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authorRoel Janssen2016-03-03 21:54:02 +0100
committerRoel Janssen2016-03-03 21:54:02 +0100
commitfe3e5fe9d0924e5d1f9945f57420f342e1e312a5 (patch)
tree1c4a8edd5f64d3a98374417e84f1757f5baea0df /gn
parentb79a29c4e756450c6e34a9464a2c321c992b50a6 (diff)
downloadguix-bioinformatics-fe3e5fe9d0924e5d1f9945f57420f342e1e312a5.tar.gz
Fix for home-page, synopsis and description of vcflib.
Diffstat (limited to 'gn')
-rw-r--r--gn/packages/bioinformatics.scm15
1 files changed, 8 insertions, 7 deletions
diff --git a/gn/packages/bioinformatics.scm b/gn/packages/bioinformatics.scm
index 2ef6f2c..295a2b3 100644
--- a/gn/packages/bioinformatics.scm
+++ b/gn/packages/bioinformatics.scm
@@ -784,11 +784,12 @@ supported.")
(install-file file bin))
(find-files "bin" ".*"))
(install-file "libvcflib.a" lib)))))))
- (home-page "https://github.com/ekg/freebayes")
- (synopsis "haplotype-based variant detector.")
- (description "FreeBayes is a Bayesian genetic variant detector designed to
-find small polymorphisms, specifically SNPs (single-nucleotide polymorphisms),
-indels (insertions and deletions), MNPs (multi-nucleotide polymorphisms), and
-complex events (composite insertion and substitution events) smaller than the
-length of a short-read sequencing alignment.")
+ (home-page "https://github.com/vcflib/vcflib/")
+ (synopsis "Library for parsing and manipulating VCF files")
+ (description "Vcflib provides methods to manipulate and interpret
+sequence variation as it can be described by VCF. It is both an API for parsing
+and operating on records of genomic variation as it can be described by the VCF
+format, and a collection of command-line utilities for executing complex
+manipulations on VCF files.")
(license license:expat))))
+