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authorzimoun <zimon.toutoune@gmail.com>2020-09-11 20:08:44 +0200
committerRicardo Wurmus <rekado@elephly.net>2020-09-11 21:59:07 +0200
commit30aaee33066b9479cfc353f97f5f83f2e64517ef (patch)
tree8cc5abdb42e74a5f9490586ff6bbbc7117bb9d81
parent66a8e620705d98b6240670f7f5f9441462e8f621 (diff)
downloadguix-30aaee33066b9479cfc353f97f5f83f2e64517ef.tar
guix-30aaee33066b9479cfc353f97f5f83f2e64517ef.tar.gz
gnu: r-seqminer: Move to (gnu packages cran).
* gnu/packages/bioinformatics.scm (r-seqminer): Move from here... * gnu/packages/cran.scm (r-seqminer): ...to here. Signed-off-by: Ricardo Wurmus <rekado@elephly.net>
-rw-r--r--gnu/packages/bioinformatics.scm22
-rw-r--r--gnu/packages/cran.scm22
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+))))