gnu: Add r-basicstarrseq.
* gnu/packages/bioconductor.scm (r-basicstarrseq): New variable. Change-Id: I88f314877ea4ab98976820a4acc337ae3a34e604
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@ -22672,6 +22672,41 @@ Additionally, BASiCS can compare gene expression patterns between two or more
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pre-specified groups of cells.")
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(license license:gpl3)))
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(define-public r-basicstarrseq
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(package
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(name "r-basicstarrseq")
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(version "1.30.0")
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(source
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(origin
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(method url-fetch)
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(uri (bioconductor-uri "BasicSTARRseq" version))
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(sha256
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(base32 "1dw6bv1qk2bn0l3m458sqgvm3s1karh4n3431pl7r0jj2r3mr6xa"))))
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(properties `((upstream-name . "BasicSTARRseq")))
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(build-system r-build-system)
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(propagated-inputs
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(list r-genomeinfodb
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r-genomicalignments
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r-genomicranges
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r-iranges
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r-s4vectors))
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(native-inputs (list r-knitr))
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(home-page "https://bioconductor.org/packages/BasicSTARRseq")
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(synopsis "Basic peak calling on STARR-seq data")
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(description
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"This package implements a method that aims to identify enhancers on
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large scale. The STARR-seq data consists of two sequencing datasets of the
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same targets in a specifc genome. The input sequences show which regions
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where tested for enhancers. Significant enriched peaks i.e. a lot more
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sequences in one region than in the input where enhancers in the genomic DNA
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are, can be identified. So the approach pursued is to call peak every region
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in which there is a lot more
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(significant in a binomial model) STARR-seq signal than input signal and
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propose an enhancer at that very same position. Enhancers then are called
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weak or strong dependent of there degree of enrichment in comparison to
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input.")
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(license license:lgpl3)))
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(define-public r-basilisk-utils
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(package
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(name "r-basilisk-utils")
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