deb_control_files:
- control
- md5sums
deb_fields:
Architecture: all
Description: |-
toolset for short variant discovery in genetic sequence data (examples)
vt is a variant tool set that discovers short variants from Next Generation
Sequencing data.
.
Vt-normalize is a tool to normalize representation of genetic variants in
the VCF. Variant normalization is formally defined as the consistent
representation of genetic variants in an unambiguous and concise way. In
vt a simple general algorithm to enforce this is implemented.
.
This package contains some example data.
Enhances: vt
Homepage: https://genome.sph.umich.edu/wiki/Vt
Installed-Size: '17972'
Maintainer: Debian Med Packaging Team <debian-med-packaging@lists.alioth.debian.org>
Package: vt-examples
Priority: optional
Section: science
Source: vt
Version: 0.57721+ds-3
srcpkg_name: vt
srcpkg_version: 0.57721+ds-3