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authorLinlin Yan <yanlinlin82@gmail.com>2014-12-21 20:02:06 +0800
committerLinlin Yan <yanlinlin82@gmail.com>2014-12-21 20:02:06 +0800
commite1b72f907d6de13465c6d1f84a6cd588f22dacfc (patch)
treed68c35a6daf9016ee7368b7aaaeea320fe35e4cc /sci-biology/bismark
parentsci-biology/bismark: Add new package. (diff)
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sci-biology/bismark: Remove 'dodir' and break long lines.
Diffstat (limited to 'sci-biology/bismark')
-rw-r--r--sci-biology/bismark/bismark-0.13.0.ebuild1
-rw-r--r--sci-biology/bismark/metadata.xml16
2 files changed, 9 insertions, 8 deletions
diff --git a/sci-biology/bismark/bismark-0.13.0.ebuild b/sci-biology/bismark/bismark-0.13.0.ebuild
index b62a44aa2..a941da61f 100644
--- a/sci-biology/bismark/bismark-0.13.0.ebuild
+++ b/sci-biology/bismark/bismark-0.13.0.ebuild
@@ -22,7 +22,6 @@ S="${WORKDIR}/${PN}_v${PV}"
src_install() {
dobin bismark{,2bedGraph,2report,_genome_preparation,_methylation_extractor} coverage2cytosine deduplicate_bismark
- dodir /usr/share/${P}
insinto /usr/share/${P}
doins bismark_sitrep.tpl
dosym /usr/share/${P}/bismark_sitrep.tpl /usr/bin/bismark_sitrep.tpl
diff --git a/sci-biology/bismark/metadata.xml b/sci-biology/bismark/metadata.xml
index 12d2ae01b..7c23d3ec8 100644
--- a/sci-biology/bismark/metadata.xml
+++ b/sci-biology/bismark/metadata.xml
@@ -7,12 +7,14 @@
</maintainer>
<herd>sci-biology</herd>
<longdescription lang="en">
-Bismark is a program to map bisulfite treated sequencing reads to a genome of interest and perform methylation calls in a single step. The output can be easily imported into a genome viewer, such as SeqMonk, and enables a researcher to analyse the methylation levels of their samples straight away. It's main features are:
-
-Bisulfite mapping and methylation calling in one single step
-Supports single-end and paired-end read alignments
-Supports ungapped and gapped alignments
-Alignment seed length, number of mismatches etc. are adjustable
-Output discriminates between cytosine methylation in CpG, CHG and CHH context
+Bismark is a program to map bisulfite treated sequencing reads to a genome of
+interest and perform methylation calls in a single step. The output can be
+easily imported into a genome viewer, such as SeqMonk, and enables a researcher
+to analyse the methylation levels of their samples straight away. It's main
+features are: (1) Bisulfite mapping and methylation calling in one single step;
+(2) Supports single-end and paired-end read alignments; (3) Supports ungapped
+and gapped alignments; (4) Alignment seed length, number of mismatches etc. are
+adjustable; (5) Output discriminates between cytosine methylation in CpG, CHG
+and CHH context.
</longdescription>
</pkgmetadata>