[med-svn] r8111 - trunk/packages/sigma-align/trunk/debian

[Steffen Möller]

Author: moeller
Date: 2011-10-08 11:55:40 +0000 (Sat, 08 Oct 2011)
New Revision: 8111

Modified:
   trunk/packages/sigma-align/trunk/debian/changelog
   trunk/packages/sigma-align/trunk/debian/control
Log:
Addressing concern raised in #644663


Modified: trunk/packages/sigma-align/trunk/debian/changelog
===================================================================
--- trunk/packages/sigma-align/trunk/debian/changelog	2011-10-07 14:51:54 UTC (rev 8110)
+++ trunk/packages/sigma-align/trunk/debian/changelog	2011-10-08 11:55:40 UTC (rev 8111)
@@ -1,6 +1,7 @@
 sigma-align (1.1.3-2) UNRELEASED; urgency=low
 
   * Documented informations in ‘debian/upstream-metadata.yaml’.
+  * Split long description in two (Closes: #644663)
 
  -- Charles Plessy <plessy at debian.org>  Sun, 03 Jan 2010 19:28:49 +0900
 

Modified: trunk/packages/sigma-align/trunk/debian/control
===================================================================
--- trunk/packages/sigma-align/trunk/debian/control	2011-10-07 14:51:54 UTC (rev 8110)
+++ trunk/packages/sigma-align/trunk/debian/control	2011-10-08 11:55:40 UTC (rev 8111)
@@ -15,10 +15,12 @@
 Architecture: any
 Depends: ${shlibs:Depends}, ${misc:Depends}
 Description: Simple greedy multiple alignment of non-coding DNA sequences
- Sigma (“Simple greedy multiple alignment”) is an alignment program with a
+ Sigma (“Simple greedy multiple alignment”) is an alignment program. It has a
  new algorithm and scoring scheme designed specifically for non-coding DNA
- sequence. It uses a strategy of seeking the best possible gapless local
- alignments, at each step making the best possible alignment consistent with
- existing alignments, and scores the significance of the alignment based on
- the lengths of the aligned fragments and a background model which may be
+ sequence.
+ .
+ It uses a strategy of seeking the best possible gapless local alignments. This
+ happens at each step making the best possible alignment consistent with
+ existing alignments. It scores the significance of the alignment based on the
+ lengths of the aligned fragments and a background model. These may be
  supplied or estimated from an auxiliary file of intergenic DNA.