Andreas Tille pushed to branch master at Debian Med / segemehl


Commits:
79e2eadf by Andreas Tille at 2019-11-18T21:59:31Z
Fix typo in long description

- - - - -
d1f1b4b5 by Andreas Tille at 2019-11-18T21:59:47Z
debhelper-compat 12

- - - - -
42f7f367 by Andreas Tille at 2019-11-18T21:59:50Z
Standards-Version: 4.4.1

- - - - -
30fdb1b9 by Andreas Tille at 2019-11-18T22:01:15Z
Upload to unstable

- - - - -


3 changed files:

- debian/changelog
- − debian/compat
- debian/control


Changes:

=====================================
debian/changelog
=====================================
@@ -1,3 +1,12 @@
+segemehl (0.3.4-2) unstable; urgency=medium
+
+  * Fix typo in long description
+    Closes: #945040
+  * debhelper-compat 12
+  * Standards-Version: 4.4.1
+
+ -- Andreas Tille <[email protected]>  Mon, 18 Nov 2019 22:59:53 +0100
+
 segemehl (0.3.4-1) unstable; urgency=medium
 
   * New upstream version


=====================================
debian/compat deleted
=====================================
@@ -1 +0,0 @@
-12


=====================================
debian/control
=====================================
@@ -3,12 +3,12 @@ Maintainer: Debian Med Packaging Team 
<[email protected].
 Uploaders: Andreas Tille <[email protected]>
 Section: science
 Priority: optional
-Build-Depends: debhelper (>= 12~),
+Build-Depends: debhelper-compat (= 12),
                pkg-config,
                libhts-dev,
                libncurses-dev,
                zlib1g-dev
-Standards-Version: 4.3.0
+Standards-Version: 4.4.1
 Vcs-Browser: https://salsa.debian.org/med-team/segemehl
 Vcs-Git: https://salsa.debian.org/med-team/segemehl.git
 Homepage: http://www.bioinf.uni-leipzig.de/Software/segemehl/
@@ -20,7 +20,7 @@ Depends: ${shlibs:Depends},
 Description: short read mapping with gaps
  Segemehl is a software to map short sequencer reads to reference
  genomes. Segemehl implements a matching strategy based on enhanced
- suffix arrays (ESA). Segemehl accepts fasta and fastq queries (gzip’ed
+ suffix arrays (ESA). Segemehl accepts fasta and fastq queries (gzip'ed
  and bgzip'ed). In addition to the alignment of reads from standard DNA-
  and RNA-seq protocols, it also allows the mapping of bisulfite converted
  reads (Lister and Cokus) and implements a split read mapping strategy.



View it on GitLab: 
https://salsa.debian.org/med-team/segemehl/compare/cdf0e4e5fdf12459a97d86b589e48aa70c5018dd...30fdb1b972aa2f8dd1f2725209da124b99e3a57a

-- 
View it on GitLab: 
https://salsa.debian.org/med-team/segemehl/compare/cdf0e4e5fdf12459a97d86b589e48aa70c5018dd...30fdb1b972aa2f8dd1f2725209da124b99e3a57a
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