deb_control_files:
- control
- md5sums
deb_fields:
Architecture: all
Depends: default-jre, libsnpsift-java (= 5.2.e+dfsg-1)
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.
Homepage: https://pcingola.github.io/SnpEff/ss_introduction/
Installed-Size: '15'
Maintainer: Debian Med Packaging Team <debian-med-packaging@lists.alioth.debian.org>
Package: snpsift
Priority: optional
Section: java
Suggests: snpeff
Version: 5.2.e+dfsg-1
srcpkg_name: snpsift
srcpkg_version: 5.2.e+dfsg-1