[med-svn] [SCM] python-htseq branch, master, updated. ed1f7a8dc669f35f339c747e1ade91a00871190d

[Diane Trout]

The following commit has been merged in the master branch:
commit ed1f7a8dc669f35f339c747e1ade91a00871190d
Author: Diane Trout <diane at ghic.org>
Date:   Thu Aug 1 22:20:19 2013 -0700

    Improve the package description

diff --git a/debian/control b/debian/control
index afa4f52..4835ba6 100644
--- a/debian/control
+++ b/debian/control
@@ -14,8 +14,9 @@ Standards-Version: 3.9.4
 Package: python-htseq
 Architecture: any
 Depends: ${misc:Depends}, ${python:Depends}, ${shlibs:Depends}
-Description: package for high-throughput genome sequencing analysis
- HTSeq can be used to performing a number of common analysis tasks:
+Description: high-throughput genome sequencing read analysis utilities
+ HTSeq can be used to performing a number of common analysis tasks
+ when working with high-throughput genome sequencing reads:
  .
    * Getting statistical summaries about the base-call quality scores to
      study the data quality.
@@ -30,15 +31,8 @@ Architecture: all
 Section: doc
 Depends: ${sphinxdoc:Depends}, ${misc:Depends}
 Description: documetation for HTSeq (high-throughput genome sequencing)
- HTSeq can be used to performing a number of common 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.
+ HTSeq can be used to performing a number of common analysis tasks
+ when working with high-throughput genome sequencing reads.
  .
  This package contains documentation in HTML form.
 

-- 
Packaging of HTSeq for Debian.