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-rw-r--r--gnu/packages/bioinformatics.scm45
1 files changed, 45 insertions, 0 deletions
diff --git a/gnu/packages/bioinformatics.scm b/gnu/packages/bioinformatics.scm
index ad950b4090..4ef4f6788f 100644
--- a/gnu/packages/bioinformatics.scm
+++ b/gnu/packages/bioinformatics.scm
@@ -2583,6 +2583,51 @@ cell types and subtypes.")
and sequence consensus.")
(license license:expat)))
+(define-public python-cnmf
+ (package
+ (name "python-cnmf")
+ (version "1.6.0")
+ (source
+ (origin
+ (method url-fetch)
+ (uri (pypi-uri "cnmf" version))
+ (sha256
+ (base32 "0aic8cwj6riykcfgl6v2x3si5z04gaknkh5a8lcyv1qh4s1gx3d3"))))
+ (build-system pyproject-build-system)
+ (arguments
+ (list
+ #:tests? #f ; no tests in git checkout and PyPI archive
+ #:phases
+ #~(modify-phases %standard-phases
+ (add-after 'unpack 'set-envs
+ (lambda _
+ (setenv "MPLCONFIGDIR" "/tmp")
+ ;; Numba needs a writable dir to cache functions.
+ (setenv "NUMBA_CACHE_DIR" "/tmp"))))))
+ (native-inputs
+ (list python-setuptools
+ python-wheel))
+ (propagated-inputs
+ (list python-anndata
+ python-fastcluster
+ python-matplotlib
+ python-numba
+ python-numpy
+ python-palettable
+ python-pandas
+ python-pyyaml
+ python-scanpy
+ python-scikit-learn
+ python-scipy))
+ (home-page "https://github.com/dylkot/cNMF")
+ (synopsis "Consensus NMF for scRNA-Seq data")
+ (description
+ "This tool offers a pipeline for inferring gene expression programs from
+scRNA-Seq. It takes a count matrix (N cells X G genes) as input and produces
+a (K x G) matrix of gene expression programs (GEPs) and a (N x K) matrix
+specifying the usage of each program for each cell in the data.")
+ (license license:expat)))
+
(define-public python-cyvcf2
(package
(name "python-cyvcf2")