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-rw-r--r--gnu/packages/bioinformatics.scm24
1 files changed, 24 insertions, 0 deletions
diff --git a/gnu/packages/bioinformatics.scm b/gnu/packages/bioinformatics.scm
index c13e6499b7..b64dab73cd 100644
--- a/gnu/packages/bioinformatics.scm
+++ b/gnu/packages/bioinformatics.scm
@@ -311,6 +311,30 @@ several alignment strategies enable effective alignment of RNA-seq reads, in
particular, reads spanning multiple exons.")
(license license:gpl3+)))
+(define-public htseq
+ (package
+ (name "htseq")
+ (version "0.6.1")
+ (source (origin
+ (method url-fetch)
+ (uri (string-append
+ "https://pypi.python.org/packages/source/H/HTSeq/HTSeq-"
+ version ".tar.gz"))
+ (sha256
+ (base32
+ "1i85ppf2j2lj12m0x690qq5nn17xxk23pbbx2c83r8ayb5wngzwv"))))
+ (build-system python-build-system)
+ (arguments `(#:python ,python-2)) ; only Python 2 is supported
+ (inputs
+ `(("python-numpy" ,python2-numpy)
+ ("python-setuptools" ,python2-setuptools)))
+ (home-page "http://www-huber.embl.de/users/anders/HTSeq/")
+ (synopsis "Analysing high-throughput sequencing data with Python")
+ (description
+ "HTSeq is a Python package that provides infrastructure to process data
+from high-throughput sequencing assays.")
+ (license license:gpl3+)))
+
(define-public rseqc
(package
(name "rseqc")