[med-svn] [plink1.9] 06/08: cme fix dpkg-control

Dylan Aïssi bob.dybian-guest at moszumanska.debian.org
Fri Sep 15 22:03:20 UTC 2017


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bob.dybian-guest pushed a commit to branch master
in repository plink1.9.

commit b7647abd32ece2500577d716b17156a3770ef22e
Author: Dylan Aïssi <bob.dybian at gmail.com>
Date:   Wed Sep 13 15:09:47 2017 +0200

    cme fix dpkg-control
---
 debian/changelog | 1 +
 debian/control   | 9 +++++----
 2 files changed, 6 insertions(+), 4 deletions(-)

diff --git a/debian/changelog b/debian/changelog
index 91a4c6b..12f8079 100644
--- a/debian/changelog
+++ b/debian/changelog
@@ -5,6 +5,7 @@ plink1.9 (1.90~b4.7-170906-1) UNRELEASED; urgency=medium
   * Update 01.Fix_Makefile.patch.
   * Bump Standards-Version to 4.1.0.
   * Remove Testsuite field from d/control, now automatically added.
+  * cme fix dpkg-control.
 
  -- Dylan Aïssi <bob.dybian at gmail.com>  Wed, 19 Jul 2017 23:50:02 +0200
 
diff --git a/debian/control b/debian/control
index 8cd7a94..3ffc86f 100644
--- a/debian/control
+++ b/debian/control
@@ -1,21 +1,22 @@
 Source: plink1.9
-Section: science
-Priority: optional
 Maintainer: Debian Med Packaging Team <debian-med-packaging at lists.alioth.debian.org>
 Uploaders: Dylan Aïssi <bob.dybian at gmail.com>
+Section: science
+Priority: optional
 Build-Depends: debhelper (>= 10),
                help2man,
                libatlas-base-dev,
                liblapack-dev,
                zlib1g-dev
 Standards-Version: 4.1.0
-Vcs-Browser: https://anonscm.debian.org/git/debian-med/plink1.9.git
+Vcs-Browser: https://anonscm.debian.org/cgit/debian-med/plink1.9.git
 Vcs-Git: https://anonscm.debian.org/git/debian-med/plink1.9.git
 Homepage: https://www.cog-genomics.org/plink/1.9/
 
 Package: plink1.9
 Architecture: any-amd64 any-i386 armel armhf mipsel
-Depends: ${misc:Depends}, ${shlibs:Depends}
+Depends: ${misc:Depends},
+         ${shlibs:Depends}
 Description: whole-genome association analysis toolset
  plink expects as input the data from SNP (single nucleotide polymorphism)
  chips of many individuals and their phenotypical description of a disease.

-- 
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