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author | Ricardo Wurmus <rekado@elephly.net> | 2019-03-29 15:40:22 +0100 |
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committer | Ricardo Wurmus <rekado@elephly.net> | 2019-03-29 17:13:45 +0100 |
commit | 32e0f906d775679d8b4e770d267d29cb77724360 (patch) | |
tree | 5b9d1068e9f6ddb6a04f48c200f76182c646197b /gnu/packages | |
parent | e5bff3079d673d1d7816b0c30142935ef1e05791 (diff) |
gnu: Add r-atacseqqc.
* gnu/packages/bioconductor.scm (r-atacseqqc): New variable.
Diffstat (limited to 'gnu/packages')
-rw-r--r-- | gnu/packages/bioconductor.scm | 44 |
1 files changed, 44 insertions, 0 deletions
diff --git a/gnu/packages/bioconductor.scm b/gnu/packages/bioconductor.scm index 0daea685e5..4ee14a4c08 100644 --- a/gnu/packages/bioconductor.scm +++ b/gnu/packages/bioconductor.scm @@ -3302,3 +3302,47 @@ type and symbol colors.") "This package provides infrastructure to store and access genome-wide position-specific scores within R and Bioconductor.") (license license:artistic2.0))) + +(define-public r-atacseqqc + (package + (name "r-atacseqqc") + (version "1.6.4") + (source + (origin + (method url-fetch) + (uri (bioconductor-uri "ATACseqQC" version)) + (sha256 + (base32 + "1rblvqar11fib6ip2hq0756vqi6qmncf90jw6i5p5lrgzmaxy8hn")))) + (properties `((upstream-name . "ATACseqQC"))) + (build-system r-build-system) + (propagated-inputs + `(("r-biocgenerics" ,r-biocgenerics) + ("r-biostrings" ,r-biostrings) + ("r-bsgenome" ,r-bsgenome) + ("r-chippeakanno" ,r-chippeakanno) + ("r-genomeinfodb" ,r-genomeinfodb) + ("r-genomicalignments" ,r-genomicalignments) + ("r-genomicranges" ,r-genomicranges) + ("r-genomicscores" ,r-genomicscores) + ("r-iranges" ,r-iranges) + ("r-kernsmooth" ,r-kernsmooth) + ("r-limma" ,r-limma) + ("r-motifstack" ,r-motifstack) + ("r-preseqr" ,r-preseqr) + ("r-randomforest" ,r-randomforest) + ("r-rsamtools" ,r-rsamtools) + ("r-rtracklayer" ,r-rtracklayer) + ("r-s4vectors" ,r-s4vectors))) + (home-page "https://bioconductor.org/packages/ATACseqQC/") + (synopsis "ATAC-seq quality control") + (description + "ATAC-seq, an assay for Transposase-Accessible Chromatin using +sequencing, is a rapid and sensitive method for chromatin accessibility +analysis. It was developed as an alternative method to MNase-seq, FAIRE-seq +and DNAse-seq. The ATACseqQC package was developed to help users to quickly +assess whether their ATAC-seq experiment is successful. It includes +diagnostic plots of fragment size distribution, proportion of mitochondria +reads, nucleosome positioning pattern, and CTCF or other Transcript Factor +footprints.") + (license license:gpl2+))) |