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gnu: r-seqminer: Move to (gnu packages cran).

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* 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>
This commit is contained in:
zimoun 2020-09-11 20:08:44 +02:00 committed by Ricardo Wurmus
parent 66a8e62070
commit 30aaee3306
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GPG Key ID: 197A5888235FACAC
2 changed files with 22 additions and 22 deletions
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22
gnu/packages/bioinformatics.scm
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@ -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")

22
gnu/packages/cran.scm
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@ -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+))))