[med-svn] [maffilter] 01/01: No leading spaces in long description

[Andreas Tille]

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tille pushed a commit to branch master
in repository maffilter.

commit 4028d964d549d11c60230c1bc4d01662b0a66b5c
Author: Andreas Tille <tille at debian.org>
Date:   Sat Apr 23 19:39:07 2016 +0200

    No leading spaces in long description
---
 debian/control | 26 +++++++++++++-------------
 1 file changed, 13 insertions(+), 13 deletions(-)

diff --git a/debian/control b/debian/control
index ba79ce9..8be3484 100644
--- a/debian/control
+++ b/debian/control
@@ -21,17 +21,17 @@ Architecture: any
 Depends: ${shlibs:Depends},
          ${misc:Depends}
 Description: process genome alignment in the Multiple Alignment Format
-  MafFilter applies a series of "filters" to a MAF file, in order to
-  clean it, extract data and computer statistics while keeping track of
-  the associated meta-data such as genome coordinates and quality scores.
+ MafFilter applies a series of "filters" to a MAF file, in order to
+ clean it, extract data and computer statistics while keeping track of
+ the associated meta-data such as genome coordinates and quality scores.
  .
-   * It can process the alignment to remove low-quality / ambiguous /
-     masked regions.
-   * It can export data into a single or multiple alignment file in
-     format such as Fasta or Clustal.
-   * It can read annotation data in GFF or GTF format, and extract the
-     corresponding alignment.
-   * It can perform sliding windows calculations.
-   * It can reconstruct phylogeny/genealogy along the genome alignment.
-   * It can compute population genetics statistics, such as site
-     frequency spectrum, number of fixed/polymorphic sites, etc.
+  * It can process the alignment to remove low-quality / ambiguous /
+    masked regions.
+  * It can export data into a single or multiple alignment file in
+    format such as Fasta or Clustal.
+  * It can read annotation data in GFF or GTF format, and extract the
+    corresponding alignment.
+  * It can perform sliding windows calculations.
+  * It can reconstruct phylogeny/genealogy along the genome alignment.
+  * It can compute population genetics statistics, such as site
+    frequency spectrum, number of fixed/polymorphic sites, etc.

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