Package: snpsift
Version: 5.4.b+dfsg-1
Architecture: all
Maintainer: Ubuntu Developers <ubuntu-devel-discuss@lists.ubuntu.com>
Original-Maintainer: Debian Med Packaging Team <debian-med-packaging@lists.alioth.debian.org>
Installed-Size: 15
Depends: default-jre, libsnpsift-java (= 5.4.b+dfsg-1)
Suggests: snpeff
Section: java
Priority: optional
Homepage: https://pcingola.github.io/SnpEff/ss_introduction/
Description: tool to annotate and manipulate genome variants - tool
 SnpSift is a toolbox that allows one to filter and manipulate annotated files.
 Once the genomic variants have been annotated, one needs to filter them out in
 order to find the "interesting / relevant variants". Given the large data
 files, this is not a trivial task (e.g. one cannot load all the variants into
 XLS spreadsheet). SnpSift helps to perform this VCF file manipulation and
 filtering required at this stage in data processing pipelines.
 .
 This package contains the command line tool.
