Source: python-geneimpacts
Section: science
Priority: optional
Maintainer: Debian Med Packaging Team <debian-med-packaging@lists.alioth.debian.org>
Uploaders: Steffen Moeller <moeller@debian.org>
Build-Depends: debhelper (>= 11), dh-python, python3-all, python3-setuptools
Standards-Version: 4.3.0
Homepage: https://github.com/brentp/geneimpacts
Vcs-Browser: https://salsa.debian.org/med-team/geneimpacts
Vcs-Git: https://salsa.debian.org/med-team/geneimpacts.git
#Testsuite: autopkgtest-pkg-python

Package: python3-geneimpacts
Architecture: all
Depends: ${python3:Depends}, ${misc:Depends}
Recommends: snpeff, bcftools
Description: wraps command line tools to assess variants in gene sequences
 Interpersonal differences in our DNA is responsible for variations in
 our response to external stimuli, the efficiency of our metabolism or
 may even cause what is referenced as a genetic disorder.
 .
 A range of tools have been created to predict the importance of
 differences (polymorphisms) in genetic sequences at single nucleotides,
 SNPs.  This python class wraps and represents findings provided by any
 of the tools snpEff, VEP and BCFT.
