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authorRicardo Wurmus <rekado@elephly.net>2021-02-18 15:55:57 +0100
committerRicardo Wurmus <rekado@elephly.net>2021-02-18 15:57:52 +0100
commit89d7c8efc62c7b445ee6cf9a33b69abf47d60a33 (patch)
treeb172dc7cce425217f4e7a660f638a3a6bf1e6ffe
parentff4b952325fef5e1b7f1550ce10617d76e684c63 (diff)
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gnu: Add r-chromvar.
* gnu/packages/bioconductor.scm (r-chromvar): New variable.
-rw-r--r--gnu/packages/bioconductor.scm47
1 files changed, 47 insertions, 0 deletions
diff --git a/gnu/packages/bioconductor.scm b/gnu/packages/bioconductor.scm
index a98971e294..a4d97fad65 100644
--- a/gnu/packages/bioconductor.scm
+++ b/gnu/packages/bioconductor.scm
@@ -9006,6 +9006,53 @@ provides a wrapper of de novo motif discovery software.")
This package wraps C++ code from the MOODS motif calling library.")
(license license:gpl3)))
+(define-public r-chromvar
+ (package
+ (name "r-chromvar")
+ (version "1.12.0")
+ (source
+ (origin
+ (method url-fetch)
+ (uri (bioconductor-uri "chromVAR" version))
+ (sha256
+ (base32 "0dn04ijgq8fncn2bkvnd0lnabjg2s4mpb91b3kwvv3nkgjgfx819"))))
+ (properties `((upstream-name . "chromVAR")))
+ (build-system r-build-system)
+ (propagated-inputs
+ `(("r-biocgenerics" ,r-biocgenerics)
+ ("r-biocparallel" ,r-biocparallel)
+ ("r-biostrings" ,r-biostrings)
+ ("r-bsgenome" ,r-bsgenome)
+ ("r-dt" ,r-dt)
+ ("r-genomeinfodb" ,r-genomeinfodb)
+ ("r-genomicranges" ,r-genomicranges)
+ ("r-ggplot2" ,r-ggplot2)
+ ("r-iranges" ,r-iranges)
+ ("r-matrix" ,r-matrix)
+ ("r-miniui" ,r-miniui)
+ ("r-nabor" ,r-nabor)
+ ("r-plotly" ,r-plotly)
+ ("r-rcolorbrewer" ,r-rcolorbrewer)
+ ("r-rcpp" ,r-rcpp)
+ ("r-rcpparmadillo" ,r-rcpparmadillo)
+ ("r-rsamtools" ,r-rsamtools)
+ ("r-rtsne" ,r-rtsne)
+ ("r-s4vectors" ,r-s4vectors)
+ ("r-shiny" ,r-shiny)
+ ("r-summarizedexperiment" ,r-summarizedexperiment)
+ ("r-tfbstools" ,r-tfbstools)))
+ (native-inputs `(("r-knitr" ,r-knitr)))
+ (home-page "https://bioconductor.org/packages/release/bioc/html/chromVAR.html")
+ (synopsis "Determine chromatin variation across regions")
+ (description
+ "This package @code{r-chromvar} determines variation in chromatin
+accessibility across sets of annotations or peaks. @code{r-chromvar} is
+designed primarily for single-cell or sparse chromatin accessibility data like
+single cell assay for transposase-accessible chromatin using
+sequencing (@code{scATAC-seq} or sparse bulk ATAC or deoxyribonuclease
+sequence (@code{DNAse-seq}) experiments.")
+ (license license:expat)))
+
(define-public r-singlecellexperiment
(package
(name "r-singlecellexperiment")