Package: libsnpsift-java
Source: snpsift
Version: 5.2.e+dfsg-2build1
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: 408
Depends: antlr4, libcommons-math3-java (>= 3.6.1), libhtsjdk-java (>= 4.1.3), libsnpeff-java, libtrove3-java
Section: java
Priority: optional
Homepage: https://pcingola.github.io/SnpEff/ss_introduction/
Description: tool to annotate and manipulate genome variants - lib
 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 library.
