@@ 21217,7 21217,7 @@ polymorphisms) and indels with respect to a reference genome and more.")
(define-public cnvkit
(package
(name "cnvkit")
- (version "0.9.10")
+ (version "0.9.12")
(source
(origin
(method git-fetch)
@@ 21226,7 21226,7 @@ polymorphisms) and indels with respect to a reference genome and more.")
(commit (string-append "v" version))))
(file-name (git-file-name name version))
(sha256
- (base32 "0r303pqjg70zpxa564bavbfj99c6di0dafgqqwx2vh4vfsiif94q"))))
+ (base32 "090yh17symcahddx399kcx0mcw4gdrcc2jil3p8lb92r8c8kglb5"))))
(build-system pyproject-build-system)
(propagated-inputs
(list python-biopython
@@ 21243,7 21243,7 @@ polymorphisms) and indels with respect to a reference genome and more.")
;; R packages
r-dnacopy))
(inputs (list r-minimal)) ;for tests
- (native-inputs (list python-setuptools python-wheel))
+ (native-inputs (list python-pytest python-setuptools python-wheel))
(home-page "https://cnvkit.readthedocs.org/")
(synopsis "Copy number variant detection from targeted DNA sequencing")
(description