gnu: Add deeptools.
* gnu/packages/bioinformatics.scm (deeptools): New variable.
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@ -875,6 +875,45 @@ file formats including SAM/BAM, Wiggle/BigWig, BED, GFF/GTF, VCF.")
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other types of unwanted sequence from high-throughput sequencing reads.")
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other types of unwanted sequence from high-throughput sequencing reads.")
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(license license:expat)))
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(license license:expat)))
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(define-public deeptools
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(package
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(name "deeptools")
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(version "1.5.11")
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(source (origin
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(method url-fetch)
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(uri (string-append
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"https://github.com/fidelram/deepTools/archive/"
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version ".tar.gz"))
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(file-name (string-append name "-" version ".tar.gz"))
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(sha256
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(base32
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"1kaagygcbvjs9sxd9cqmskd02wcfp9imvb735r087w7hwqpvz6fs"))))
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(build-system python-build-system)
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(arguments
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`(#:python ,python-2))
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(propagated-inputs
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`(("python-scipy" ,python2-scipy)
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("python-numpy" ,python2-numpy)
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("python-matplotlib" ,python2-matplotlib)
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("python-bx-python" ,python2-bx-python)
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("python-pysam" ,python2-pysam)))
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(native-inputs
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`(("python-mock" ,python2-mock) ;for tests
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("python-pytz" ,python2-pytz) ;for tests
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("python-setuptools" ,python2-setuptools)))
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(home-page "https://github.com/fidelram/deepTools")
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(synopsis "Tools for normalizing and visualizing deep-sequencing data")
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(description
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"DeepTools addresses the challenge of handling the large amounts of data
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that are now routinely generated from DNA sequencing centers. To do so,
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deepTools contains useful modules to process the mapped reads data to create
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coverage files in standard bedGraph and bigWig file formats. By doing so,
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deepTools allows the creation of normalized coverage files or the comparison
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between two files (for example, treatment and control). Finally, using such
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normalized and standardized files, multiple visualizations can be created to
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identify enrichments with functional annotations of the genome.")
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(license license:gpl3+)))
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(define-public diamond
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(define-public diamond
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(package
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(package
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(name "diamond")
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(name "diamond")
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