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authorRicardo Wurmus <rekado@elephly.net>2022-01-11 14:47:36 +0100
committerRicardo Wurmus <rekado@elephly.net>2022-01-11 14:48:26 +0100
commit61a1c3f72df3b0333865d6071beaea60294f2ce7 (patch)
tree4eed30288db0f76378722a158afd5eb891c49676
parent81ab20162653cf215d3305086d207472eab6385c (diff)
downloadguix-61a1c3f72df3b0333865d6071beaea60294f2ce7.tar.gz
guix-61a1c3f72df3b0333865d6071beaea60294f2ce7.zip
gnu: Add r-transcriptr.
* gnu/packages/bioconductor.scm (r-transcriptr): New variable.
-rw-r--r--gnu/packages/bioconductor.scm50
1 files changed, 50 insertions, 0 deletions
diff --git a/gnu/packages/bioconductor.scm b/gnu/packages/bioconductor.scm
index 6eb34c3793..0fbe0965c2 100644
--- a/gnu/packages/bioconductor.scm
+++ b/gnu/packages/bioconductor.scm
@@ -4472,6 +4472,56 @@ this package. It also provides functionalities for visualizing, summarizing
and comparing the clusterings.")
(license license:expat)))
+(define-public r-transcriptr
+ (package
+ (name "r-transcriptr")
+ (version "1.22.0")
+ (source
+ (origin
+ (method url-fetch)
+ (uri (bioconductor-uri "transcriptR" version))
+ (sha256
+ (base32 "1p5l2z3szx3qh02x7r81ajl7yc5wqsri6q6pzw83livmalcli5yy"))))
+ (properties `((upstream-name . "transcriptR")))
+ (build-system r-build-system)
+ (propagated-inputs
+ (list r-biocgenerics
+ r-caret
+ r-chipseq
+ r-e1071
+ r-genomeinfodb
+ r-genomicalignments
+ r-genomicfeatures
+ r-genomicranges
+ r-ggplot2
+ r-iranges
+ r-proc
+ r-reshape2
+ r-rsamtools
+ r-rtracklayer
+ r-s4vectors))
+ (native-inputs (list r-knitr))
+ (home-page "https://bioconductor.org/packages/transcriptR")
+ (synopsis "Primary transcripts detection and quantification")
+ (description
+ "The differences in the RNA types being sequenced have an impact on the
+resulting sequencing profiles. mRNA-seq data is enriched with reads derived
+from exons, while GRO-, nucRNA- and chrRNA-seq demonstrate a substantial
+broader coverage of both exonic and intronic regions. The presence of
+intronic reads in GRO-seq type of data makes it possible to use it to
+computationally identify and quantify all de novo continuous regions of
+transcription distributed across the genome. This type of data, however, is
+more challenging to interpret and less common practice compared to mRNA-seq.
+One of the challenges for primary transcript detection concerns the
+simultaneous transcription of closely spaced genes, which needs to be properly
+divided into individually transcribed units. The R package transcriptR
+combines RNA-seq data with ChIP-seq data of histone modifications that mark
+active Transcription Start Sites (TSSs), such as, H3K4me3 or H3K9/14Ac to
+overcome this challenge. The advantage of this approach over the use of, for
+example, gene annotations is that this approach is data driven and therefore
+able to deal also with novel and case specific events.")
+ (license license:gpl3)))
+
(define-public r-trajectoryutils
(package
(name "r-trajectoryutils")