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-rw-r--r--gnu/packages/bioinformatics.scm35
1 files changed, 35 insertions, 0 deletions
diff --git a/gnu/packages/bioinformatics.scm b/gnu/packages/bioinformatics.scm
index 3e8fd887ee..2669942438 100644
--- a/gnu/packages/bioinformatics.scm
+++ b/gnu/packages/bioinformatics.scm
@@ -2154,6 +2154,41 @@ Python.")
;; licensed lgpl2.1+
(license (list license:expat license:lgpl2.1+))))
+(define-public python-scdamandtools
+ (package
+ (name "python-scdamandtools")
+ (version "1.0")
+ (source (origin
+ (method git-fetch)
+ (uri (git-reference
+ (url "https://github.com/KindLab/scDamAndTools")
+ (commit (string-append "v" version))))
+ (file-name (git-file-name name version))
+ (sha256
+ (base32
+ "1mblw6cn5jqik6ky8cv7ry99z6jm1i4r71pzdfl398vrwbda65gd"))))
+ (build-system pyproject-build-system)
+ (arguments
+ (list #:tests? #f)) ;there are none
+ (propagated-inputs (list python-h5py
+ python-numpy
+ python-sortedcontainers
+ python-pandas
+ python-pysam
+ python-tqdm))
+ (native-inputs (list python-cython python-pytest))
+ (home-page "https://github.com/KindLab/scDamAndTools")
+ (synopsis "Functions for processing raw scDam&T-seq data")
+ (description
+ "This is a set of functions for processing raw scDam&T-seq data.
+scDam&T-seq is a method to simultaneously measure protein-DNA interactions and
+transcription from single cells (Rooijers et al., 2019). It combines a
+DamID-based method to measure protein-DNA interactions and an adaptation of
+CEL-Seq to measure transcription. The starting point of the workflow is raw
+sequencing data and the end result are tables of UMI-unique DamID and CEL-Seq
+counts.")
+ (license license:expat)))
+
(define-public python-bioframe
(package
(name "python-bioframe")