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author | Andreas Enge <andreas@enge.fr> | 2025-03-28 10:52:48 +0100 |
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committer | Andreas Enge <andreas@enge.fr> | 2025-04-29 11:34:51 +0200 |
commit | 743123249648baaa911eb3aecccfb232ddf3e4d8 (patch) | |
tree | bae742d1b12a8c038c79d72aeb1d93cb159d398e | |
parent | b3a5bd2ce5f58d38e5488d7f600d983f4c7c6deb (diff) | |
download | guix-743123249648baaa911eb3aecccfb232ddf3e4d8.tar.gz guix-743123249648baaa911eb3aecccfb232ddf3e4d8.zip |
gnu: Remove variant-tools.
The package does not compile any more and has no dependent packages.
The last release dates from 2020; there is an additional commit in 2022;
the git repository has been archived in 2023.
* gnu/packages/bioinformatics.scm (variant-tools): Delete variable.
Change-Id: Idb5df024121c5085f764f179d31ac67cff3fc5c7
-rw-r--r-- | gnu/packages/bioinformatics.scm | 37 |
1 files changed, 0 insertions, 37 deletions
diff --git a/gnu/packages/bioinformatics.scm b/gnu/packages/bioinformatics.scm index 74cf9b0bf5..7523706358 100644 --- a/gnu/packages/bioinformatics.scm +++ b/gnu/packages/bioinformatics.scm @@ -15510,43 +15510,6 @@ 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")) |