gnu: Add pigx-rnaseq.
* gnu/packages/bioinformatics.scm (pigx-rnaseq): New variable.
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@ -12646,3 +12646,70 @@ contains
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analyze RNA expression genome-wide in thousands of individual cells at
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once. This package provides tools to perform Drop-seq analyses.")
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(license license:expat)))
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(define-public pigx-rnaseq
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(package
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(name "pigx-rnaseq")
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(version "0.0.2")
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(source (origin
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(method url-fetch)
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(uri (string-append "https://github.com/BIMSBbioinfo/pigx_rnaseq/"
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"releases/download/v" version
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"/pigx_rnaseq-" version ".tar.gz"))
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(sha256
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(base32
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"168hx2ig3rarphx3l21ay9yyg8ipaakzixnrhpbdi0sknhyvrrk8"))))
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(build-system gnu-build-system)
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(arguments
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`(#:parallel-tests? #f ; not supported
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#:phases
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(modify-phases %standard-phases
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(add-after 'install 'wrap-executable
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;; Make sure the executable finds all R modules.
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(lambda* (#:key inputs outputs #:allow-other-keys)
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(let ((out (assoc-ref outputs "out")))
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(wrap-program (string-append out "/bin/pigx-rnaseq")
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`("R_LIBS_SITE" ":" = (,(getenv "R_LIBS_SITE")))
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`("PYTHONPATH" ":" = (,(getenv "PYTHONPATH")))))
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#t)))))
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(inputs
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`(("snakemake" ,snakemake)
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("fastqc" ,fastqc)
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("multiqc" ,multiqc)
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("star" ,star)
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("trim-galore" ,trim-galore)
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("htseq" ,htseq)
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("samtools" ,samtools)
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("bedtools" ,bedtools)
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("r-minimal" ,r-minimal)
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("r-rmarkdown" ,r-rmarkdown)
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("r-ggplot2" ,r-ggplot2)
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("r-ggrepel" ,r-ggrepel)
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("r-gprofiler" ,r-gprofiler)
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("r-deseq2" ,r-deseq2)
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("r-dt" ,r-dt)
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("r-knitr" ,r-knitr)
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("r-pheatmap" ,r-pheatmap)
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("r-corrplot" ,r-corrplot)
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("r-reshape2" ,r-reshape2)
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("r-plotly" ,r-plotly)
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("r-scales" ,r-scales)
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("r-summarizedexperiment" ,r-summarizedexperiment)
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("r-crosstalk" ,r-crosstalk)
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("r-tximport" ,r-tximport)
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("r-rtracklayer" ,r-rtracklayer)
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("r-rjson" ,r-rjson)
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("salmon" ,salmon)
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("ghc-pandoc" ,ghc-pandoc)
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("ghc-pandoc-citeproc" ,ghc-pandoc-citeproc)
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("python-wrapper" ,python-wrapper)
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("python-pyyaml" ,python-pyyaml)))
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(home-page "http://bioinformatics.mdc-berlin.de/pigx/")
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(synopsis "Analysis pipeline for RNA sequencing experiments")
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(description "PiGX RNAseq is an analysis pipeline for preprocessing and
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reporting for RNA sequencing experiments. It is easy to use and produces high
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quality reports. The inputs are reads files from the sequencing experiment,
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and a configuration file which describes the experiment. In addition to
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quality control of the experiment, the pipeline produces a differential
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expression report comparing samples in an easily configurable manner.")
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(license license:gpl3+)))
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