gnu: Add r-transcriptr.

* gnu/packages/bioconductor.scm (r-transcriptr): New variable.
This commit is contained in:
Ricardo Wurmus 2022-01-11 14:47:36 +01:00
parent 81ab201626
commit 61a1c3f72d
No known key found for this signature in database
GPG Key ID: 197A5888235FACAC
1 changed files with 50 additions and 0 deletions

View File

@ -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")