diff options
Diffstat (limited to 'gnu/packages')
-rw-r--r-- | gnu/packages/bioinformatics.scm | 22 | ||||
-rw-r--r-- | gnu/packages/cran.scm | 22 |
2 files changed, 22 insertions, 22 deletions
diff --git a/gnu/packages/bioinformatics.scm b/gnu/packages/bioinformatics.scm index 4de52f3aaa..40c6363859 100644 --- a/gnu/packages/bioinformatics.scm +++ b/gnu/packages/bioinformatics.scm @@ -9393,28 +9393,6 @@ 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 "8.0") - (source - (origin - (method url-fetch) - (uri (cran-uri "seqminer" version)) - (sha256 - (base32 - "00jzj8mwb0zaiwlifd41b26mrq9mzigj18nc29dydi0r42hxg16i")))) - (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+)))) - (define-public r-raremetals2 (package (name "r-raremetals2") diff --git a/gnu/packages/cran.scm b/gnu/packages/cran.scm index 57b68c26ed..fec9947d0d 100644 --- a/gnu/packages/cran.scm +++ b/gnu/packages/cran.scm @@ -24383,3 +24383,25 @@ Locus} (QTL) analysis in experimental crosses. It is a reimplementation of the @code{R/qtl} package to better handle high-dimensional data and complex cross designs. Broman et al. (2018) <doi:10.1534/genetics.118.301595>.") (license license:gpl3))) + +(define-public r-seqminer + (package + (name "r-seqminer") + (version "8.0") + (source + (origin + (method url-fetch) + (uri (cran-uri "seqminer" version)) + (sha256 + (base32 + "00jzj8mwb0zaiwlifd41b26mrq9mzigj18nc29dydi0r42hxg16i")))) + (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+)))) |