[med-svn] [Git][med-team/allelecount][master] 2 commits: Add Conda ID
Andreas Tille
gitlab at salsa.debian.org
Tue May 12 10:30:57 BST 2020
Andreas Tille pushed to branch master at Debian Med / allelecount
Commits:
a346e745 by Andreas Tille at 2020-05-12T11:20:10+02:00
Add Conda ID
- - - - -
e3f44a9c by Andreas Tille at 2020-05-12T11:30:33+02:00
Provide separate Perl module package
- - - - -
6 changed files:
- + debian/allelecount.install
- debian/control
- + debian/liballelecount-perl.install
- + debian/liballelecount-perl.lintian-overrides
- debian/rules
- debian/upstream/metadata
Changes:
=====================================
debian/allelecount.install
=====================================
@@ -0,0 +1 @@
+c/bin/alleleCounter usr/bin
=====================================
debian/control
=====================================
@@ -3,6 +3,7 @@ Maintainer: Debian Med Packaging Team <debian-med-packaging at lists.alioth.debian.
Uploaders: Andreas Tille <tille at debian.org>
Section: science
Priority: optional
+Testsuite: autopkgtest-pkg-perl
Build-Depends: debhelper-compat (= 12),
libhts-dev,
libbz2-dev,
@@ -23,7 +24,19 @@ Homepage: https://github.com/cancerit/alleleCount
Package: allelecount
Architecture: any
Depends: ${shlibs:Depends},
- ${misc:Depends},
+ ${misc:Depends}
+Description: NGS copy number algorithms
+ Support code for NGS copy number algorithms. Takes a file of locations
+ and a [cr|b]am file and generates a count of coverage of each allele
+ [ACGT] at that location (given any filter settings).
+ .
+ The alleleCount package primarily exists to prevent code duplication
+ between some other projects, specifically AscatNGS and Battenberg.
+
+Package: liballelecount-perl
+Architecture: all
+Section: perl
+Depends: ${misc:Depends},
${perl:Depends},
libconst-fast-perl,
libdevel-cover-perl,
@@ -33,10 +46,13 @@ Depends: ${shlibs:Depends},
libpod-coverage-perl,
libtest-fatal-perl (>= 0.013),
libtry-tiny-perl
-Description: NGS copy number algorithms
+Description: Perl interface to NGS copy number algorithms
Support code for NGS copy number algorithms. Takes a file of locations
and a [cr|b]am file and generates a count of coverage of each allele
[ACGT] at that location (given any filter settings).
.
The alleleCount package primarily exists to prevent code duplication
between some other projects, specifically AscatNGS and Battenberg.
+ .
+ This package provided the Perl interface to alleleCounter providing
+ Sanger::CGP::AlleleCount::Genotype.
=====================================
debian/liballelecount-perl.install
=====================================
@@ -0,0 +1 @@
+debian/tmp/usr
=====================================
debian/liballelecount-perl.lintian-overrides
=====================================
@@ -0,0 +1,2 @@
+# see https://lists.debian.org/debian-med/2018/06/msg00043.html
+libalelecounter-perl: script-with-language-extension usr/bin/*.*
=====================================
debian/rules
=====================================
@@ -9,7 +9,7 @@ include /usr/share/dpkg/default.mk
export DEB_BUILD_MAINT_OPTIONS=hardening=+all
%:
- dh $@ --sourcedirectory=c
+ dh $@
override_dh_auto_clean:
dh_auto_clean --sourcedirectory=c
=====================================
debian/upstream/metadata
=====================================
@@ -1,12 +1,3 @@
-Reference:
- Author:
- Title:
- Journal:
- Year:
- Volume:
- Number:
- Pages:
- DOI:
- PMID:
- URL:
- eprint:
+Registry:
+ - Name: conda:bioconda
+ Entry: cancerit-allelecount
View it on GitLab: https://salsa.debian.org/med-team/allelecount/-/compare/9d13d8f17db49f754b389b94d8e3a7ec3cf70b80...e3f44a9c9627a27df84f7fde78f8889fe86f1e52
--
View it on GitLab: https://salsa.debian.org/med-team/allelecount/-/compare/9d13d8f17db49f754b389b94d8e3a7ec3cf70b80...e3f44a9c9627a27df84f7fde78f8889fe86f1e52
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