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| author | Roel Janssen | 2016-03-03 21:54:02 +0100 |
|---|---|---|
| committer | Roel Janssen | 2016-03-03 21:54:02 +0100 |
| commit | fe3e5fe9d0924e5d1f9945f57420f342e1e312a5 (patch) | |
| tree | 1c4a8edd5f64d3a98374417e84f1757f5baea0df /gn | |
| parent | b79a29c4e756450c6e34a9464a2c321c992b50a6 (diff) | |
| download | guix-bioinformatics-fe3e5fe9d0924e5d1f9945f57420f342e1e312a5.tar.gz | |
Fix for home-page, synopsis and description of vcflib.
Diffstat (limited to 'gn')
| -rw-r--r-- | gn/packages/bioinformatics.scm | 15 |
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)))) + |