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| author | Ricardo Wurmus <rekado@elephly.net> | 2017-01-16 11:59:24 +0100 |
|---|---|---|
| committer | Ricardo Wurmus <rekado@elephly.net> | 2017-01-17 21:46:48 +0100 |
| commit | fb1e528ef1edca46ba4152b88356266944982ebe (patch) | |
| tree | 696c20e4b58cf613ed24d66654a50dc998ce4ddb /gnu/packages | |
| parent | 26a281ef27efc9011fbe7cd42a4c0be82e013fcb (diff) | |
| download | guix-fb1e528ef1edca46ba4152b88356266944982ebe.tar.gz | |
gnu: Add r-seqminer.
* gnu/packages/bioinformatics.scm (r-seqminer): New variable.
Diffstat (limited to 'gnu/packages')
| -rw-r--r-- | gnu/packages/bioinformatics.scm | 22 |
1 files changed, 22 insertions, 0 deletions
diff --git a/gnu/packages/bioinformatics.scm b/gnu/packages/bioinformatics.scm index cd64d34390..28a0da80e8 100644 --- a/gnu/packages/bioinformatics.scm +++ b/gnu/packages/bioinformatics.scm @@ -8149,3 +8149,25 @@ high-dimensional data like gene expression/RNA sequencing/methylation/brain imaging data that can be used in subsequent analyses to adjust for unknown, unmodeled, or latent sources of noise.") (license license:artistic2.0))) + +(define-public r-seqminer + (package + (name "r-seqminer") + (version "5.3") + (source + (origin + (method url-fetch) + (uri (cran-uri "seqminer" version)) + (sha256 + (base32 + "0y0gc5lws3hdxasjb84m532ics6imb7qg9sl1zy62h503jh4j9gw")))) + (build-system r-build-system) + (inputs + `(("zlib" ,zlib))) + (home-page "http://seqminer.genomic.codes") + (synopsis "Read nucleotide sequence data (VCF, BCF, and METAL formats)") + (description + "This package provides tools to integrate nucleotide sequencing +data (variant call format, e.g. VCF or BCF) or meta-analysis results in R.") + ;; Any version of the GPL is acceptable + (license (list license:gpl2+ license:gpl3+)))) |