Bug#718664: ITP: htseq -- high-throughput genome sequencing analysis.
Package: wnpp
Severity: wishlist
Owner: Diane Trout <diane@ghic.org>
X-Debbugs-CC: debian-med@lists.debian.org, debian-devel@lists.debian.org
Package name: htseq
Version: 0.5.4p3
Upstream Author: Simon Anders <sanders@fs.tum.de>
URL: http://www-huber.embl.de/users/anders/HTSeq/doc/overview.html
License: GPL-3+
Programming Lang: Python
Description: HTSeq can be used for a number of common high-throughput
genomics analysis tasks.
.
* Getting statistical summaries about the base-call quality scores to
study the data quality.
* Calculating a coverage vector and exporting it for visualization in
a genome browser.
* Reading in annotation data from a GFF file.
* Assigning aligned reads from an RNA-Seq experiments to exons and
genes.
Remark: This package is maintained in the Debian Med team and available in VCS
at: git://git.debian.org/debian-med/python-htseq.git
Reply to: