gnu: Add ParDRe.
* gnu/packages/bioinformatics.scm (pardre): New variable.
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@ -3885,6 +3885,47 @@ Needleman-Wunsch).")
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;; Dual licensed; also includes public domain source.
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(license (list license:gpl3 license:bsd-2))))
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(define-public pardre
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(package
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(name "pardre")
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(version "1.1.5")
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(source
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(origin
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(method url-fetch)
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(uri (string-append "mirror://sourceforge/pardre/ParDRe-rel"
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version ".tar.gz"))
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(sha256
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(base32
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"0zkyjzv4s8q2h5npalhirbk17r5b1h0n2a42mh7njzlf047h9bhy"))))
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(build-system gnu-build-system)
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(arguments
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`(#:tests? #f ; no tests included
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#:phases
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(modify-phases %standard-phases
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(delete 'configure)
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(replace 'install
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(lambda* (#:key outputs #:allow-other-keys)
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(let ((bin (string-append (assoc-ref outputs "out") "/bin")))
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(mkdir-p bin)
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(install-file "ParDRe" bin)
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#t))))))
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(inputs
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`(("openmpi" ,openmpi)
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("zlib" ,zlib)))
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(synopsis "Parallel tool to remove duplicate DNA reads")
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(description
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"ParDRe is a parallel tool to remove duplicate genetic sequence reads.
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Duplicate reads can be seen as identical or nearly identical sequences with
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some mismatches. This tool lets users avoid the analysis of unnecessary
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reads, reducing the time of subsequent procedures with the
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dataset (e.g. assemblies, mappings, etc.). The tool is implemented with MPI
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in order to exploit the parallel capabilities of multicore clusters. It is
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faster than multithreaded counterparts (end of 2015) for the same number of
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cores and, thanks to the message-passing technology, it can be executed on
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clusters.")
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(home-page "https://sourceforge.net/projects/pardre/")
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(license license:gpl3+)))
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(define-public bio-locus
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(package
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(name "bio-locus")
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