ (substitute* "src/binarySequences.c" (("../third-party/zlib-1.2.3/zlib.h") "zlib.h")))) (replace 'install (lambda _ (let ((bin (string-append #$output "/bin")) (doc (string-append #$output "/share/doc/velvet"))) (mkdir-p bin) (mkdir-p doc) (install-file "velveth" bin) (install-file "velvetg" bin) (install-file "Manual.pdf" doc) (install-file "Columbus_manual.pdf" doc))))))) (inputs (list openmpi zlib)) (native-inputs (list (texlive-updmap.cfg (list texlive-infwarerr texlive-kvoptions texlive-pdftexcmds)))) (home-page "https://www.ebi.ac.uk/~zerbino/velvet/") (synopsis "Nucleic acid sequence assembler for very short reads") (description "Velvet is a de novo genomic assembler specially designed for short read sequencing technologies, such as Solexa or 454. Velvet currently takes in short read sequences, removes errors then produces high quality unique contigs. It then uses paired read information, if available, to retrieve the repeated areas between contigs.") (license license:gpl2+))) (define-public vembrane (package (name "vembrane") (version "0.13.2") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/vembrane/vembrane") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "1gdih56gpqd8ks3sd4ah844kac09hi3g073k9gvazb32ah50900w")))) (build-system pyproject-build-system) (arguments (list #:phases '(modify-phases %standard-phases (add-after 'unpack 'relax-requirements (lambda _ (substitute* "pyproject.toml" (("pysam = \"\\^0.19\"") "pysam = \"^0.20\"") (("numpy = \\{ version = \"\\^1.23\"") "numpy = { version = \"^1\""))))))) (inputs (list python-asttokens python-intervaltree python-numpy python-pysam python-pyyaml)) (native-inputs (list poetry python-pytest)) (home-page "https://github.com/vembrane/vembrane") (synopsis "Filter VCF/BCF files with Python expressions.") (description "Vembrane allows to simultaneously filter variants based on any INFO or FORMAT field, CHROM, POS, ID, REF, ALT, QUAL, FILTER, and the annotation field ANN. When filtering based on ANN, annotation entries are filtered first. If no annotation entry remains, the entire variant is deleted.") (license license:expat))) (define-public python-velocyto (package (name "python-velocyto") (version "0.17.17") (source (origin (method url-fetch) (uri (pypi-uri "velocyto" version)) (sha256 (base32 "0fgygyzqgrq32dv6a00biq1p1cwi6kbl5iqblxq1kklj6b2mzmhs")) (modules '((guix build utils))) ;; Delete generated C files. (snippet '(for-each delete-file (find-files "." "\\.c"))))) (build-system python-build-system) (arguments '(#:phases (modify-phases %standard-phases ;; Numba needs a writable dir to cache functions. (add-before 'check 'set-numba-cache-dir (lambda _ (setenv "NUMBA_CACHE_DIR" "/tmp")))))) (native-inputs (list python-joblib)) (propagated-inputs (list python-click python-cython python-h5py python-loompy python-matplotlib python-numba python-numpy python-pandas python-pysam python-scikit-learn python-scipy)) (home-page "https://github.com/velocyto-team/velocyto.py") (synopsis "RNA velocity analysis for single cell RNA-seq data") (description "Velocyto is a library for the analysis of RNA velocity. Velocyto includes a command line tool and an analysis pipeline.") (license license:bsd-2))) (define-public arriba (package (name "arriba") (version "1.0.1") (source (origin (method url-fetch) (uri (string-append "https://github.com/suhrig/arriba/releases/" "download/v" version "/arriba_v" version ".tar.gz")) (sha256 (base32 "0jx9656ry766vb8z08m1c3im87b0c82qpnjby9wz4kcz8vn87dx2")))) (build-system gnu-build-system) (arguments (list #:tests? #f ;there are none #:phases #~(modify-phases %standard-phases (replace 'configure (lambda* (#:key inputs #:allow-other-keys) (substitute* "Makefile" (("-I\\$\$HTSLIB\$/htslib") (string-append "-I" (search-input-directory inputs "/include/htslib"))) ((" \\$\$HTSLIB\$/libhts.a") (string-append " " (search-input-file inputs "/lib/libhts.so")))) (let ((samtools (search-input-file inputs "/bin/samtools"))) (substitute* "run_arriba.sh" (("^STAR ") (string-append (search-input-file inputs "/bin/STAR") " ")) (("samtools --version-only") (string-append samtools " --version-only")) (("samtools index") (string-append samtools " index")) (("samtools sort") (string-append samtools " sort")))))) (replace 'install (lambda _ (let ((bin (string-append #$output "/bin"))) (install-file "arriba" bin) (install-file "run_arriba.sh" bin) (install-file "draw_fusions.R" bin) (wrap-program (string-append bin "/draw_fusions.R") `("R_LIBS_SITE" ":" prefix (,(getenv "R_LIBS_SITE")))))))))) (inputs (list bash-minimal htslib r-minimal r-circlize r-genomicalignments r-genomicranges samtools star zlib)) (home-page "https://github.com/suhrig/arriba") (synopsis "Gene fusion detection from RNA-Seq data") (description "Arriba is a command-line tool for the detection of gene fusions from RNA-Seq data. It was developed for the use in a clinical research setting. Therefore, short runtimes and high sensitivity were important design criteria. It is based on the fast STAR aligner and the post-alignment runtime is typically just around two minutes. In contrast to many other fusion detection tools which build on STAR, Arriba does not require to reduce the @code{alignIntronMax} parameter of STAR to detect small deletions.") ;; All code is under the Expat license with the exception of ;; "draw_fusions.R", which is under GPLv3. (license (list license:expat license:gpl3)))) (define-public adapterremoval (package (name "adapterremoval") (version "2.3.3") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/MikkelSchubert/adapterremoval") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "0wyr182667wqdmzhwwa6f7dddr8kk0scgzb8lsm23wim544mvn6i")))) (build-system gnu-build-system) (arguments (list #:make-flags #~(list "COLOR_BUILD=no" (string-append "PREFIX=" #$output)) #:test-target "test" #:phases '(modify-phases %standard-phases (delete 'configure)))) (inputs (list zlib)) (home-page "https://adapterremoval.readthedocs.io/") (synopsis "Rapid sequence adapter trimming, identification, and read merging") (description "This program searches for and removes remnant adapter sequences from @dfn{High-Throughput Sequencing} (HTS) data and (optionally) trims low quality bases from the 3' end of reads following adapter removal. AdapterRemoval can analyze both single end and paired end data, and can be used to merge overlapping paired-ended reads into (longer) consensus sequences. Additionally, the AdapterRemoval may be used to recover a consensus adapter sequence for paired-ended data, for which this information is not available.") (license license:gpl3+))) (define-public checkm (package (name "checkm") (version "1.1.3") (source (origin (method url-fetch) (uri (pypi-uri "checkm-genome" version)) (sha256 (base32 "0i2nnki639hgjag17wlva2x0ymn37b4krqsf6akxddykhfbkdnkz")))) (build-system python-build-system) (arguments `(#:tests? #f ; Some tests fail for unknown reasons. #:phases (modify-phases %standard-phases (add-before 'check 'set-HOME (lambda _ (setenv "HOME" "/tmp")))))) (inputs (list python-dendropy python-matplotlib python-numpy python-pysam python-scipy)) (home-page "https://ecogenomics.github.io/CheckM/") (synopsis "Assess the quality of putative genome bins") (description "CheckM provides a set of tools for assessing the quality of genomes recovered from isolates, single cells, or metagenomes. It provides robust estimates of genome completeness and contamination by using collocated sets of genes that are ubiquitous and single-copy within a phylogenetic lineage. Assessment of genome quality can also be examined using plots depicting key genomic characteristics (e.g., GC, coding density) which highlight sequences outside the expected distributions of a typical genome. CheckM also provides tools for identifying genome bins that are likely candidates for merging based on marker set compatibility, similarity in genomic characteristics, and proximity within a reference genome.") (license license:gpl3+))) (define-public umi-tools (package (name "umi-tools") (version "1.0.0") (source (origin (method url-fetch) (uri (pypi-uri "umi_tools" version)) (sha256 (base32 "08y3vz1vcx09whmbsn722lcs6jl9wyrh9i4p3k8j4cb1i32bij4a")))) (build-system python-build-system) (inputs (list python-pandas python-future python-scipy python-matplotlib python-regex python-pysam)) (native-inputs (list python-cython)) (home-page "https://github.com/CGATOxford/UMI-tools") (synopsis "Tools for analyzing unique modular identifiers") (description "This package provides tools for dealing with @dfn{Unique Molecular Identifiers} (UMIs) and @dfn{Random Molecular Tags} (RMTs) in genetic sequences. There are six tools: the @code{extract} and @code{whitelist} commands are used to prepare a fastq containing UMIs @code{+/-} cell barcodes for alignment. The remaining commands, @code{group}, @code{dedup}, and @{count}/@code{count_tab}, are used to identify PCR duplicates using the UMIs and perform different levels of analysis depending on the needs of the user.") (license license:expat))) (define-public ataqv (package (name "ataqv") (version "1.0.0") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/ParkerLab/ataqv") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "031xr6jx1aprh26y5b1lv3gzrlmzg4alfl73vvshymx8cq8asrqi")))) (build-system gnu-build-system) (arguments `(#:make-flags ,#~(list (string-append "prefix=" #$output) (string-append "BOOST_ROOT=" #$(this-package-input "boost")) (string-append "HTSLIB_ROOT=" #$(this-package-input "htslib"))) #:test-target "test" #:phases (modify-phases %standard-phases (delete 'configure)))) (inputs (list boost htslib ncurses zlib)) (native-inputs (list lcov)) (home-page "https://github.com/ParkerLab/ataqv") (synopsis "Toolkit for quality control and visualization of ATAC-seq data") (description "This package provides a toolkit for measuring and comparing ATAC-seq results. It was written to make it easier to spot differences that might be caused by ATAC-seq library prep or sequencing. The main program, @code{ataqv}, examines aligned reads and reports some basic metrics.") (license license:gpl3+))) (define-public r-psiplot (package (name "r-psiplot") (version "2.3.0") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/kcha/psiplot") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "08438h16cfry5kqh3y9hs8q1b1a8bxhblsm75knviz5r6q0n1jxh")))) (build-system r-build-system) (propagated-inputs (list r-mass r-dplyr r-tidyr r-purrr r-readr r-magrittr r-ggplot2)) (home-page "https://github.com/kcha/psiplot") (synopsis "Plot percent spliced-in values of alternatively-spliced exons") (description "PSIplot is an R package for generating plots of @dfn{percent spliced-in} (PSI) values of alternatively-spliced exons that were computed by vast-tools, an RNA-Seq pipeline for alternative splicing analysis. The plots are generated using @code{ggplot2}.") (license license:expat))) (define-public r-scopeloomr (let ((commit "99726f5f7da794042036b73924b6a10d6e7b4d5d") (revision "1")) (package (name "r-scopeloomr") (version (git-version "0.13.0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/aertslab/SCopeLoomR") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "1ci17ms0c0hf7yfp9ckcg7a2y1s0nm19jj3cifsd55hwc0gdglmz")))) (properties `((upstream-name . "SCopeLoomR"))) (build-system r-build-system) (propagated-inputs (list r-base64enc r-hdf5r r-igraph r-matrix r-plyr r-rjson r-rlist)) (home-page "https://github.com/aertslab/SCopeLoomR") (synopsis "Build .loom files and extract data from them") (description "This is an R package to build generic @code{.loom} files aligning with the default naming convention of the @code{.loom} format and to integrate other data types e.g.: regulons (SCENIC), clusters from Seurat, trajectory information... The package can also be used to extract data from @code{.loom} files.") (license license:expat)))) (define-public rscape (package (name "rscape") (version "2.0.0.q") (source (origin (method url-fetch) (uri (string-append "http://eddylab.org/software/rscape/" "rscape_v" version ".tar.gz")) (sha256 (base32 "1jabvm3fzh8iy4803ns12v1fsy28x6wdy8wx4ik8y0mfac4h787q")))) (build-system gnu-build-system) (propagated-inputs (list gsl openmpi)) (native-inputs (list automake autoconf)) (home-page "https://github.com/EddyRivasLab/R-scape") (synopsis "RNA structural covariation above phylogenetic expectation") (description "R-scape discovers RNA secondary structure consensus elements. These elements include riboswitches and ribozymes. It utilizes probabilistic modeling of sequence alignments, explicitly considering folding dependencies. The tool enables the de novo search for new structural elements and facilitates comparative analysis of known RNA families.") (license license:bsd-3))) (define-public r-databaselinke-r (let ((commit "cf3d6cc3d36f2e1c9a557390232e9a8ed5abb7fd") (revision "1")) (package (name "r-databaselinke-r") (version (git-version "1.7.0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/vertesy/DatabaseLinke.R") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0hk76sb3w1v8a7c1knpc572ypsbgqlrv0p49c9y55a0dr12n16s1")))) (properties `((upstream-name . "DatabaseLinke.R"))) (build-system r-build-system) (propagated-inputs (list r-readwriter)) (home-page "https://github.com/vertesy/DatabaseLinke.R") (synopsis "Parse links to databases from your list of gene symbols") (description "This package provides a set of functions to parse and open (search query) links to genomics related and other websites for R. Useful when you want to explore e.g.: the function of a set of differentially expressed genes.") (license license:gpl3)))) (define-public r-seurat-utils (let ((commit "c0374cc9e25ce391ba8013fda0f8c7babbb9201d") (revision "1")) (package (name "r-seurat-utils") (version (git-version "2.5.0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/vertesy/Seurat.utils") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "15l86b43q245gzz7gsr5rhs4sir74lc14d64yqxfqcb0zrb2bzzd")))) (properties `((upstream-name . "Seurat.utils"))) (build-system r-build-system) (propagated-inputs (list r-codeandroll2 r-cowplot r-databaselinke-r r-dplyr r-enhancedvolcano r-foreach r-ggcorrplot r-ggexpress r-ggplot2 r-ggpubr r-ggrepel r-hgnchelper r-htmlwidgets r-job r-magrittr r-markdownhelpers r-markdownreports r-matrix r-matrixstats r-pheatmap r-plotly r-princurve r-qs r-r-utils r-readr r-readwriter r-reshape2 r-rstudioapi r-scales r-seurat r-soupx r-sparsematrixstats r-stringendo r-stringr r-tibble r-tictoc r-tidyverse r-vroom)) (home-page "https://github.com/vertesy/Seurat.utils") (synopsis "Collection of utility functions for Seurat") (description "This is a collection of utility functions for Seurat. These functions allow the automation and multiplexing of plotting, 3D plotting, visualization of statistics & QC, interaction with the Seurat object. Some functionalities require functions from CodeAndRoll and MarkdownReports libraries.") (license license:gpl3)))) (define-public r-seuratwrappers ;; There are no releases or tags. (let ((commit "d28512f804d5fe05e6d68900ca9221020d52cf1d") (revision "1")) (package (name "r-seuratwrappers") (version (git-version "0.3.1" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/satijalab/seurat-wrappers") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0rm74y2fj3cmiqn7jz1ald8jbw53c2qxkj3mgl4pxih9vx39jhgy")))) (properties `((upstream-name . "SeuratWrappers"))) (build-system r-build-system) (propagated-inputs (list r-biocmanager r-cowplot r-ggplot2 r-igraph r-matrix r-remotes r-rlang r-rsvd r-r-utils r-seurat)) (home-page "https://github.com/satijalab/seurat-wrappers") (synopsis "Community-provided methods and extensions for the Seurat object") (description "SeuratWrappers is a collection of community-provided methods and extensions for Seurat, curated by the Satija Lab at NYGC. These methods comprise functionality not presently found in Seurat, and are able to be updated much more frequently.") (license license:gpl3)))) (define-public python-ctxcore (package (name "python-ctxcore") (version "0.2.0") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/aertslab/ctxcore") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "0nv4lc46cnzpg5gcdxrsv7b4srmkq55zl3rcadw5pn3yyz5fzd2k")))) (build-system pyproject-build-system) (arguments (list #:phases #~(modify-phases %standard-phases (add-before 'build 'pretend-version ;; The version string is usually derived via setuptools-scm, but ;; it doesn't work without the .git directory. (lambda _ (setenv "SETUPTOOLS_SCM_PRETEND_VERSION" #$version)))))) (propagated-inputs (list python-cytoolz python-frozendict python-numba python-numpy python-pandas python-pyarrow python-pyyaml python-tqdm)) (native-inputs (list python-pytest python-setuptools-scm)) (home-page "https://github.com/aertslab/ctxcore") (synopsis "Core functions for pycisTarget and the SCENIC tool suite") (description "ctxcore is part of the SCENIC suite of tools. It provides core functions for pycisTarget and SCENIC.") (license license:gpl3+))) (define-public python-arboreto (package (name "python-arboreto") (version "0.1.6") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/aertslab/arboreto") (commit "2f475dca08f47a60acc2beb8dd897e77b7495ca4"))) (file-name (git-file-name name version)) (sha256 (base32 "0l0im8ay7l2d24f7vaha454vsaha9s36bfqhbijg3b8ir8apsd7l")))) (build-system python-build-system) ;; Lots of tests fail because python-distributed fails to start the ;; "Nanny" process. (arguments '(#:tests? #false)) (propagated-inputs (list python-bokeh python-dask python-distributed python-lz4 python-numpy python-pandas python-pyarrow python-scikit-learn python-scipy python-tornado-6)) (home-page "https://github.com/aertslab/arboreto") (synopsis "Gene regulatory network inference using tree-based ensemble regressors") (description "This package implements scalable gene regulatory network inference using tree-based ensemble regressors.") (license license:bsd-3))) (define-public pyscenic ;; Latest commit from the update-pyarrow branch (let ((commit "5f170fdf474548c37ab381d1849c662820d658ee") (revision "1")) (package (name "pyscenic") (version (git-version "0.11.2" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/aertslab/pySCENIC") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "03qkvy400rjndg2ds6bhcaprir71mqr2v3yv9vd77lcnzxgw3s0z")))) (build-system pyproject-build-system) (arguments (list #:phases '(modify-phases %standard-phases ;; The cli modules referenced here have been removed, so this ;; breaks the sanity check. (add-after 'unpack 'do-not-reference-deleted-modules (lambda _ (substitute* "setup.py" (("'db2feather = .*',") "") (("'invertdb = .*',") "") (("'gmt2regions = pyscenic.cli.gmt2regions:main'") "")))) ;; Numba needs a writable dir to cache functions. (add-before 'check 'set-numba-cache-dir (lambda _ (setenv "NUMBA_CACHE_DIR" "/tmp")))))) (propagated-inputs (list python-ctxcore python-cytoolz python-multiprocessing-on-dill python-llvmlite python-numba python-attrs python-frozendict python-numpy python-pandas python-cloudpickle python-dask python-pyarrow ;XXX for dask python-distributed python-arboreto python-boltons python-setuptools python-pyyaml python-tqdm python-interlap python-umap-learn python-loompy python-networkx python-scipy python-fsspec python-requests python-aiohttp python-scikit-learn)) (native-inputs (list python-pytest)) (home-page "https://scenic.aertslab.org/") (synopsis "Single-Cell regulatory network inference and clustering") (description "pySCENIC is a Python implementation of the SCENIC pipeline (Single-Cell rEgulatory Network Inference and Clustering) which enables biologists to infer transcription factors, gene regulatory networks and cell types from single-cell RNA-seq data.") (license license:gpl3+)))) (define-public python-ikarus (package (name "python-ikarus") (version "0.0.2") (source (origin (method url-fetch) (uri (pypi-uri "ikarus" version)) (sha256 (base32 "086czpvj4yafz4vrq5rx2gy0bj2l8nzwnkk0gw8qvy4w133xjysy")))) (build-system python-build-system) (arguments `(#:tests? #false #:phases (modify-phases %standard-phases ;; See https://github.com/BIMSBbioinfo/ikarus/issues/12 (add-after 'unpack 'fix-issue-12 (lambda _ (substitute* "ikarus/classifier.py" (("pyscenic.genesig") "ctxcore.genesig")))) ;; Numba needs a writable dir to cache functions. (add-before 'check 'set-numba-cache-dir (lambda _ (setenv "NUMBA_CACHE_DIR" "/tmp")))))) (propagated-inputs (list python-numpy python-pandas python-scipy python-scanpy python-anndata python-ctxcore ;because of issue 12 pyscenic)) (home-page "https://github.com/BIMSBbioinfo/ikarus") (synopsis "Machine learning classifier of tumor cells") (description "ikarus is a stepwise machine learning pipeline that tries to cope with a task of distinguishing tumor cells from normal cells. Leveraging multiple annotated single cell datasets it can be used to define a gene set specific to tumor cells. First, the latter gene set is used to rank cells and then to train a logistic classifier for the robust classification of tumor and normal cells. Finally, sensitivity is increased by propagating the cell labels based on a custom cell-cell network. ikarus is tested on multiple single cell datasets to ascertain that it achieves high sensitivity and specificity in multiple experimental contexts.") (license license:expat))) (define-public vbz-compression (package (name "vbz-compression") (version "1.0.3") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/nanoporetech/vbz_compression/") (commit (string-append "v" version)) ;; We include the streamvbyte sources (recursive? #true))) (file-name (git-file-name name version)) (sha256 (base32 "1rn5d98flvjblhj4zjpcdqqh8qlgsh5cmb13i49fnm187p03097z")))) (build-system cmake-build-system) (arguments `(#:configure-flags '("-DENABLE_CONAN=OFF" ;; Python things aren't even installed, so we might as well ;; disable building them. "-DENABLE_PYTHON=OFF"))) (inputs (list ;("hdf5" ,hdf5-1.10) `(,zstd "lib"))) (native-inputs (list googlebenchmark)) (home-page "https://github.com/nanoporetech/vbz_compression/") (synopsis "VBZ compression plugin for nanopore signal data") (description "VBZ Compression uses variable byte integer encoding to compress nanopore signal data. The performance of VBZ is achieved by taking advantage of the properties of the raw signal and therefore is most effective when applied to the signal dataset.") (license license:mpl2.0))) (define-public python-ont-fast5-api (package (name "python-ont-fast5-api") (version "4.0.0") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/nanoporetech/ont_fast5_api") (commit (string-append "release_" version)))) (file-name (git-file-name name version)) (sha256 (base32 "01hj4751j424lzic2sc4bz1f8w7i7fpkjpy3rgghdyl5lyfyb4s4")) (modules '((guix build utils))) (snippet '(delete-file-recursively "ont_fast5_api/vbz_plugin")))) (build-system python-build-system) (arguments `(#:phases (modify-phases %standard-phases (add-after 'unpack 'copy-plugin (lambda* (#:key inputs #:allow-other-keys) (mkdir-p "ont_fast5_api/vbz_plugin/") (install-file (string-append (assoc-ref inputs "vbz-compression") "/hdf5/lib/plugin/libvbz_hdf_plugin.so") "ont_fast5_api/vbz_plugin/")))))) (inputs (list vbz-compression)) (propagated-inputs (list python-numpy python-h5py python-packaging python-progressbar33)) (home-page "https://github.com/nanoporetech/ont_fast5_api") (synopsis "Interface to HDF5 files of the Oxford Nanopore fast5 file format") (description "This package provides a concrete implementation of the fast5 file schema using the generic @code{h5py} library, plain-named methods to interact with and reflect the fast5 file schema, and tools to convert between @code{multi_read} and @code{single_read} formats.") (license license:mpl2.0))) (define-public tbsp (let ((commit "dc30c03868233c5504299c9cb0d7b2064ba9cb41") (revision "2")) (package (name "tbsp") (version (git-version "1.0.0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/phoenixding/tbsp") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "1im0bik2hxkcb7jzkcxp5nqb30hd8lfraxml6i5ik52j6z3qqln1")))) (build-system python-build-system) (arguments '(#:tests? #f ; no tests included #:phases (modify-phases %standard-phases (add-after 'unpack 'relax-requirements (lambda _ (substitute* "setup.py" ((", <3.0") ""))))))) ; matplotlib (inputs (list python-matplotlib python-networkx python-numpy python-pybigwig python-biopython-1.73 python-scikit-learn python-scipy)) (home-page "https://github.com/phoenixding/tbsp/") (synopsis "SNP-based trajectory inference") (description "Several studies focus on the inference of developmental and response trajectories from single cell RNA-Seq (scRNA-Seq) data. A number of computational methods, often referred to as pseudo-time ordering, have been developed for this task. CRISPR has also been used to reconstruct lineage trees by inserting random mutations. The tbsp package implements an alternative method to detect significant, cell type specific sequence mutations from scRNA-Seq data.") (license license:expat)))) (define-public tabixpp (package (name "tabixpp") (version "1.1.2") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/ekg/tabixpp") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "00aqs147yn8zcvxims5njwxqsbnlbjv7lnmiwqy80bfdcbhljkqf")) (modules '((guix build utils))) (snippet '(delete-file-recursively "htslib")))) (build-system gnu-build-system) (inputs (list bzip2 curl htslib xz zlib)) (arguments (list #:make-flags #~(list (string-append "CC=" #$(cc-for-target)) (string-append "CXX=" #$(cxx-for-target)) "HTS_HEADERS=" (string-append "HTS_LIB=" (search-input-file %build-inputs "/lib/libhts.a")) "INCLUDES=") #:tests? #f ; There are no tests to run. #:phases #~(modify-phases %standard-phases (delete 'configure) ; There is no configure phase. ;; Build shared and static libraries. (add-after 'build 'build-libraries (lambda* (#:key inputs #:allow-other-keys) (invoke #$(cxx-for-target) "-shared" "-o" "libtabixpp.so" "tabix.o" "-lhts") (invoke #$(ar-for-target) "rcs" "libtabixpp.a" "tabix.o"))) (replace 'install (lambda _ (let ((lib (string-append #$output "/lib")) (bin (string-append #$output "/bin"))) (install-file "tabix++" bin) (install-file "libtabixpp.so" lib) (install-file "libtabixpp.a" lib) (install-file "tabix.hpp" (string-append #$output "/include")) (mkdir-p (string-append lib "/pkgconfig")) (with-output-to-file (string-append lib "/pkgconfig/tabixpp.pc") (lambda _ (format #t "\ prefix=~a~@ exec_prefix=${prefix}~@ libdir=${exec_prefix}/lib~@ includedir=${prefix}/include~@ ~@ ~@ Name: libtabixpp~@ Version: ~a~@ Description: C++ wrapper around tabix project~@ Libs: -L${libdir} -ltabixpp~@ Cflags: -I${includedir}~%" #$output #$version))))))))) (home-page "https://github.com/ekg/tabixpp") (synopsis "C++ wrapper around tabix project") (description "This is a C++ wrapper around the Tabix project which abstracts some of the details of opening and jumping in tabix-indexed files.") (license license:expat))) (define-public smithwaterman (let ((commit "2610e259611ae4cde8f03c72499d28f03f6d38a7")) (package (name "smithwaterman") (version (git-version "0.0.0" "2" commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/ekg/smithwaterman/") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0i9d8zrxpiracw3mxzd9siybpy62p06rqz9mc2w93arajgbk45bs")))) (build-system gnu-build-system) (arguments (list #:tests? #f ; There are no tests to run. #:make-flags #~(list (string-append "CXX=" #$(cxx-for-target)) "libsw.a" "all") #:phases #~(modify-phases %standard-phases (delete 'configure) ; There is no configure phase. (add-after 'unpack 'patch-source (lambda _ (substitute* "Makefile" (("-c ") "-c -fPIC ")) #$@(if (%current-target-system) #~((substitute* "Makefile" (("\tld") (string-append "\t" #$(%current-target-system) "-ld")) (("\tar") (string-append "\t" #$(%current-target-system) "-ar")))) '()))) (add-after 'build 'build-dynamic (lambda _ (invoke #$(cxx-for-target) "-shared" "-o" "libsmithwaterman.so" "smithwaterman.o" "SmithWatermanGotoh.o" "disorder.o" "BandedSmithWaterman.o" "LeftAlign.o" "Repeats.o" "IndelAllele.o"))) (replace 'install (lambda* (#:key outputs #:allow-other-keys) (let* ((out (assoc-ref outputs "out")) (bin (string-append out "/bin")) (lib (string-append out "/lib"))) (install-file "smithwaterman" bin) (for-each (lambda (file) (install-file file (string-append out "/include/smithwaterman"))) (find-files "." "\\.h$")) (install-file "libsmithwaterman.so" lib) (install-file "libsw.a" lib) (mkdir-p (string-append lib "/pkgconfig")) (with-output-to-file (string-append lib "/pkgconfig/smithwaterman.pc") (lambda _ (format #t "prefix=~a~@ exec_prefix=${prefix}~@ libdir=${exec_prefix}/lib~@ includedir=${prefix}/include/smithwaterman~@ ~@ ~@ Name: smithwaterman~@ Version: ~a~@ Description: smith-waterman-gotoh alignment algorithm~@ Libs: -L${libdir} -lsmithwaterman~@ Cflags: -I${includedir}~%" out #$version))))))))) (home-page "https://github.com/ekg/smithwaterman") (synopsis "Implementation of the Smith-Waterman algorithm") (description "Implementation of the Smith-Waterman algorithm.") ;; The licensing terms are unclear: https://github.com/ekg/smithwaterman/issues/9. (license (list license:gpl2 license:expat))))) (define-public sylamer (package (name "sylamer") (version "18-131") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/micans/sylamer/") (commit "aa75c3584797c0c15f860addb645f7bc1dd7627d"))) (file-name (git-file-name name version)) (sha256 (base32 "1ddiwlrdghhb4574rvfw0brjp9gs5l6nfsy82h0m4mvz1dr3gkj5")))) (build-system gnu-build-system) (arguments (list #:tests? #f ; no test target #:make-flags #~(list (string-append "GSLPREFIX=" #$(this-package-input "gsl"))) #:phases '(modify-phases %standard-phases (replace 'configure (lambda* (#:key outputs #:allow-other-keys) (substitute* "Makefile" (("cp sylamer \\$\$HOME\$/local/bin") (string-append "install -D -t " (assoc-ref outputs "out") "/bin sylamer"))) (install-file "Makefile" "src") (chdir "src")))))) (inputs (list gsl zlib)) (home-page "https://www.ebi.ac.uk/research/enright/software/sylamer") (synopsis "Asses microRNA binding and siRNA off-target effects") (description "Sylamer is a system for finding significantly over or under-represented words in sequences according to a sorted gene list. Typically it is used to find significant enrichment or depletion of microRNA or siRNA seed sequences from microarray expression data. Sylamer is extremely fast and can be applied to genome-wide datasets with ease. Results are plotted in terms of a significance landscape plot. These plots show significance profiles for each word studied across the sorted genelist.") (license license:gpl3+))) (define-public multichoose (package (name "multichoose") (version "1.0.3") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/ekg/multichoose/") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "0ci5fqvmpamwgxvmyd79ygj6n3bnbl3vc7b6h1sxz58186sm3pfs")))) (build-system gnu-build-system) (arguments (list #:tests? #f ;Tests require node. #:phases #~(modify-phases %standard-phases (delete 'configure) ;There is no configure phase. (replace 'install (lambda _ (let ((bin (string-append #$output "/bin")) (include (string-append #$output "/include"))) ;; TODO: There are Python modules for these programs too. (install-file "multichoose" bin) (install-file "multipermute" bin) (install-file "multichoose.h" include) (install-file "multipermute.h" include))))))) (home-page "https://github.com/ekg/multichoose") (synopsis "Efficient loopless multiset combination generation algorithm") (description "This library implements an efficient loopless multiset combination generation algorithm which is (approximately) described in \"Loopless algorithms for generating permutations, combinations, and other combinatorial configurations.\", G. Ehrlich - Journal of the ACM (JACM), 1973. (Algorithm 7.)") (license license:expat))) (define-public fsom (let ((commit "a6ef318fbd347c53189384aef7f670c0e6ce89a3")) (package (name "fsom") (version (git-version "0.0.0" "1" commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/ekg/fsom/") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0gw1lpvr812pywg9y546x0h1hhj261xwls41r6kqhddjlrcjc0pi")))) (build-system gnu-build-system) (arguments `(#:tests? #f ; There are no tests to run. #:phases (modify-phases %standard-phases (delete 'configure) ; There is no configure phase. (replace 'install (lambda* (#:key outputs #:allow-other-keys) (let ((bin (string-append (assoc-ref outputs "out") "/bin"))) (install-file "fsom" bin))))))) (native-inputs (list gcc-6)) (home-page "https://github.com/ekg/fsom") (synopsis "Manage SOM (Self-Organizing Maps) neural networks") (description "A tiny C library for managing SOM (Self-Organizing Maps) neural networks.") (license license:gpl3)))) (define-public fastahack (package (name "fastahack") (version "1.0.0") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/ekg/fastahack/") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "0rp1blskhzxf7vbh253ibpxbgl9wwgyzf1wbkxndi08d3j4vcss9")))) (build-system gnu-build-system) (arguments (list #:make-flags #~(list (string-append "CXX=" #$(cxx-for-target))) ;; Unclear how to run tests: https://github.com/ekg/fastahack/issues/15 #:tests? #f #:phases #~(modify-phases %standard-phases (delete 'configure) ; There is no configure phase. (add-after 'unpack 'patch-source (lambda _ (substitute* "Makefile" (("-c ") "-c -fPIC ")))) (add-after 'build 'build-dynamic (lambda _ (invoke #$(cxx-for-target) "-shared" "-o" "libfastahack.so" "Fasta.o" "FastaHack.o" "split.o" "disorder.o"))) (replace 'install (lambda* (#:key outputs #:allow-other-keys) (let* ((out (assoc-ref outputs "out")) (lib (string-append out "/lib")) (bin (string-append out "/bin"))) (mkdir-p (string-append out "/include/fastahack")) (for-each (lambda (file) (install-file file (string-append out "/include/fastahack"))) (find-files "." "\\.h$")) (install-file "fastahack" bin) (install-file "libfastahack.so" lib) (mkdir-p (string-append lib "/pkgconfig")) (with-output-to-file (string-append lib "/pkgconfig/fastahack.pc") (lambda _ (format #t "prefix=~a~@ exec_prefix=${prefix}~@ libdir=${exec_prefix}/lib~@ includedir=${prefix}/include/fastahack~@ ~@ ~@ Name: fastahack~@ Version: ~a~@ Description: Indexing and sequence extraction from FASTA files~@ Libs: -L${libdir} -lfastahack~@ Cflags: -I${includedir}~%" out #$version))))))))) (home-page "https://github.com/ekg/fastahack") (synopsis "Indexing and sequence extraction from FASTA files") (description "Fastahack is a small application for indexing and extracting sequences and subsequences from FASTA files. The included library provides a FASTA reader and indexer that can be embedded into applications which would benefit from directly reading subsequences from FASTA files. The library automatically handles index file generation and use.") (license (list license:expat license:gpl2)))) (define-public wfa2-lib (package (name "wfa2-lib") (version "2.3.3") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/smarco/WFA2-lib") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "110s1s79z8ndjs4qdgmrj708iiaqyagia3gi2fxak101lg263diw")))) (build-system cmake-build-system) (arguments (list #:phases #~(modify-phases %standard-phases ;; This pkg-config file is provided by other distributions. (add-after 'install 'install-pkg-config-file (lambda _ (let ((pkgconfig (string-append #$output "/lib/pkgconfig"))) (mkdir-p pkgconfig) (with-output-to-file (string-append pkgconfig "/libwfa2.pc") (lambda _ (format #t "\ prefix=~a~@ exec_prefix=${prefix}~@ libdir=${exec_prefix}/lib~@ includedir=${prefix}/include/wfa2lib~@ ~@ Name: libwfa2~@ Version: ~a~@ Description: Wavefront alignment algorithm library~@ Libs: -L${libdir} -lwfa2 -lwfa2cpp~@ Cflags: -I${includedir}~%" #$output #$version))))))))) (native-inputs (list pkg-config)) (home-page "https://github.com/smarco/WFA2-lib") (synopsis "Wavefront alignment algorithm library") (description "The wavefront alignment (WFA) algorithm is an exact gap-affine algorithm that takes advantage of homologous regions between the sequences to accelerate the alignment process.") (properties `((tunable? . #t))) (license license:expat))) (define-public vcflib (package (name "vcflib") (version "1.0.9") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/vcflib/vcflib") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "0cmznzq7hl5vr504ww262rwz5lfdfrca5ksbcvwh3cgp44fiwykv")) (modules '((guix build utils))) (snippet #~(begin (substitute* "CMakeLists.txt" ((".*fastahack.*") "") ((".*smithwaterman.*") "") (("(pkg_check_modules\\(TABIXPP)" text) (string-append "pkg_check_modules(WFA2 REQUIRED libwfa2)\n" "pkg_check_modules(FASTAHACK REQUIRED fastahack)\n" "pkg_check_modules(SMITHWATERMAN REQUIRED smithwaterman)\n" text)) (("\\$\\{TABIXPP_LIBRARIES\\}" text) (string-append "${FASTAHACK_LIBRARIES} " "${WFA2_LIBRARIES} " "${SMITHWATERMAN_LIBRARIES} " text))) (substitute* (find-files "." "\\.(h|c)(pp)?$") (("\"SmithWatermanGotoh.h\"") "<smithwaterman/SmithWatermanGotoh.h>") (("\"convert.h\"") "<smithwaterman/convert.h>") (("\"disorder.h\"") "<smithwaterman/disorder.h>") (("\"wavefront/wfa.hpp\"") "<wavefront/wfa.hpp>") (("Fasta.h") "fastahack/Fasta.h")))))) (build-system cmake-build-system) (inputs (list bzip2 curl htslib fastahack perl python pybind11 smithwaterman tabixpp xz zlib)) (propagated-inputs (list wfa2-lib)) (native-inputs `(("pkg-config" ,pkg-config) ;; Submodules. ;; This package builds against the .o files so we need to extract the source. ("filevercmp-src" ,(package-source filevercmp)) ("fsom-src" ,(package-source fsom)) ("intervaltree-src" ,(package-source intervaltree)) ("multichoose-src" ,(package-source multichoose)))) (arguments (list #:configure-flags #~(list "-DZIG=OFF" "-DTABIXPP_LOCAL=OFF" "-DTABIX_FOUND=ON" "-DWFA_GITMODULE=OFF" (string-append "-DPKG_CONFIG_EXECUTABLE=" (search-input-file %build-inputs (string-append "/bin/" #$(pkg-config-for-target))))) #:tests? #f ; no tests #:phases #~(modify-phases %standard-phases (add-after 'unpack 'find-wfa2lib-headers (lambda _ (setenv "CPLUS_INCLUDE_PATH" (string-append #$(this-package-input "wfa2-lib") "/include/wfa2lib:" (or (getenv "CPLUS_INCLUDE_PATH") ""))))) (add-after 'unpack 'build-shared-library (lambda _ (substitute* "CMakeLists.txt" (("vcflib STATIC") "vcflib SHARED")))) (add-after 'unpack 'unpack-submodule-sources (lambda* (#:key inputs native-inputs #:allow-other-keys) (let ((unpack (lambda (source target) (mkdir-p target) (with-directory-excursion target (let ((source (or (assoc-ref inputs source) (assoc-ref native-inputs source)))) (if (file-is-directory? source) (copy-recursively source ".") (invoke "tar" "xvf" source "--strip-components=1"))))))) (and (unpack "filevercmp-src" "contrib/filevercmp") (unpack "fsom-src" "contrib/fsom") (unpack "intervaltree-src" "contrib/intervaltree") (unpack "multichoose-src" "contrib/multichoose")) ;; This is needed for downstream packages to allow building ;; with GCC 11+. (substitute* "contrib/intervaltree/IntervalTree.h" (("#include <vector>" m) (string-append m " #include <limits> /* std::numeric_limits */")))))) ;; This pkg-config file is provided by other distributions. (add-after 'install 'install-pkg-config-file (lambda _ (let ((pkgconfig (string-append #$output "/lib/pkgconfig"))) (mkdir-p pkgconfig) (with-output-to-file (string-append pkgconfig "/vcflib.pc") (lambda _ (format #t "\ prefix=~a~@ exec_prefix=${prefix}~@ libdir=${exec_prefix}/lib~@ includedir=${prefix}/include~@ ~@ Name: vcflib~@ Version: ~a~@ Requires: libwfa2, smithwaterman, fastahack, tabixpp~@ Description: C++ library for parsing and manipulating VCF files~@ Libs: -L${libdir} -lvcflib~@ Cflags: -I${includedir}~%" #$output #$version))))))))) (home-page "https://github.com/vcflib/vcflib/") (synopsis "Library for parsing and manipulating VCF files") (description "Vcflib provides methods to manipulate and interpret sequence variation as it can be described by VCF. It is both an API for parsing and operating on records of genomic variation as it can be described by the VCF format, and a collection of command-line utilities for executing complex manipulations on VCF files.") (license license:expat))) (define-public freebayes (package (name "freebayes") (version "1.3.7") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/freebayes/freebayes") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "163nd1xkq547za80khlys4qkgal64f3sgl6ap3yvik68r0rgyisv")))) (build-system meson-build-system) (inputs (list fastahack htslib smithwaterman tabixpp vcflib)) (native-inputs `(("bash-tap" ,bash-tap) ("bc" ,bc) ("grep" ,grep) ; Built with perl support. ("parallel" ,parallel) ("perl" ,perl) ("pkg-config" ,pkg-config) ("python" ,python) ("samtools" ,samtools) ("simde" ,simde) ;; This submodule is needed to run the tests. ("test-simple-bash-src" ,(origin (method git-fetch) (uri (git-reference (url "https://github.com/ingydotnet/test-simple-bash/") (commit "124673ff204b01c8e96b7fc9f9b32ee35d898acc"))) (file-name "test-simple-bash-src-checkout") (sha256 (base32 "043plp6z0x9yf7mdpky1fw7zcpwn1p47px95w9mh16603zqqqpga")))))) (arguments `(#:phases (modify-phases %standard-phases (add-after 'unpack 'patch-source (lambda* (#:key inputs #:allow-other-keys) (let ((bash-tap (assoc-ref inputs "bash-tap"))) (substitute* (find-files "test/t") (("BASH_TAP_ROOT=bash-tap") (string-append "BASH_TAP_ROOT=" bash-tap "/bin")) (("bash-tap/bash-tap-bootstrap") (string-append bash-tap "/bin/bash-tap-bootstrap")) (("source.*bash-tap-bootstrap") (string-append "source " bash-tap "/bin/bash-tap-bootstrap"))) (substitute* '("src/BedReader.cpp" "src/BedReader.h") (("../intervaltree/IntervalTree.h") "IntervalTree.h")) ;; We don't have Perl support in grep -E. (substitute* '("test/t/01_call_variants.t" "test/t/01b_call_variants.t") (("grep -P") "grep -E") (("\\\\t") " ")) (substitute* "meson.build" ;; Our pkg-config file is vcflib.pc (("libvcflib") "vcflib") (("vcflib_inc,") ""))))) (add-after 'unpack 'unpack-submodule-sources (lambda* (#:key inputs #:allow-other-keys) (mkdir-p "test/test-simple-bash") (copy-recursively (assoc-ref inputs "test-simple-bash-src") "test/test-simple-bash"))) ;; The slow tests take longer than the specified timeout. ,@(if (any (cute string=? <> (%current-system)) '("armhf-linux" "aarch64-linux")) '((replace 'check (lambda* (#:key tests? #:allow-other-keys) (when tests? (invoke "meson" "test" "--timeout-multiplier" "5"))))) '())))) (home-page "https://github.com/freebayes/freebayes") (synopsis "Haplotype-based variant detector") (description "FreeBayes is a Bayesian genetic variant detector designed to find small polymorphisms, specifically SNPs (single-nucleotide polymorphisms), indels (insertions and deletions), MNPs (multi-nucleotide polymorphisms), and complex events (composite insertion and substitution events) smaller than the length of a short-read sequencing alignment.") (license license:expat))) (define-public samblaster (package (name "samblaster") (version "0.1.26") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/GregoryFaust/samblaster") (commit (string-append "v." version)))) (file-name (git-file-name name version)) (sha256 (base32 "0g24fq5hplnfgqkh3xqpg3lgx3wmxwnh9c7m6yw7pbi40lmgl1jv")))) (build-system gnu-build-system) (arguments (list #:tests? #f ;there are none #:phases #~(modify-phases %standard-phases (delete 'configure) ;There is no configure phase. (replace 'install (lambda _ (install-file "samblaster" (string-append #$output "/bin"))))))) (home-page "https://github.com/GregoryFaust/samblaster") (synopsis "Mark duplicates in paired-end SAM files") (description "Samblaster is a fast and flexible program for marking duplicates in read-id grouped paired-end SAM files. It can also optionally output discordant read pairs and/or split read mappings to separate SAM files, and/or unmapped/clipped reads to a separate FASTQ file. When marking duplicates, samblaster will require approximately 20MB of memory per 1M read pairs.") (license license:expat))) (define-public r-velocyto (let ((commit "d7790346cb99f49ab9c2b23ba70dcf9d2c9fc350") (revision "1")) (package (name "r-velocyto") (version (git-version "0.6" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/velocyto-team/velocyto.R") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "16wqf70j7rd7pay2q513iyz12i8n9vrpg1bisah4lddbcpx5dz1n")))) (build-system r-build-system) (inputs (list boost)) (propagated-inputs (list r-hdf5r r-mass r-mgcv r-pcamethods r-rcpp r-rcpparmadillo ;; Suggested packages r-rtsne r-cluster r-abind r-h5 r-biocgenerics r-genomicalignments r-rsamtools r-edger r-igraph)) (home-page "https://velocyto.org") (synopsis "RNA velocity estimation in R") (description "This package provides basic routines for estimation of gene-specific transcriptional derivatives and visualization of the resulting velocity patterns.") (license license:gpl3)))) (define-public r-voltron (let ((commit "5057b703479239a9aaba761f07e65d849f6111f8") (revision "1")) (package (name "r-voltron") (version (git-version "1.0.0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/BIMSBbioinfo/VoltRon") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "1nximl4708a7fdwn8ysxpni3mp6dx33cphavlay7hh1pa55pnzgn")) (modules '((guix build utils))) ;; The tripack package is not available under a free license, ;; but interp provides free implementations of "tri.mesh" and ;; "neighbours". (snippet '(substitute* '("DESCRIPTION" "NAMESPACE" "R/spatial.R") (("tripack") "interp"))))) (properties `((upstream-name . "VoltRon"))) (build-system r-build-system) (inputs (list opencv tbb zlib)) (propagated-inputs (list r-anndata r-data-table r-dplyr r-ebimage r-fastdummies r-fnn r-ggforce r-ggplot2 r-ggpubr r-ggrepel r-hdf5r r-htmltools r-igraph r-interp r-irlba r-magick r-matrix r-morpho r-raster r-rcpp r-reshape2 r-rjson r-rlang r-s4vectors r-scales r-shiny r-shinyjs r-stringr r-terra r-umap r-xml)) (native-inputs (list pkg-config)) (home-page "https://github.com/BIMSBbioinfo/VoltRon") (synopsis "VoltRon for Spatial Data Integration and Analysis") (description "@code{VoltRon} is a toolbox for spatial data analysis, multi-omics integration using spatial image registration. @code{VoltRon} is capable of analyzing multiple types and modalities of spatially-aware datasets. @code{VoltRon} visualizes and analyzes regions of interests (ROIs), spots, cells and even molecules.") (license license:expat)))) (define-public methyldackel (package (name "methyldackel") (version "0.6.1") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/dpryan79/MethylDackel") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "06kj76pyhzxfcjcpm840a3km3fa9994kfq4asglnb228pwak326z")))) (build-system gnu-build-system) (arguments (list #:test-target "test" #:make-flags #~(list "CC=gcc" "CFLAGS=-fcommon" "LIBBIGWIG=-lBigWig" (string-append "prefix=" #$output "/bin/")) #:phases '(modify-phases %standard-phases (replace 'configure (lambda _ (substitute* "Makefile" (("install MethylDackel \\$\$prefix\$" match) (string-append "install -d $(prefix); " match)))))))) (inputs (list curl htslib libbigwig zlib)) ;; Needed for tests (native-inputs (list python-wrapper)) (home-page "https://github.com/dpryan79/MethylDackel") (synopsis "Universal methylation extractor for BS-seq experiments") (description "MethylDackel will process a coordinate-sorted and indexed BAM or CRAM file containing some form of BS-seq alignments and extract per-base methylation metrics from them. MethylDackel requires an indexed fasta file containing the reference genome as well.") ;; See https://github.com/dpryan79/MethylDackel/issues/85 (license license:expat))) ;; This package bundles PCRE 8.02 and cannot be built with the current ;; version. (define-public phast (package (name "phast") (version "1.5") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/CshlSiepelLab/phast") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "10lpbllvny923jjbbyrpxahhd1m5h7sbj9gx7rd123rg10mlidki")))) (build-system gnu-build-system) (arguments (list #:make-flags #~(list "CC=gcc" (string-append "DESTDIR=" #$output)) #:phases #~(modify-phases %standard-phases (replace 'configure (lambda* (#:key inputs outputs #:allow-other-keys) ;; Fix syntax (substitute* "test/Makefile" ((" ") " ")) (substitute* "Makefile" (("CLAPACKPATH=/usr/lib") (string-append "CLAPACKPATH=" #$(this-package-input "clapack") "/lib"))) ;; Renaming the libraries is not necessary with our version of ;; CLAPACK. (substitute* "src/lib/Makefile" (("ifdef CLAPACKPATH") "ifdef UNNECESSARY")) (substitute* "src/make-include.mk" (("-lblaswr") "-lblas") (("-ltmg") "-ltmglib") (("liblapack.a") "liblapack.so") (("libblas.a") "libblas.so") (("libf2c.a") "libf2c.so")) (substitute* "src/Makefile" (("/opt") "/share") (("/usr/") "/")))) (replace 'check (lambda _ (setenv "PATH" (string-append (getcwd) "/bin:" (getenv "PATH"))) ;; Disable broken test (substitute* "test/Makefile" ((".*if.*hmrc_summary" m) (string-append "#" m))) ;; Only run the msa_view tests because the others fail for ;; unknown reasons. (invoke "make" "-C" "test" "msa_view")))))) (inputs (list clapack)) (native-inputs (list perl)) (home-page "http://compgen.cshl.edu/phast/") (synopsis "Phylogenetic analysis with space/time models") (description "Phylogenetic Analysis with Space/Time models (PHAST) is a collection of command-line programs and supporting libraries for comparative and evolutionary genomics. Best known as the search engine behind the Conservation tracks in the University of California, Santa Cruz (UCSC) Genome Browser, PHAST also includes several tools for phylogenetic modeling, functional element identification, as well as utilities for manipulating alignments, trees and genomic annotations.") (license license:bsd-3))) (define-public python-gffutils (package (name "python-gffutils") (version "0.10.1") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/daler/gffutils") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "1gkzk7ps6w3ai2r81js9s9bzpba0jmxychnd2da6n9ggdnf2xzqz")))) (build-system python-build-system) (arguments '(#:phases (modify-phases %standard-phases (replace 'check (lambda* (#:key tests? #:allow-other-keys) (when tests? ;; Tests need to access the HOME directory (setenv "HOME" "/tmp") (invoke "nosetests" "-a" "!slow"))))))) (propagated-inputs (list python-argcomplete python-argh python-biopython python-pybedtools python-pyfaidx python-simplejson python-six)) (native-inputs (list python-nose)) (home-page "https://github.com/daler/gffutils") (synopsis "Tool for manipulation of GFF and GTF files") (description "python-gffutils is a Python package for working with and manipulating the GFF and GTF format files typically used for genomic annotations. The files are loaded into a SQLite database, allowing much more complex manipulation of hierarchical features (e.g., genes, transcripts, and exons) than is possible with plain-text methods alone.") (license license:expat))) (define-public indelfixer (package (name "indelfixer") (version "1.1") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/cbg-ethz/InDelFixer/") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "10ak05x8i1bx2p7rriv2rglqg1wr7c8wrhjrqlq1wm7ka99w8i79")))) (build-system ant-build-system) (arguments `(#:jar-name "InDelFixer.jar" #:source-dir "src/main/java" #:test-dir "src/test")) (inputs `(("java-commons-lang2" ,java-commons-lang) ("java-args4j" ,java-args4j))) (native-inputs (list java-junit)) (home-page "https://github.com/cbg-ethz/InDelFixer/") (synopsis "Iterative and sensitive NGS sequence aligner") (description "InDelFixer is a sensitive aligner for 454, Illumina and PacBio data, employing a full Smith-Waterman alignment against a reference. This Java command line application aligns Next-Generation Sequencing (NGS) and third-generation reads to a set of reference sequences, by a prior fast k-mer matching and removes indels, causing frame shifts. In addition, only a specific region can be considered. An iterative refinement of the alignment can be performed, by alignment against the consensus sequence with wobbles. The output is in SAM format.") (license license:gpl3+))) (define-public libsbml (package (name "libsbml") (version "5.18.0") (source (origin (method url-fetch) (uri (string-append "mirror://sourceforge/sbml/libsbml/" version "/stable/libSBML-" version "-core-src.tar.gz")) (sha256 (base32 "0slkagrk3nfi2qsksv6b1brj6zhx4bj4bkib2sdycvrcd10ql2lh")))) (build-system cmake-build-system) (arguments `(#:test-target "test" #:configure-flags ,#~(list "-DWITH_CHECK=ON" (string-append "-DLIBXML_LIBRARY=" #$(this-package-input "libxml2") "/lib/libxml2.so") (string-append "-DLIBXML_INCLUDE_DIR=" #$(this-package-input "libxml2") "/include/libxml2")))) (propagated-inputs (list libxml2)) (native-inputs (list check swig)) (home-page "https://sbml.org/Software/libSBML") (synopsis "Process SBML files and data streams") (description "LibSBML is a library to help you read, write, manipulate, translate, and validate SBML files and data streams. The @dfn{Systems Biology Markup Language} (SBML) is an interchange format for computer models of biological processes. SBML is useful for models of metabolism, cell signaling, and more. It continues to be evolved and expanded by an international community.") (license license:lgpl2.1+))) (define-public kraken2 (package (name "kraken2") (version "2.1.2") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/DerrickWood/kraken2") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "1pl6ml1ldg2hnhy8ps56q0fl1wq3g91qkhinj6pb4yjjhv1rxsjf")))) (build-system gnu-build-system) (arguments `(#:tests? #false ; there are none #:make-flags ,#~(list "-C" "src" (string-append "KRAKEN2_DIR=" #$output "/bin")) #:phases (modify-phases %standard-phases (delete 'configure) (add-before 'install 'install-scripts (lambda* (#:key outputs #:allow-other-keys) (let* ((bin (string-append (assoc-ref outputs "out") "/bin")) (replacements `(("KRAKEN2_DIR" . ,bin) ("VERSION" . ,,version)))) (mkdir-p bin) (with-directory-excursion "scripts" (let ((scripts (find-files "." ".*"))) (substitute* scripts (("#####=([^=]+)=#####" _ key) (or (assoc-ref replacements key) (error (format #false "unknown key: ~a~%" key))))) (substitute* "kraken2" (("compression_program = \"bzip2\"") (string-append "compression_program = \"" (which "bzip2") "\"")) (("compression_program = \"gzip\"") (string-append "compression_program = \"" (which "gzip") "\""))) (substitute* '("download_genomic_library.sh" "download_taxonomy.sh" "16S_gg_installation.sh" "16S_silva_installation.sh" "16S_rdp_installation.sh") (("wget") (which "wget"))) (substitute* '("download_taxonomy.sh" "download_genomic_library.sh" "rsync_from_ncbi.pl") (("rsync -") (string-append (which "rsync") " -"))) (substitute* "mask_low_complexity.sh" (("which") (which "which"))) (substitute* '("mask_low_complexity.sh" "download_genomic_library.sh" "16S_silva_installation.sh") (("sed -e ") (string-append (which "sed") " -e "))) (substitute* '("rsync_from_ncbi.pl" "16S_rdp_installation.sh" "16S_silva_installation.sh" "16S_gg_installation.sh" "download_taxonomy.sh" "download_genomic_library.sh") (("gunzip") (which "gunzip"))) (for-each (lambda (script) (chmod script #o555) (install-file script bin)) scripts))))))))) (inputs (list gzip perl rsync sed wget which)) (home-page "https://github.com/DerrickWood/kraken2") (synopsis "Taxonomic sequence classification system") (description "Kraken is a taxonomic sequence classifier that assigns taxonomic labels to DNA sequences. Kraken examines the k-mers within a query sequence and uses the information within those k-mers to query a database. That database maps k-mers to the lowest common ancestor (LCA) of all genomes known to contain a given k-mer.") (license license:expat))) (define-public lofreq (package (name "lofreq") (version "2.1.5") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/CSB5/lofreq") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "0qssrn3mgjak7df6iqc1rljqd3g3a5syvg0lsv4vds43s3fq23bl")))) (build-system gnu-build-system) (arguments '(#:test-target "bug-tests" #:tests? #false ;test data are not included #:phases (modify-phases %standard-phases (add-after 'unpack 'set-source-file-times-to-1980 (lambda _ (let ((circa-1980 (* 10 366 24 60 60))) (for-each (lambda (file) (let ((s (lstat file))) (unless (eq? (stat:type s) 'symlink) (utime file circa-1980 circa-1980)))) (find-files "." #:directories? #t)))))))) (inputs (list htslib python-wrapper zlib)) (native-inputs (list autoconf automake which)) (home-page "https://csb5.github.io/lofreq/") (synopsis "Sensitive variant calling from sequencing data") (description "LoFreq is a fast and sensitive variant-caller for inferring SNVs and indels from next-generation sequencing data. It makes full use of base-call qualities and other sources of errors inherent in sequencing (e.g. mapping or base/indel alignment uncertainty), which are usually ignored by other methods or only used for filtering.") (license license:expat))) (define-public louvain (package (name "louvain") (version "0.2") (source (origin (method url-fetch) (uri "mirror://sourceforge/louvain/louvain_latest.tar.gz") (sha256 (base32 "0hqlv5jqc889nbv7j1bchrx4zhh69hgr2mqvfdygc7kwrywn22lb")))) (build-system gnu-build-system) (arguments (list #:tests? #false ;there are none #:phases #~(modify-phases %standard-phases (delete 'configure) (add-after 'unpack 'patch-includes (lambda _ (substitute* "main_community.cpp" (("using namespace std;" m) (string-append "#include <unistd.h> /* for getpid */\n" m))))) (replace 'install (lambda _ (for-each (lambda (exe) (install-file exe (string-append #$output "/bin"))) '("convert" "community" "hierarchy"))))))) (home-page "https://sourceforge.net/projects/louvain/") (synopsis "Multi-criteria community detection") (description "This package offers a set of functions to use in order to compute communities on graphs weighted or unweighted.") (license license:gpl3+))) (define-public ivar (package (name "ivar") (version "1.4.2") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/andersen-lab/ivar") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "0v3rsak84ilg4iaynwpmmkj507vham5rjk2pfsmylpaqylgc69yx")))) (build-system gnu-build-system) (arguments (list #:parallel-tests? #false ;not supported #:phases '(modify-phases %standard-phases (add-after 'unpack 'patch-CXXFLAGS (lambda _ (substitute* '("src/Makefile.am" "tests/Makefile.am") (("-Werror") ""))))))) (inputs (list htslib zlib)) (native-inputs (list autoconf automake)) (home-page "https://andersen-lab.github.io/ivar/html/") (synopsis "Tools for amplicon-based sequencing") (description "iVar is a computational package that contains functions broadly useful for viral amplicon-based sequencing.") (license license:gpl3+))) (define-public python-pyliftover (package (name "python-pyliftover") (version "0.4") ;; The version of pypi does not include test data. (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/konstantint/pyliftover") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "1j8jp9iynv2l3jv5pr0pn0p3azlama1bqg233piglzm6bqh3m2m3")))) (build-system python-build-system) (arguments `(#:tests? #false)) ; the tests access the web (native-inputs (list python-pytest)) (home-page "https://github.com/konstantint/pyliftover") (synopsis "Python implementation of UCSC liftOver genome coordinate conversion") (description "PyLiftover is a library for quick and easy conversion of genomic (point) coordinates between different assemblies.") (license license:expat))) (define-public python-cgatcore (package (name "python-cgatcore") (version "0.6.15") ;; The version of pypi does not include test data. (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/cgat-developers/cgat-core") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "103hpdnkqr3a34blbicshk56j36g652s0g1zi9isppc5dngn0s18")))) (build-system pyproject-build-system) (arguments (list #:test-flags '(list "-k" (string-append ;; This test actually does what it should, but the check fails with ;; TypeError: cannot unpack non-iterable Namespace object "not test_start_and_stop_are_logged_with_argparse" ;; These all attempt to connect to localhost with SSH " and not test_job_should_use_TMPDIR_and_clean_up" " and not test_job_should_use_TMPDIR_and_clean_up_after_fail" " and not test_job_should_write_to_explicit_temp_and_not_clean_up")) #:phases '(modify-phases %standard-phases (add-after 'unpack 'fix-references (lambda _ (substitute* "cgatcore/pipeline/execution.py" (("#!/bin/bash") (string-append "#!" (which "bash"))) (("executable=\"/bin/bash\"") (string-append "executable=\"" (which "bash") "\"")) (("\\\\time") (which "time"))))) (add-after 'unpack 'sqlite-compatibility (lambda _ ;; Load apsw (and thus newer sqlite3) before importing Python's ;; older sqlite3 library. (substitute* "cgatcore/pipeline/__init__.py" (("import os") (string-append "import os\nimport apsw"))) (substitute* "tests/template_pipeline.py" (("import sys" m) (string-append "import apsw\n" m)))))))) (native-inputs (list python-pytest lsof inetutils openssl)) (inputs (list time)) (propagated-inputs (list python-apsw python-gevent python-pandas python-paramiko python-pyyaml python-ruffus python-sqlalchemy)) (home-page "https://github.com/cgat-developers/cgat-core") (synopsis "Computational genomics analysis toolkit") (description "CGAT-core is a set of libraries and helper functions used to enable researchers to design and build computational workflows for the analysis of large-scale data-analysis.") (license license:expat))) (define-public perl-cworld-dekker (package (name "perl-cworld-dekker") (version "1.01") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/dekkerlab/cworld-dekker.git") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "1dvh23fx52m59y6304xi2j2pl2hiqadlqg8jyv2pm14j1hy71ych")))) (build-system perl-build-system) (arguments (list #:modules '((guix build perl-build-system) (guix build utils) (srfi srfi-26)) #:phases #~(modify-phases %standard-phases (add-after 'unpack 'hardcode-references (lambda* (#:key inputs #:allow-other-keys) (let ((bedtools #$(this-package-input "bedtools")) (r #$(this-package-input "r-minimal"))) (substitute* '("scripts/python/getEigenVectors.py" "scripts/python/matrix2EigenVectors.py") (("bedtools intersect") (string-append bedtools "/bin/bedtools intersect"))) (substitute* "lib/cworld/dekker.pm" (("bedtools --version") (string-append bedtools "/bin/bedtools --version"))) (substitute* '("scripts/perl/correlateMatrices.pl" "scripts/perl/matrix2scaling.pl" "scripts/perl/matrix2distance.pl" "scripts/perl/coverageCorrect.pl" "scripts/perl/matrix2anchorPlot.pl" "scripts/python/matrix2EigenVectors.py" "scripts/python/matrix2insulation-lite.py" "scripts/perl/matrix2compartment.pl" "scripts/perl/anchorPurge.pl" "scripts/perl/applyCorrection.pl" "scripts/perl/compareInsulation.pl" "scripts/perl/fillMissingData.pl" "scripts/perl/matrix2loess.pl" "scripts/python/getEigenVectors.py" "scripts/perl/aggregateBED.pl" "scripts/perl/collapseMatrix.pl" "scripts/perl/matrix2direction.pl" "scripts/perl/singletonRemoval.pl" "lib/cworld/dekker.pm" "scripts/perl/matrix2insulation.pl") (("(`|\")Rscript" _ pre) (string-append pre r "/bin/Rscript")))))) (add-after 'install 'install-scripts (lambda _ (let ((share (string-append #$output "/share/cworld-dekker"))) (mkdir-p share) (copy-recursively "scripts" share) ;; Make all scripts executable and wrap them. (let ((r (find-files share "\\.R$")) (py (find-files share "\\.py$")) (pl (find-files share "\\.pl$")) (wrap (lambda* (script var #:optional (extra "")) (let ((path (string-append (getenv var) extra))) (wrap-program script `(,var ":" prefix (,path))))))) (for-each (cut chmod <> #o555) (append r py pl)) (for-each (cut wrap <> "PERL5LIB" (string-append ":" #$output "/lib/perl5/site_perl")) pl) (for-each (cut wrap <> "GUIX_PYTHONPATH") py)))))))) (inputs (list gd perl-gd bedtools python-wrapper python-scipy python-numpy python-matplotlib python-h5py python-scikit-learn r-minimal)) (native-inputs (list perl-module-build)) (home-page "https://github.com/dekkerlab/cworld-dekker") (synopsis "Utility and analysis scripts for 3C, 4C, 5C, and Hi-C data") (description "This package is a collection of Perl, Python, and R scripts for manipulating 3C/4C/5C/Hi-C data.") (license license:asl2.0))) (define-public ensembl-vep (let* ((api-version "112") (api-module (lambda (name hash) (origin (method git-fetch) (uri (git-reference (url (string-append "https://github.com/Ensembl/" name ".git")) (commit (string-append "release/" api-version)))) (file-name (string-append name "-" api-version "-checkout")) (sha256 (base32 hash)))))) (package (name "ensembl-vep") (version api-version) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/Ensembl/ensembl-vep.git") (commit (string-append "release/" version)))) (file-name (git-file-name name version)) (sha256 (base32 "0nznmiln2q6bzd3xp8d5cw56higa5w3g9rmg66956bkfky53chvw")))) (build-system gnu-build-system) (arguments `(#:modules ((guix build gnu-build-system) (guix build utils) (ice-9 match)) #:phases (modify-phases %standard-phases (delete 'configure) (delete 'build) ;; Tests need to run after installation (delete 'check) (replace 'install (lambda* (#:key inputs outputs #:allow-other-keys) (let* ((modules '(("ensembl" "/") ("ensembl-variation" "/Variation") ("ensembl-funcgen" "/Funcgen") ("ensembl-io" "/"))) (scripts '(("convert_cache.pl" "vep_convert_cache.pl") ("INSTALL.pl" "vep_install.pl") ("haplo" #f) ("variant_recoder" #f) ("filter_vep" #f) ("vep" #f))) (out (assoc-ref outputs "out")) (bin (string-append out "/bin")) (perl (string-append out "/lib/perl5/site_perl"))) (for-each (match-lambda ((name path) (let ((dir (string-append perl "/Bio/EnsEMBL" path))) (mkdir-p dir) (copy-recursively (string-append (assoc-ref inputs (string-append "api-module-" name)) "/modules/Bio/EnsEMBL" path) dir)))) modules) (copy-recursively "modules/" perl) (mkdir-p bin) (for-each (match-lambda ((script new-name) (let ((location (string-append bin "/" (or new-name (basename script))))) (copy-file script location) (chmod location #o555) (wrap-program location `("PERL5LIB" ":" prefix (,(getenv "PERL5LIB") ,perl)))))) scripts) ;; Fix path to tools (with-directory-excursion (string-append perl "/Bio/EnsEMBL") (substitute* '("Funcgen/RunnableDB/ProbeMapping/PrePipelineChecks.pm" "VEP/BaseRunner.pm" "VEP/Utils.pm" "VEP/AnnotationSource/Cache/VariationTabix.pm" "VEP/AnnotationSource/Cache/BaseSerialized.pm" "Variation/Utils/BaseVepTabixPlugin.pm" "Variation/Utils/VEP.pm" "Variation/Pipeline/ReleaseDataDumps/PreRunChecks.pm") (("`which") (string-append "`" (assoc-ref inputs "which") "/bin/which"))))))) (add-after 'install 'check (lambda* (#:key tests? inputs outputs #:allow-other-keys) (when tests? (setenv "PERL5LIB" (string-append (getenv "PERL5LIB") ":" (assoc-ref outputs "out") "/lib/perl5/site_perl")) (copy-recursively (string-append (assoc-ref inputs "source") "/t") "/tmp/t") (for-each make-file-writable (find-files "/tmp/t")) ;; TODO: haplo needs Set/IntervalTree.pm (invoke "perl" "-e" (string-append " use Test::Harness; use Test::Exception; my $dirname = \"/tmp\"; opendir TEST, \"$dirname\\/t\"; my @test_files = map {\"$dirname\\/t\\/\".$_} grep {!/^\\./ && /\\.t$/} readdir TEST; closedir TEST; @test_files = grep {!/Haplo/} @test_files; runtests(@test_files); ")))))))) (inputs (list bioperl-minimal perl-bio-db-hts perl-dbi perl-dbd-mysql perl-libwww perl-list-moreutils perl-http-tiny perl-json which)) (propagated-inputs (list kentutils)) (native-inputs `(("unzip" ,unzip) ("perl" ,perl) ("api-module-ensembl" ,(api-module "ensembl" "10r576iqrz1p61mqbbfs87w4w3nldi45p51z52mq76f3n00l010h")) ("api-module-ensembl-variation" ,(api-module "ensembl-variation" "0ad03xnyyqpya1bkg6igq9abqxdmi58j89wn2kb3m4bvy1zs03mf")) ("api-module-ensembl-funcgen" ,(api-module "ensembl-funcgen" "1m3dxnr6k9x5hmcsxckpxlqx7vbc82lk74r84vcjijgxjkfa5rpp")) ("api-module-ensembl-io" ,(api-module "ensembl-io" "1xr6kdqqzmbi3m4bls589d1dfjvbs13dxlbf1y172xjyipvmag43")) ("perl-test-deep" ,perl-test-deep) ("perl-test-exception" ,perl-test-exception) ("perl-test-harness" ,perl-test-harness) ("perl-test-warnings" ,perl-test-warnings))) (home-page "http://www.ensembl.org/vep") (synopsis "Predict functional effects of genomic variants") (description "This package provides a Variant Effect Predictor, which predicts the functional effects of genomic variants. It also provides Haplosaurus, which uses phased genotype data to predict whole-transcript haplotype sequences, and Variant Recoder, which translates between different variant encodings.") (license license:asl2.0)))) (define-public r-signac (let ((commit "8ecdde291676102bb3b503f48926c993354b5471") (revision "1")) (package (name "r-signac") (version (git-version "1.12.0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/timoast/signac/") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0idkcqb1i13m164nxbdwgs3vflw0cxzm2ir84aw0i811vx9lqz8c")))) (properties `((upstream-name . "Signac"))) (build-system r-build-system) (inputs (list zlib)) (propagated-inputs (list r-biocgenerics r-data-table r-dplyr r-fastmatch r-future r-future-apply r-genomeinfodb r-genomicranges r-ggplot2 r-iranges r-irlba r-matrix r-patchwork r-pbapply r-rcpp r-rcpproll r-rsamtools r-s4vectors r-scales r-seuratobject r-stringi r-tidyr r-tidyselect r-vctrs)) (home-page "https://github.com/timoast/signac/") (synopsis "Analysis of single-cell chromatin data") (description "This package provides a framework for the analysis and exploration of single-cell chromatin data. The Signac package contains functions for quantifying single-cell chromatin data, computing per-cell quality control metrics, dimension reduction and normalization, visualization, and DNA sequence motif analysis.") (license license:expat)))) (define-public tombo (package (name "tombo") (version "1.5.1") (source (origin (method url-fetch) (uri (pypi-uri "ont-tombo" version)) (sha256 (base32 "1023hadgcsgi53kz53ql45207hfizf9sw57z0qij3ay1bx68zbpm")))) (build-system python-build-system) (arguments '(#:tests? #false)) ;no tests (native-inputs (list python-cython python-nose2)) ;; The package mainly consists of a command-line tool, but also has a ;; Python-API. Thus these must be propagated. (propagated-inputs (list python-future python-h5py python-mappy python-numpy python-scipy python-tqdm python-rpy2)) (home-page "https://github.com/nanoporetech/tombo") (synopsis "Analysis of raw nanopore sequencing data") (description "Tombo is a suite of tools primarily for the identification of modified nucleotides from nanopore sequencing data. Tombo also provides tools for the analysis and visualization of raw nanopore signal.") ;; Some parts may be BSD-3-licensed. (license license:mpl2.0))) (define-public python-pyvcf (let ((commit "476169cd457ba0caa6b998b301a4d91e975251d9") (revision "0")) (package (name "python-pyvcf") (version (git-version "0.6.8" revision commit)) ;; Use git, because the PyPI tarballs lack test data. (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/jamescasbon/PyVCF.git") ;; Latest release is not tagged. (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0qf9lwj7r2hjjp4bd4vc7nayrhblfm4qcqs4dbd43a6p4bj2jv5p")))) (build-system python-build-system) (arguments `(#:phases (modify-phases %standard-phases (add-after 'unpack 'patch-sample-script (lambda _ ;; Add Python 3 compatibility to this sample script. (substitute* "scripts/vcf_sample_filter.py" (("print (.*)\n" _ arg) (string-append "print(" arg ")\n"))))) (add-after 'install 'remove-installed-tests ;; Do not install test files. (lambda* (#:key inputs outputs #:allow-other-keys) (delete-file-recursively (string-append (site-packages inputs outputs) "/vcf/test"))))))) (native-inputs ;; Older setuptools is needed for use_2to3. (list python-cython python-setuptools-57)) (propagated-inputs (list python-pysam python-rpy2)) (home-page "https://github.com/jamescasbon/PyVCF") (synopsis "Variant Call Format parser for Python") (description "This package provides a @acronym{VCF,Variant Call Format} parser for Python.") (license license:expat)))) (define-public nanosv (package (name "nanosv") (version "1.2.4") (source (origin (method url-fetch) (uri (pypi-uri "NanoSV" version)) (sha256 (base32 "1wl2daj0bwrl8fx5xi8j8hfs3mp3vg3qycy66538n032v1qkc6xg")))) (build-system python-build-system) (inputs (list python-configparser python-pysam python-pyvcf)) (home-page "https://github.com/mroosmalen/nanosv") (synopsis "Structural variation detection tool for Oxford Nanopore data") (description "NanoSV is a software package that can be used to identify structural genomic variations in long-read sequencing data, such as data produced by Oxford Nanopore Technologies’ MinION, GridION or PromethION instruments, or Pacific Biosciences RSII or Sequel sequencers.") (license license:expat))) (define-public python-strawc (package (name "python-strawc") (version "0.0.2.1") (source (origin (method url-fetch) (uri (pypi-uri "strawC" version)) (sha256 (base32 "1z1gy8n56lhriy6hdkh9r82ndikndipq2cy2wh8q185qig4rimr6")))) (build-system python-build-system) (inputs (list curl zlib)) (propagated-inputs (list pybind11)) (home-page "https://github.com/aidenlab/straw") (synopsis "Stream data from .hic files") (description "Straw is library which allows rapid streaming of contact data from @file{.hic} files. This package provides Python bindings.") (license license:expat))) (define-public python-pybbi (package (name "python-pybbi") (version "0.3.0") (source (origin (method url-fetch) (uri (pypi-uri "pybbi" version)) (sha256 (base32 "1hvy2f28i2b41l1pq15vciqbj538n0lichp8yr6413jmgg06xdsk")))) (build-system python-build-system) (arguments `(#:tests? #false ; tests require network access #:phases (modify-phases %standard-phases (add-after 'unpack 'set-cc (lambda _ (setenv "CC" "gcc"))) (replace 'check (lambda* (#:key inputs outputs tests? #:allow-other-keys) (when tests? (add-installed-pythonpath inputs outputs) (copy-recursively "tests" "/tmp/tests") (with-directory-excursion "/tmp/tests" (invoke "python" "-m" "pytest" "-v")))))))) (native-inputs (list pkg-config python-pkgconfig python-pytest)) (inputs (list libpng openssl zlib)) (propagated-inputs (list python-cython python-numpy python-pandas python-six)) (home-page "https://github.com/nvictus/pybbi") (synopsis "Python bindings to UCSC Big Binary file library") (description "This package provides Python bindings to the UCSC Big Binary (bigWig/bigBed) file library. This provides read-level access to local and remote bigWig and bigBed files but no write capabilitites. The main feature is fast retrieval of range queries into numpy arrays.") (license license:expat))) (define-public python-dna-features-viewer (package (name "python-dna-features-viewer") (version "3.1.1") (source (origin (method url-fetch) (uri (pypi-uri "dna_features_viewer" version)) (sha256 (base32 "10a5pmh73spdgfml88zjqg1rn2j2zdxn06ir8a5q3arspyqvyqcb")))) (build-system pyproject-build-system) (arguments (list #:tests? #false ;there are none #:phases '(modify-phases %standard-phases ;; See https://github.com/Edinburgh-Genome-Foundry/DnaFeaturesViewer/issues/73 ;; and https://github.com/Edinburgh-Genome-Foundry/DnaFeaturesViewer/pull/74 (add-after 'unpack 'fix-biopython-compatibility (lambda _ (substitute* "dna_features_viewer/biotools.py" (("zip\$aa1 \\+ \"\\*\", aa3 \\+ \\[\"\\*\"\\]\$") "zip(aa1 + ('*',), aa3 + ('*',))"))))))) (propagated-inputs (list python-biopython python-matplotlib python-packaging)) (home-page "https://github.com/Edinburgh-Genome-Foundry/DnaFeaturesViewer") (synopsis "Plot features from DNA sequences") (description "DNA Features Viewer is a Python library to visualize DNA features, e.g. from GenBank or Gff files, or Biopython SeqRecords.") (license license:expat))) (define-public python-coolbox (package (name "python-coolbox") (version "0.3.8") (source (origin (method url-fetch) (uri (pypi-uri "coolbox" version)) (sha256 (base32 "0gqp76285w9klswr47y6kxbzwhv033b26jfa179kccfhiaq5p2xa")))) (build-system python-build-system) (arguments '(#:tests? #false)) ; there are none (inputs (list pybind11)) (propagated-inputs (list python-cooler python-dna-features-viewer python-fire python-h5py python-intervaltree python-ipywidgets jupyter python-matplotlib python-nbformat python-numpy python-numpydoc python-pandas python-pybbi python-pytest python-scipy python-statsmodels python-strawc python-svgutils python-termcolor python-voila)) (home-page "https://github.com/GangCaoLab/CoolBox") (synopsis "Genomic data visualization toolkit") (description "CoolBox is a toolkit for visual analysis of genomics data. It aims to be highly compatible with the Python ecosystem, easy to use and highly customizable with a well-designed user interface. It can be used in various visualization situations, for example, to produce high-quality genome track plots or fetch common used genomic data files with a Python script or command line, interactively explore genomic data within Jupyter environment or web browser.") (license license:gpl3+))) (define-public python-pyspoa (package (name "python-pyspoa") (version "0.0.5") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/nanoporetech/pyspoa") (commit (string-append "v" version)) (recursive? #true))) (file-name (git-file-name name version)) (sha256 (base32 "1lgf2shzhxkcsircd6vy46h27pjljd5q95fyz1cm3lkk702qbnzx")))) (build-system python-build-system) (arguments `(#:phases (modify-phases %standard-phases (add-before 'build 'build-libspoa (lambda _ (mkdir-p "src/build") (with-directory-excursion "src/build" (invoke "cmake" "-Dspoa_optimize_for_portability=ON" "-DCMAKE_BUILD_TYPE=Release" "-DCMAKE_CXX_FLAGS=\"-I ../vendor/cereal/include/\" -fPIC" "..") (invoke "make")))) (replace 'check (lambda* (#:key inputs outputs tests? #:allow-other-keys) (when tests? (add-installed-pythonpath inputs outputs) (invoke "python" "tests/test_pyspoa.py"))))))) (propagated-inputs (list pybind11)) (native-inputs `(("cmake" ,cmake-minimal))) (home-page "https://github.com/nanoporetech/pyspoa") (synopsis "Python bindings for the SIMD partial order alignment library") (description "This package provides Python bindings for spoa, a C++ implementation of the @dfn{partial order alignment} (POA) algorithm (as described in 10.1093/bioinformatics/18.3.452) which is used to generate consensus sequences") (license license:expat))) (define-public python-bwapy (package (name "python-bwapy") (version "0.1.4") (source (origin (method url-fetch) (uri (pypi-uri "bwapy" version)) (sha256 (base32 "090qwx3vl729zn3a7sksbviyg04kc71gpbm3nd8dalqp673x1npw")) (modules '((guix build utils))) (snippet '(for-each delete-file (find-files "." "\\.o$"))))) (build-system python-build-system) (arguments `(#:phases (modify-phases %standard-phases (add-after 'unpack 'relax-requirements (lambda _ (substitute* "setup.py" (("wheel>=0.34") "wheel>=0.30")))) ;; TODO: it's possible that the import error points to a real ;; problem with the C sources. (delete 'sanity-check)))) (propagated-inputs (list python-cffi python-setuptools python-wheel)) (inputs (list zlib)) (home-page "https://github.com/ACEnglish/bwapy") (synopsis "Python bindings to bwa aligner") (description "This package provides Python bindings to the bwa mem aligner.") ;; These Python bindings are licensed under Mozilla Public License 2.0, ;; bwa itself is licenced under GNU General Public License v3.0. (license license:mpl2.0))) (define-public scvelo (package (name "scvelo") (version "0.2.4") (source (origin (method url-fetch) (uri (pypi-uri "scvelo" version)) (sha256 (base32 "0h5ha1459ljs0qgpnlfsw592i8dxqn6p9bl08l1ikpwk36baxb7z")))) (build-system pyproject-build-system) (arguments (list #:test-flags ;; XXX: these two tests fail for unknown reasons '(list "-k" "not test_perfect_fit and not test_perfect_fit_2d") #:phases #~(modify-phases %standard-phases (add-after 'unpack 'matplotlib-compatibility (lambda _ (substitute* "scvelo/settings.py" (("warnings.filterwarnings\$\"ignore\", category=cbook.mplDeprecation\$") "")))) ;; Numba needs a writable dir to cache functions. (add-before 'check 'set-numba-cache-dir (lambda _ (setenv "NUMBA_CACHE_DIR" "/tmp"))) (replace 'check (lambda* (#:key tests? test-flags #:allow-other-keys) (when tests? ;; The discovered test file names must match the names of the ;; compiled files, so we cannot run the tests from ;; /tmp/guix-build-*. (with-directory-excursion (string-append #$output "/lib/python3.10/site-packages/scvelo/core/tests/") (apply invoke "pytest" "-v" test-flags)))))))) (propagated-inputs (list python-anndata python-hnswlib python-isort python-igraph python-loompy python-louvain python-matplotlib python-numba python-numpy python-pandas python-scanpy python-scikit-learn python-scipy python-umap-learn pybind11)) (native-inputs (list python-black python-flake8 python-hypothesis python-pytest python-setuptools-scm python-wheel)) (home-page "https://scvelo.org") (synopsis "RNA velocity generalized through dynamical modeling") (description "ScVelo is a scalable toolkit for RNA velocity analysis in single cells. RNA velocity enables the recovery of directed dynamic information by leveraging splicing kinetics. scVelo generalizes the concept of RNA velocity by relaxing previously made assumptions with a stochastic and a dynamical model that solves the full transcriptional dynamics. It thereby adapts RNA velocity to widely varying specifications such as non-stationary populations.") (license license:bsd-3))) (define-public scregseg (package (name "scregseg") (version "0.1.3") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/BIMSBbioinfo/scregseg") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "07g2barywa1wi8mggbxkbxqjw1fzd0a0l9cjdbkx4s40imb1dbxb")) (snippet '(delete-file "src/scregseg/_utils.c")))) (build-system pyproject-build-system) (arguments (list #:phases '(modify-phases %standard-phases ;; Numba needs a writable dir to cache functions. (add-before 'check 'set-numba-cache-dir (lambda _ (setenv "NUMBA_CACHE_DIR" "/tmp"))) ;; Cython extensions have to be built before running the tests. (add-before 'check 'build-extensions (lambda _ (invoke "python" "setup.py" "build_ext" "--inplace"))) (add-after 'unpack 'do-not-fail-to-find-sklearn (lambda _ ;; XXX: I have no idea why it cannot seem to find sklearn. (substitute* "setup.py" (("'sklearn',") ""))))))) (native-inputs (list python-cython)) (propagated-inputs (list python-scikit-learn python-scipy python-numpy python-hmmlearn python-pandas python-numba python-anndata python-scanpy python-pybedtools python-pysam python-matplotlib python-seaborn python-coolbox)) (home-page "https://github.com/BIMSBbioinfo/scregseg") (synopsis "Single-cell regulatory landscape segmentation") (description "Scregseg (Single-Cell REGulatory landscape SEGmentation) is a tool that facilitates the analysis of single cell ATAC-seq data by an HMM-based segmentation algorithm. Scregseg uses an HMM with Dirichlet-Multinomial emission probabilities to segment the genome either according to distinct relative cross-cell accessibility profiles or (after collapsing the single-cell tracks to pseudo-bulk tracks) to capture distinct cross-cluster accessibility profiles.") (license license:gpl3+))) (define-public megadepth (package (name "megadepth") (version "1.1.1") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/ChristopherWilks/megadepth") (commit version))) (file-name (git-file-name name version)) (sha256 (base32 "0hj69d2dgmk2zwgazik7xzc04fxxlk93p888kpgc52fmhd95qph7")))) (build-system cmake-build-system) (arguments `(#:tests? #false ; some tests seem to require connection to ; www.ebi.ac.uk; this may be caused by htslib. #:phases (modify-phases %standard-phases (add-after 'unpack 'prepare-CMakeLists.txt (lambda _ (rename-file "CMakeLists.txt.ci" "CMakeLists.txt") (substitute* "CMakeLists.txt" (("`cat ../VERSION`") ,version) (("target_link_libraries\\(megadepth_static") "#") (("target_link_libraries\\(megadepth_statlib") "#") (("add_executable\\(megadepth_static") "#") (("add_executable\\(megadepth_statlib") "#")) (substitute* "tests/test.sh" ;; Disable remote test (("./megadepth http://stingray.cs.jhu.edu/data/temp/test.bam") "#") ;; Prior to installation the binary's name differs from what ;; the test script assumes. (("./megadepth") "../build/megadepth_dynamic")))) (replace 'check (lambda* (#:key tests? #:allow-other-keys) (when tests? (with-directory-excursion "../source" (invoke "bash" "tests/test.sh" "use-local-test-data"))))) (replace 'install (lambda* (#:key outputs #:allow-other-keys) (let ((bin (string-append (assoc-ref outputs "out") "/bin"))) (mkdir-p bin) (copy-file "megadepth_dynamic" (string-append bin "/megadepth")))))))) (native-inputs (list diffutils perl grep)) (inputs (list curl htslib libdeflate libbigwig zlib)) (home-page "https://github.com/ChristopherWilks/megadepth") (synopsis "BigWig and BAM/CRAM related utilities") (description "Megadepth is an efficient tool for extracting coverage related information from RNA and DNA-seq BAM and BigWig files. It supports reading whole-genome coverage from BAM files and writing either indexed TSV or BigWig files, as well as efficient region coverage summary over intervals from both types of files.") (license license:expat))) (define-public megahit (package (name "megahit") (version "1.2.9") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/voutcn/megahit.git") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "1r5d9nkdmgjsbrpj43q9hy3s8jwsabaz3ji561v18hy47v58923c")))) (build-system cmake-build-system) (arguments (list #:test-target "simple_test" #:phases '(modify-phases %standard-phases (add-after 'unpack 'fix-tests (lambda _ (substitute* "src/megahit" (("os.path.join\$script_path, '..'\$") "os.path.join(script_path, '../source')"))))))) (inputs (list python-wrapper zlib)) (home-page "https://www.ncbi.nlm.nih.gov/pubmed/25609793") (synopsis "Meta-genome assembler") (description "Megahit is a fast and memory-efficient NGS assembler. It is optimized for metagenomes, but also works well on generic single genome assembly (small or mammalian size) and single-cell assembly.") (license license:gpl3))) (define-public mudskipper (package (name "mudskipper") (version "0.1.0") (source (origin (method url-fetch) (uri (crate-uri "mudskipper" version)) (file-name (string-append name "-" version ".tar.gz")) (sha256 (base32 "1y7fnlz6irmxdmv6bxzm95w4ws4vzldlrh8npvgxmdnrz9pgb1dv")))) (build-system cargo-build-system) (arguments `(#:tests? #false ;fail because the "mudskipper" crate cannot be found #:cargo-inputs (("rust-bio" ,rust-bio-0.39) ("rust-bio-types" ,rust-bio-types-0.12) ("rust-clap" ,rust-clap-2) ("rust-coitrees" ,rust-coitrees-0.2) ("rust-env-logger" ,rust-env-logger-0.9) ("rust-fnv" ,rust-fnv-1) ("rust-indicatif" ,rust-indicatif-0.16) ("rust-libradicl" ,rust-libradicl-0.4) ("rust-linecount" ,rust-linecount-0.1) ("rust-log" ,rust-log-0.4) ("rust-num-cpus" ,rust-num-cpus-1) ("rust-rust-htslib" ,rust-rust-htslib-0.38)))) (native-inputs (list cmake pkg-config)) (inputs (list zlib xz)) (home-page "https://github.com/OceanGenomics/mudskipper") (synopsis "Convert genomic alignments to transcriptomic BAM/RAD files") (description "Mudskipper is a tool for projecting genomic alignments to transcriptomic coordinates.") (license license:bsd-3))) (define-public r-ascat (package (name "r-ascat") (version "2.5.2") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/Crick-CancerGenomics/ascat.git") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "0cc0y3as6cb64iwnx0pgbajiig7m4z723mns9d5i4j09ccid3ccm")))) (build-system r-build-system) (arguments `(#:phases (modify-phases %standard-phases (add-after 'unpack 'move-to-ascat-dir (lambda _ (chdir "ASCAT")))))) (propagated-inputs (list r-rcolorbrewer)) (home-page "https://github.com/VanLoo-lab/ascat/") (synopsis "Allele-Specific Copy Number Analysis of Tumors in R") (description "This package provides the @acronym{ASCAT,Allele-Specific Copy Number Analysis of Tumors} R package that can be used to infer tumour purity, ploidy and allele-specific copy number profiles.") (license license:gpl3))) (define-public r-battenberg (package (name "r-battenberg") (version "2.2.9") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/Wedge-lab/battenberg.git") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "0nmcq4c7y5g8h8lxsq9vadz9bj4qgqn118alip520ny6czaxki4h")))) (build-system r-build-system) (propagated-inputs (list r-devtools r-readr r-doparallel r-ggplot2 r-rcolorbrewer r-gridextra r-gtools r-ascat)) (home-page "https://github.com/Wedge-lab/battenberg") (synopsis "Subclonal copy number estimation in R") (description "This package contains the Battenberg R package for subclonal copy number estimation, as described by @url{doi:10.1016/j.cell.2012.04.023,Nik-Zainal et al.}") (license license:gpl3))) (define-public r-catch (let ((commit "196ddd5a51b1a5f5daa01de53fdaad9b7505e084") (revision "1")) (package (name "r-catch") (version (git-version "1.0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/zhanyinx/CaTCH") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "11c7f1fc8f57wnwk1hrgr5y814m80zj8gkz5021vxyxy2v02cqgd")))) (build-system r-build-system) (arguments `(#:phases (modify-phases %standard-phases (add-after 'unpack 'chdir (lambda _ (chdir "CaTCH")))))) (home-page "https://github.com/zhanyinx/CaTCH_R") (synopsis "Call a hierarchy of domains based on Hi-C data") (description "This package allows building the hierarchy of domains starting from Hi-C data. Each hierarchical level is identified by a minimum value of physical insulation between neighboring domains.") (license license:gpl2+)))) (define-public r-spectre (let ((commit "f6648ab3eb9499300d86502b5d60ec370ae9b61a") (revision "1")) (package (name "r-spectre") (version (git-version "0.5.5" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/ImmuneDynamics/Spectre") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0g38grrhbqqa4bmcilvdyawbkcnax6k4vffx2giywp18mbirmj0x")))) (properties `((upstream-name . "Spectre"))) (build-system r-build-system) (propagated-inputs (list r-biobase r-biocmanager r-caret r-class r-colorramps r-data-table r-devtools r-dplyr r-exactextractr r-factoextra r-flowcore r-flowsom r-flowviz r-fnn r-ggplot2 r-ggpointdensity r-ggpubr r-ggraph r-ggthemes r-gridextra r-gridextra r-gtools r-hdf5array r-irlba r-pheatmap r-plyr r-qs r-raster r-rcolorbrewer r-rgeos r-rhdf5 r-rstudioapi r-rsvd r-rtsne r-s2 r-scales r-sf r-sp r-stars r-stringr r-tidygraph r-tidyr r-tidyr r-tiff r-umap)) (home-page "https://github.com/ImmuneDynamics/Spectre") (synopsis "High-dimensional cytometry and imaging analysis") (description "This package provides a computational toolkit in R for the integration, exploration, and analysis of high-dimensional single-cell cytometry and imaging data.") (license license:expat)))) (define-public r-compgenomrdata (let ((commit "24484cb77631e1123ead6c329b9d62c160e600c6") (revision "1")) (package (name "r-compgenomrdata") (version (git-version "0.1.0" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/compgenomr/compGenomRData") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "06gdvz4m4qlb1ylv10qfx09zv4c95cm7nps4y2s67m946kv8czv8")))) (properties `((upstream-name . "compGenomRData"))) (build-system r-build-system) (home-page "https://github.com/compgenomr/compGenomRData") (synopsis "Data for Computational Genomics with R book") (description "This package provides data for the book \"Computational Genomics with R\".") (license license:gpl3)))) (define-public r-cytonorm (let ((commit "166f9ff3d692278241018c2846cb4f86ab16065b") (revision "1")) (package (name "r-cytonorm") (version (git-version "0.0.10" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/saeyslab/CytoNorm") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "0vbqy3b26j1zqmwgqx59kkn9pm2m0qwlcppskvahrxcwrj6m1s5y")))) (properties `((upstream-name . "CytoNorm"))) (build-system r-build-system) (propagated-inputs (list r-cytoml r-dplyr r-emdist r-flowcore r-flowsom r-flowworkspace r-ggplot2 r-gridextra r-pheatmap r-stringr)) (home-page "https://github.com/saeyslab/CytoNorm") (synopsis "Normalize cytometry data measured across multiple batches") (description "This package can be used to normalize cytometry samples when a control sample is taken along in each of the batches. This is done by first identifying multiple clusters/cell types, learning the batch effects from the control samples and applying quantile normalization on all markers of interest.") (license license:gpl2+)))) (define-public r-kbet (let ((commit "f35171dfb04c7951b8a09ac778faf7424c4b6bc0") (revision "1")) (package (name "r-kbet") (version (git-version "0.99.6" revision commit)) (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/theislab/kBET") (commit commit))) (file-name (git-file-name name version)) (sha256 (base32 "1r91prl2kki3zk694vhlmxdlqh0ixlhs8jfcqw6wc7cdsa0nv67k")))) (properties `((upstream-name . "kBET"))) (build-system r-build-system) (propagated-inputs (list r-cluster r-fnn r-ggplot2 r-mass r-rcolorbrewer)) (native-inputs (list r-knitr)) (home-page "https://github.com/theislab/kBET") (synopsis "k-nearest neighbour batch effect test") (description "This tool detects batch effects in high-dimensional data based on chi^2-test.") ;; Any version of the GPL (license license:gpl3+)))) (define-public python-vireosnp (package (name "python-vireosnp") (version "0.5.7") (source (origin (method url-fetch) (uri (pypi-uri "vireoSNP" version)) (sha256 (base32 "02ybhzivsxwnb1axlgbs63wni1j27xajnkl4jw1ps5vmsz2l4b0d")))) (build-system python-build-system) (propagated-inputs (list python-matplotlib python-numpy python-scipy)) (home-page "https://github.com/huangyh09/vireoSNP") (synopsis "Deconvolution based on SNP for multiplexed scRNA-seq data") (description "This package provides a deconvolution based on Single Nucleotide Position (SNP) for multiplexed scRNA-seq data. The name vireo stand for Variational Inference for Reconstructing Ensemble Origin by expressed SNPs in multiplexed scRNA-seq data and follows the clone identification from single-cell data named @url{https://github.com/PMBio/cardelino, cardelino}.") (license license:asl2.0))) (define-public ccwl (package (name "ccwl") (version "0.3.0") (source (origin (method url-fetch) (uri (string-append "https://ccwl.systemreboot.net/releases/ccwl-" version ".tar.lz")) (sha256 (base32 "0za710mcn9di1njli3dk3660n3836ip8b4msb8f958498va95y7j")))) (build-system gnu-build-system) (arguments `(#:make-flags '("GUILE_AUTO_COMPILE=0") ; to prevent guild warnings #:modules (((guix build guile-build-system) #:select (target-guile-effective-version)) ,@%default-gnu-modules) #:imported-modules ((guix build guile-build-system) ,@%default-gnu-imported-modules) #:phases (modify-phases %standard-phases (add-after 'patch-source-shebangs 'patch-more-source-shebangs (lambda* (#:key inputs #:allow-other-keys) (substitute* "scripts/ccwl" (("^exec guile") (string-append "exec " (search-input-file inputs "/bin/guile")))))) (add-after 'install 'wrap (lambda* (#:key inputs outputs #:allow-other-keys) (let ((out (assoc-ref outputs "out")) (effective-version (target-guile-effective-version))) (wrap-program (string-append out "/bin/ccwl") `("GUILE_LOAD_PATH" prefix (,(string-append out "/share/guile/site/" effective-version) ,(getenv "GUILE_LOAD_PATH"))) `("GUILE_LOAD_COMPILED_PATH" prefix (,(string-append out "/lib/guile/" effective-version "/site-ccache") ,(getenv "GUILE_LOAD_COMPILED_PATH")))))))))) (inputs (list bash-minimal guile-3.0 guile-libyaml)) (native-inputs (list pkg-config lzip ;; To build documentation cwltool graphviz skribilo)) (home-page "https://ccwl.systemreboot.net") (synopsis "Concise common workflow language") (description "The @acronym{ccwl, Concise Common Workflow Language} is a concise syntax to express CWL workflows. ccwl is a compiler to generate CWL workflows from concise descriptions in ccwl. It is implemented as an @acronym{EDSL, Embedded Domain Specific Language} in the Scheme programming language.") (license license:gpl3+))) (define-public hh-suite (package (name "hh-suite") (version "3.3.0") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/soedinglab/hh-suite") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "1bcmzg0ii6nkda2xm5jdddbwkgsag7k38j20af0c9chr2mbxwx4d")) (modules '((guix build utils))) (snippet '(delete-file-recursively "lib/simde")))) (build-system cmake-build-system) (arguments '(#:tests? #false)) ;no test target (inputs (list openmpi simde)) (native-inputs (list perl pkg-config xxd)) (home-page "https://bmcbioinformatics.biomedcentral.com/articles/10.1186/s12859-019-3019-7") (synopsis "Remote protein homology detection suite") (description "The HH-suite is a software package for sensitive protein sequence searching based on the pairwise alignment of hidden Markov models (HMMs).") (license license:gpl3+))) (define-public wfmash (package (name "wfmash") (version "0.12.5") (source (origin ;; There are no release tarballs after version 0.10.5. (method git-fetch) (uri (git-reference (url "https://github.com/waveygang/wfmash") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "1qh2chnwp7nqgp88afc4xzdkd21vh6cfqq73siqw7vc0qinqadm6")) (snippet #~(begin (use-modules (guix build utils)) ;; Unbundle atomic-queue. (delete-file-recursively "src/common/atomic_queue") (substitute* "src/align/include/computeAlignments.hpp" (("\"common/atomic_queue/atomic_queue.h\"") "<atomic_queue/atomic_queue.h>")) ;; Remove compiler optimizations. (substitute* (find-files "." "CMakeLists\\.txt") (("-march=native ") "")))))) (build-system cmake-build-system) (arguments (list #:configure-flags #~(list "-DWFA_PNG_AND_TSV=ON") #:phases #~(modify-phases %standard-phases (replace 'check ;; Adapted from .github/workflows/test_on_push.yml (lambda* (#:key tests? inputs #:allow-other-keys) (when tests? (let ((samtools (search-input-file inputs "/bin/samtools"))) ;; This is the easiest way to access the data ;; needed for the test suite. (symlink "../source/data" "data") (and ;; This test takes 60 minutes on riscv64-linux. #$@(if (not (target-riscv64?)) #~((begin ;; Test with a subset of the LPA dataset (PAF output) (setenv "ASAN_OPTIONS" "detect_leaks=1:symbolize=1") (setenv "LSAN_OPTIONS" "verbosity=0:log_threads=1") (with-output-to-file "LPA.subset.paf" (lambda _ (invoke "bin/wfmash" "data/LPA.subset.fa.gz" "data/LPA.subset.fa.gz" "-X" "-n" "10" "-T" "wflign_info." "-u" "./"))) (invoke "head" "LPA.subset.paf"))) #~()) ;; This test takes about 5 hours on riscv64-linux. #$@(if (not (target-riscv64?)) #~((begin ;; Test with a subset of the LPA dataset (SAM output) (setenv "ASAN_OPTIONS" "detect_leaks=1:symbolize=1") (setenv "LSAN_OPTIONS" "verbosity=0:log_threads=1") (with-output-to-file "LPA.subset.sam" (lambda _ (invoke "bin/wfmash" "data/LPA.subset.fa.gz" "data/LPA.subset.fa.gz" "-X" "-N" "-a" "-T" "wflign_info."))) (with-output-to-file "LPA.subset.sam-view" (lambda _ (invoke samtools "view" "LPA.subset.sam" "-bS"))) (with-output-to-file "LPA.subset.bam" (lambda _ (invoke samtools "sort" "LPA.subset.sam-view"))) (invoke samtools "index" "LPA.subset.bam") ;; samtools view LPA.subset.bam | head | cut -f 1-9 ;(invoke samtools "view" "LPA.subset.bam") ;; There should be an easier way to do this with pipes. (with-output-to-file "LPA.subset.bam-incr1" (lambda _ (invoke samtools "view" "LPA.subset.bam"))) (with-output-to-file "LPA.subset.bam-incr2" (lambda _ (invoke "head" "LPA.subset.bam-incr1"))) (invoke "cut" "-f" "1-9" "LPA.subset.bam-incr2"))) #~()) ;; This test takes 60 minutes on riscv64-linux. #$@(if (not (target-riscv64?)) #~((begin ;; Test with a subset of the LPA dataset, ;; setting a lower identity threshold (PAF output) (setenv "ASAN_OPTIONS" "detect_leaks=1:symbolize=1") (setenv "LSAN_OPTIONS" "verbosity=0:log_threads=1") (with-output-to-file "LPA.subset.p90.paf" (lambda _ (invoke "bin/wfmash" "data/LPA.subset.fa.gz" "data/LPA.subset.fa.gz" "-X" "-p" "90" "-n" "10" "-T" "wflign_info."))) (invoke "head" "LPA.subset.p90.paf"))) #~()) (begin ;; Test aligning short reads (500 bps) to a reference (SAM output) (setenv "ASAN_OPTIONS" "detect_leaks=1:symbolize=1") (setenv "LSAN_OPTIONS" "verbosity=0:log_threads=1") (with-output-to-file "reads.500bps.sam" (lambda _ (invoke "bin/wfmash" "data/reference.fa.gz" "data/reads.500bps.fa.gz" "-s" "0.5k" "-N" "-a"))) (with-output-to-file "reads.500bps.sam-view" (lambda _ (invoke samtools "view" "reads.500bps.sam" "-bS"))) (with-output-to-file "reads.500bps.bam" (lambda _ (invoke samtools "sort" "reads.500bps.sam-view"))) (invoke samtools "index" "reads.500bps.bam") (with-output-to-file "reads.500bps.bam-view" (lambda _ (invoke samtools "view" "reads.500bps.bam"))) (invoke "head" "reads.500bps.bam-view")) (begin ;; Test with few very short reads (255bps) (PAF output) (setenv "ASAN_OPTIONS" "detect_leaks=1:symbolize=1") (setenv "LSAN_OPTIONS" "verbosity=0:log_threads=1") (with-output-to-file "reads.255bps.paf" (lambda _ (invoke "bin/wfmash" "data/reads.255bps.fa.gz" "-w" "16" "-s" "100" "-L"))) (invoke "head" "reads.255bps.paf")))))))))) (inputs (list atomic-queue gsl htslib jemalloc zlib)) (native-inputs (list pkg-config samtools)) (synopsis "Base-accurate DNA sequence aligner") (description "@code{wfmash} is a DNA sequence read mapper based on mash distances and the wavefront alignment algorithm. It is a fork of MashMap that implements base-level alignment via the wflign tiled wavefront global alignment algorithm. It completes MashMap with a high-performance alignment module capable of computing base-level alignments for very large sequences.") (home-page "https://github.com/waveygang/wfmash") (license license:expat))) (define-public gdcm (package (name "gdcm") (version "3.0.20") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/malaterre/gdcm") (commit (string-append "v" version)) (recursive? #t))) (file-name (git-file-name name version)) (sha256 (base32 "1rf0p7dnakjry0fa6ax1h762bn0l5n6ibfdxn077mjvwgpqan51l")))) (build-system cmake-build-system) (outputs '("out" "doc")) (arguments (list #:phases #~(modify-phases %standard-phases (add-before 'build 'set-HOME ;; The build spams ‘Fontconfig error: No writable cache ;; directories’ in a seemingly endless loop otherwise. (lambda _ (setenv "HOME" "/tmp")))) #:configure-flags #~(list "-DGDCM_BUILD_TESTING=true" (string-append "-DCMAKE_CTEST_ARGUMENTS=-E;" "'TestFileMetaInformation" "|TestElement2" "|TestSCUValidation" "|TestWriter" "|TestAnonymizer4" "|TestPrinter1" "|TestEcho" ;; The scanner tests depend on TestWriter output "|TestStrictScanner1" "|TestStrictScanner2_1" "|TestStrictScanner2" "|TestStrictScanner2_2" "|TestFind'") "-DGDCM_DOCUMENTATION:BOOL=ON" "-DGDCM_PDF_DOCUMENTATION:BOOL=OFF" (string-append "-DGDCM_INSTALL_DOC_DIR=" #$output:doc "/share/doc/" #$name)))) (native-inputs (list docbook-xsl doxygen graphviz libxslt)) (home-page "https://gdcm.sourceforge.net/wiki/index.php/Main_Page") (synopsis "Grassroots DICOM library") (description "Grassroots DICOM (GDCM) is an implementation of the DICOM standard designed to be open source so that researchers may access clinical data directly. GDCM includes a file format definition and a network communications protocol, both of which should be extended to provide a full set of tools for a researcher or small medical imaging vendor to interface with an existing medical database.") (license license:bsd-3))) (define-public wiggletools (package (name "wiggletools") (version "1.2.11") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/Ensembl/WiggleTools/") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "1g3qla4l1g583nzlgyww5jqxpq87ndpn9cmjls098bgqjyn5292q")))) (build-system gnu-build-system) (arguments (list ;; Tests require internet access #:tests? #false #:make-flags #~(list "Wiggletools" (string-append "CC=" #$(cc-for-target))) #:phases #~(modify-phases %standard-phases (delete 'configure) (replace 'install (lambda _ (install-file "bin/wiggletools" (string-append #$output "/bin"))))))) (inputs (list curl ; XXX: needed by libbigwig htslib libbigwig gsl xz zlib)) (home-page "https://github.com/Ensembl/WiggleTools/") (synopsis "Operations on the space of numerical functions defined on the genome") (description "The WiggleTools package allows genomewide data files to be manipulated as numerical functions, equipped with all the standard functional analysis operators (sum, product, product by a scalar, comparators), and derived statistics (mean, median, variance, stddev, t-test, Wilcoxon's rank sum test, etc).") (license license:asl2.0))) (define-public flair (package (name "flair") (version "1.6.4") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/BrooksLabUCSC/flair") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "0jviacx6qx5rwgi3wvl7a8a8ml19r6cpngddivlk13f6g9072din")))) (build-system python-build-system) (arguments (list #:tests? #false ;there are none #:phases #~(modify-phases %standard-phases ;; TODO: implement as a feature of python-build-system (PEP-621, ;; PEP-631, PEP-660) (replace 'build (lambda _ (setenv "SETUPTOOLS_SCM_PRETEND_VERSION" #$version) ;; ZIP does not support timestamps before 1980. (setenv "SOURCE_DATE_EPOCH" "315532800") (invoke "python" "-m" "build" "--wheel" "--no-isolation" "."))) (replace 'install (lambda _ (apply invoke "pip" "--no-cache-dir" "--no-input" "install" "--no-deps" "--prefix" #$output (find-files "dist" "\\.whl$")))) (add-after 'install 'wrap-executable (lambda _ (for-each (lambda (script) (wrap-program script `("R_HOME" ":" = (,(string-append #$r-minimal "/lib/R"))) `("R_LIBS_SITE" ":" = (,(getenv "R_LIBS_SITE"))))) (find-files (string-append #$output "/bin")))))))) (propagated-inputs (list python-mappy python-numpy python-ncls python-pybedtools python-pysam python-rpy2 python-scipy python-tqdm)) ;; Used by rpy2 (inputs (list bash-minimal r-minimal ;for R_LIBS_SITE r-apeglm ;for runDE r-deseq2 ;for runDE r-drimseq ;for runDS r-ggplot2 ;runDS, runDU r-lazyeval ;for rpy2 r-qqman ;for runDE r-rlang)) ;for rpy2 (native-inputs (list python-pypa-build python-setuptools)) (home-page "https://flair.readthedocs.io/en/latest/") (synopsis "Full-length alternative isoform analysis of RNA") (description "This package implements FLAIR (Full-Length Alternative Isoform analysis of RNA) for the correction, isoform definition, and alternative splicing analysis of noisy reads. FLAIR has primarily been used for nanopore cDNA, native RNA, and PacBio sequencing reads.") (license license:bsd-3))) (define-public go-github-com-biogo-graph (package (name "go-github-com-biogo-graph") (version "0.0.0-20150317020928-057c1989faed") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/biogo/graph") (commit (go-version->git-ref version)))) (file-name (git-file-name name version)) (sha256 (base32 "1kpzs5dfd5dsk4mg1g2qjz1prqd84ixhrcxxnf90hq25vxcnk7lh")))) (build-system go-build-system) (arguments '(#:import-path "github.com/biogo/graph" #:tests? #false)) ;TODO: one of 13 tests fails for unknown reasons (propagated-inputs (list go-gopkg-in-check-v1)) (home-page "https://github.com/biogo/graph") (synopsis "Undirected graph analysis for biogo") (description "The package @code{graph} implements graph manipulation functions.") (license license:bsd-3))) (define-public go-github-com-biogo-store-interval (package (name "go-github-com-biogo-store-interval") (version "0.0.0-20201120204734-aad293a2328f") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/biogo/store") (commit (go-version->git-ref version)))) (file-name (git-file-name name version)) (sha256 (base32 "0skizrp1j6vgbl0g1kmh73picagqlvwckaqs0gkl6rai5lckxj8a")))) (build-system go-build-system) (arguments '(#:import-path "github.com/biogo/store/interval" #:unpack-path "github.com/biogo/store")) (propagated-inputs (list go-gopkg-in-check-v1 go-github-com-kr-pretty)) (home-page "https://github.com/biogo/store") (synopsis "Interval store type for biogo") (description "The @code{store} package provides a number of data store types that are useful for bioinformatic analysis.") (license license:bsd-3))) (define-public go-github-com-biogo-store-kdtree (package (inherit go-github-com-biogo-store-interval) (name "go-github-com-biogo-store-kdtree") (arguments '(#:import-path "github.com/biogo/store/kdtree" #:unpack-path "github.com/biogo/store")) (propagated-inputs (list go-gopkg-in-check-v1 go-github-com-kr-pretty)) (synopsis "kdtree store type for biogo"))) (define-public go-github-com-biogo-store-llrb (package (inherit go-github-com-biogo-store-interval) (name "go-github-com-biogo-store-llrb") (arguments '(#:import-path "github.com/biogo/store/llrb" #:unpack-path "github.com/biogo/store")) (propagated-inputs (list go-gopkg-in-check-v1 go-github-com-kr-pretty)) (synopsis "LLRB store for biogo"))) (define-public go-github-com-biogo-store-step (package (inherit go-github-com-biogo-store-interval) (name "go-github-com-biogo-store-step") (arguments '(#:import-path "github.com/biogo/store/step" #:unpack-path "github.com/biogo/store")) (propagated-inputs (list go-gopkg-in-check-v1 go-github-com-kr-pretty)) (synopsis "Step store for biogo"))) (define-public go-github-com-biogo-hts-bam (package (name "go-github-com-biogo-hts-bam") (version "1.4.4") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/biogo/hts") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "1vkcqxyajghx5p5j7g2i376nbsxh8q2smk0smlv8mi34yr7hlw5b")))) (build-system go-build-system) (arguments '(#:import-path "github.com/biogo/hts/bam" #:unpack-path "github.com/biogo/hts")) (propagated-inputs (list go-gopkg-in-check-v1)) (home-page "https://github.com/biogo/hts") (synopsis "HTS BAM module for biogo") (description "This package provides tools for handling BAM files.") (license license:bsd-3))) (define-public go-github-com-biogo-hts-sam (package (inherit go-github-com-biogo-hts-bam) (name "go-github-com-biogo-hts-sam") (arguments '(#:import-path "github.com/biogo/hts/sam" #:unpack-path "github.com/biogo/hts")) (propagated-inputs (list go-gopkg-in-check-v1)) (synopsis "HTS SAM module for biogo") (description "This package provides tools for handling SAM files."))) (define-public go-github-com-biogo-hts-tabix (package (inherit go-github-com-biogo-hts-bam) (name "go-github-com-biogo-hts-tabix") (arguments '(#:import-path "github.com/biogo/hts/tabix" #:unpack-path "github.com/biogo/hts")) (propagated-inputs (list go-gopkg-in-check-v1)) (synopsis "HTS Tabix module for biogo") (description "This package provides tools for handling Tabix files."))) (define-public go-github-com-biogo-hts-bgzf (package (inherit go-github-com-biogo-hts-bam) (name "go-github-com-biogo-hts-bgzf") (arguments '(#:import-path "github.com/biogo/hts/bgzf" #:unpack-path "github.com/biogo/hts")) (propagated-inputs (list go-gopkg-in-check-v1)) (synopsis "HTS bgzf module for biogo") (description "This package provides tools for handling bgzf files."))) (define-public go-github-com-biogo-hts-cram (package (inherit go-github-com-biogo-hts-bam) (name "go-github-com-biogo-hts-cram") (arguments '(#:import-path "github.com/biogo/hts/cram" #:unpack-path "github.com/biogo/hts" #:tests? #false)) ;require network access (propagated-inputs (list go-gopkg-in-check-v1 go-github-com-ulikunitz-xz go-github-com-kortschak-utter)) (synopsis "HTS CRAM module for biogo") (description "This package provides tools for handling CRAM files."))) (define-public go-github-com-biogo-hts-csi (package (inherit go-github-com-biogo-hts-bam) (name "go-github-com-biogo-hts-csi") (arguments '(#:import-path "github.com/biogo/hts/csi" #:unpack-path "github.com/biogo/hts")) (propagated-inputs (list go-gopkg-in-check-v1)) (synopsis "Coordinate sorted indexing for biogo") (description "This package implements CSIv1 and CSIv2 coordinate sorted indexing."))) (define-public go-github-com-biogo-hts-fai (package (inherit go-github-com-biogo-hts-bam) (name "go-github-com-biogo-hts-fai") (arguments '(#:import-path "github.com/biogo/hts/fai" #:unpack-path "github.com/biogo/hts")) (propagated-inputs (list go-gopkg-in-check-v1)) (synopsis "Fasta sequence file index handling for biogo") (description "This package implements FAI fasta sequence file index handling."))) (define-public go-github-com-biogo-biogo (package (name "go-github-com-biogo-biogo") (version "1.0.4") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/biogo/biogo") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "0ali1mqf3dc26myv6l7wmqfr8i25461rbq3qdad8s0wi29622199")))) (build-system go-build-system) (arguments '(#:import-path "github.com/biogo/biogo")) (propagated-inputs (list go-gopkg-in-check-v1 go-github-com-biogo-store-interval go-github-com-biogo-store-kdtree go-github-com-biogo-store-llrb go-github-com-biogo-store-step go-github-com-biogo-hts-bam go-github-com-biogo-graph)) (home-page "https://github.com/biogo/biogo") (synopsis "Bioinformatics library for Go") (description "Bíogo is a bioinformatics library for the Go language.") (license license:bsd-3))) (define-public python-gseapy (package (name "python-gseapy") (version "1.0.4") (source (origin (method git-fetch) (uri (git-reference (url "https://github.com/zqfang/GSEApy") (commit (string-append "v" version)))) (file-name (git-file-name name version)) (sha256 (base32 "06gh09dwwj2xr5zx8i41smy8arx2pw7rll7sk50np28z419bnyz9")))) (build-system cargo-build-system) (arguments (list #:install-source? #false #:features '(list "extension-module") #:cargo-test-flags '(list "--features=extension-module") #:cargo-inputs `(("rust-csv" ,rust-csv-1) ("rust-itertools" ,rust-itertools-0.10) ("rust-pyo3" ,rust-pyo3-0.16) ("rust-rand" ,rust-rand-0.8) ("rust-rayon" ,rust-rayon-1) ("rust-serde" ,rust-serde-1)) #:imported-modules (append %cargo-build-system-modules %pyproject-build-system-modules) #:modules '((guix build cargo-build-system) ((guix build pyproject-build-system) #:prefix py:) (guix build utils)) #:phases #~(modify-phases %standard-phases (add-after 'install 'prepare-python-module (lambda _ ;; We don't use maturin, nor do we use setuptools-rust. (delete-file "pyproject.toml") (call-with-output-file "pyproject.toml" (lambda (port) (format port "\ [build-system] build-backend = 'setuptools.build_meta' requires = ['setuptools'] "))) (delete-file "setup.py") (call-with-output-file "setup.cfg" (lambda (port) (format port "\ [metadata] name = gseapy version = ~a [options] packages = find: [options.packages.find] exclude = src docs tests Cargo.toml " #$version))))) ;; We delete the Cargo checks but run the Python tests later. ;; See https://github.com/zqfang/GSEApy/issues/207 (delete 'check) (add-after 'prepare-python-module 'enable-bytecode-determinism (assoc-ref py:%standard-phases 'enable-bytecode-determinism)) (add-after 'enable-bytecode-determinism 'build-python-module (assoc-ref py:%standard-phases 'build)) (add-after 'build-python-module 'install-python-module (assoc-ref py:%standard-phases 'install)) (add-after 'install-python-module 'install-python-library (lambda _ (let ((site (string-append #$output "/lib/python" #$(version-major+minor (package-version python)) "/site-packages"))) (mkdir-p site) (copy-file "target/release/libgse.so" (string-append site "/gseapy/gse.so"))))) (add-after 'install-python-library 'add-install-to-pythonpath (assoc-ref py:%standard-phases 'add-install-to-pythonpath)) (add-after 'add-install-to-pythonpath 'check (lambda* (#:key tests? #:allow-other-keys) (when tests? (invoke "pytest" "-vv" "tests" ;; These tests need access to the internet "-k" "not test_enrichr and not test_prerank"))))))) (inputs (list python-wrapper)) (native-inputs (list python-pytest)) (propagated-inputs (list python-numpy python-scipy python-pandas python-matplotlib python-requests)) (home-page "https://github.com/zqfang/gseapy") (synopsis "Gene Set Enrichment Analysis in Python") (description "GSEApy is a Python/Rust implementation for GSEA and wrapper for Enrichr. GSEApy can be used for RNA-seq, ChIP-seq, Microarray data. It can be used for convenient GO enrichment and to produce publication quality figures in Python.") (license license:bsd-3))) ;;; ;;; Avoid adding new packages to the end of this file. To reduce the chances ;;; of a merge conflict, place them above by existing packages with similar ;;; functionality or similar names. ;;;


context:
space:
mode: