[med-svn] [SCM] gmap branch, master, updated. upstream/2012-06-12-19-gbb6db31

[Andreas Tille]

The following commit has been merged in the master branch:
commit b00908b4d20e33bbc9e1bf409664fe3ac9496ec1
Author: Andreas Tille <tille at debian.org>
Date:   Fri Aug 2 15:12:00 2013 +0200

    cme fix dpkg-control

diff --git a/debian/changelog b/debian/changelog
index c8f5330..200845a 100644
--- a/debian/changelog
+++ b/debian/changelog
@@ -1,6 +1,7 @@
 gmap (2013-07-20-1) UNRELEASED; urgency=low
 
   * New upstream version
+  * debian/control: cme fix dpkg-control
 
  -- Andreas Tille <tille at debian.org>  Fri, 02 Aug 2013 15:09:36 +0200
 
diff --git a/debian/control b/debian/control
index 5dce776..702a83f 100644
--- a/debian/control
+++ b/debian/control
@@ -1,19 +1,21 @@
 Source: gmap
-Section: non-free/science
-Priority: optional
 Maintainer: Debian Med Packaging Team <debian-med-packaging at lists.alioth.debian.org>
-DM-Upload-Allowed: yes
 Uploaders: Shaun Jackman <sjackman at debian.org>,
- Andreas Tille <tille at debian.org>
-Build-Depends: debhelper (>= 8), autotools-dev
-Standards-Version: 3.9.3
-Homepage: http://research-pub.gene.com/gmap/
-Vcs-Git: git://git.debian.org/git/debian-med/gmap.git
+           Andreas Tille <tille at debian.org>
+Section: non-free/science
+Priority: optional
+Build-Depends: debhelper (>= 8),
+               autotools-dev
+Standards-Version: 3.9.4
 Vcs-Browser: http://git.debian.org/?p=debian-med/gmap.git
+Vcs-Git: git://git.debian.org/git/debian-med/gmap.git
+Homepage: http://research-pub.gene.com/gmap/
 
 Package: gmap
 Architecture: any
-Depends: ${shlibs:Depends}, ${misc:Depends}, ${perl:Depends}
+Depends: ${shlibs:Depends},
+         ${misc:Depends},
+         ${perl:Depends}
 Description: spliced and SNP-tolerant alignment for mRNA and short reads
  This package contains the programs GMAP and GSNAP as well as
  utilities to manage genome databases in GMAP/GSNAP format.
@@ -22,6 +24,7 @@ Description: spliced and SNP-tolerant alignment for mRNA and short reads
  GSNAP (Genomic Short-read Nucleotide Alignment Program) is a tool for
  aligning single-end and paired-end transcriptome reads.
  Both tools can use a database of
- * known splice sites and identify novel splice sites.
- * known single-nucleotide polymorphisms (SNPs).
+  * known splice sites and identify novel splice sites.
+  * known single-nucleotide polymorphisms (SNPs).
  GSNAP can align bisulfite-treated DNA.
+

-- 
Align mRNA and EST sequences to a genome