Bug#718664: ITP: htseq -- high-throughput genome sequencing analysis.

[Diane Trout <diane@ghic.org>]

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