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gnu: cnvkit: Update to 0.9.12.
* gnu/packages/bioinformatics.scm (cnvkit): Update to 0.9.12. [build-system]: Switch to pyproject. [native-inputs]: Add python-setuptools, python-wheel. Change-Id: Ia48f681ac2c45872c92214d685819579a40eae7a Signed-off-by: Steve George <steve@futurile.net>
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1 changed files with 3 additions and 3 deletions
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@ -21217,7 +21217,7 @@ polymorphisms) and indels with respect to a reference genome and more.")
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(define-public cnvkit
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(package
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(name "cnvkit")
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(version "0.9.10")
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(version "0.9.12")
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(source
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(origin
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(method git-fetch)
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@ -21226,7 +21226,7 @@ polymorphisms) and indels with respect to a reference genome and more.")
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(commit (string-append "v" version))))
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(file-name (git-file-name name version))
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(sha256
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(base32 "0r303pqjg70zpxa564bavbfj99c6di0dafgqqwx2vh4vfsiif94q"))))
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(base32 "090yh17symcahddx399kcx0mcw4gdrcc2jil3p8lb92r8c8kglb5"))))
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(build-system pyproject-build-system)
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(propagated-inputs
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(list python-biopython
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@ -21243,7 +21243,7 @@ polymorphisms) and indels with respect to a reference genome and more.")
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;; R packages
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r-dnacopy))
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(inputs (list r-minimal)) ;for tests
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(native-inputs (list python-setuptools python-wheel))
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(native-inputs (list python-pytest python-setuptools python-wheel))
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(home-page "https://cnvkit.readthedocs.org/")
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(synopsis "Copy number variant detection from targeted DNA sequencing")
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(description
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