Source: plink2
Maintainer: Debian Med Packaging Team <debian-med-packaging@lists.alioth.debian.org>
Uploaders: Dylan Aïssi <daissi@debian.org>
Section: science
Priority: optional
Build-Depends: debhelper-compat (= 13),
               help2man,
               liblapack-dev | liblapack.so,
               libzstd-dev,
               zlib1g-dev,
               libsimde-dev,
               libdeflate-dev
Standards-Version: 4.6.2
Vcs-Browser: https://salsa.debian.org/med-team/plink2
Vcs-Git: https://salsa.debian.org/med-team/plink2.git
Homepage: https://www.cog-genomics.org/plink/2.0/
Rules-Requires-Root: no

Package: plink2
Architecture: any
Depends: ${misc:Depends},
         ${shlibs:Depends}
Built-Using: ${simde:Built-Using}
Description: whole-genome association analysis toolset
 plink expects as input the data from SNP (single nucleotide polymorphism)
 chips of many individuals and their phenotypical description of a disease.
 It finds associations of single or pairs of DNA variations with a phenotype
 and can retrieve SNP annotation from an online source.
 .
 SNPs can evaluated individually or as pairs for their association with the
 disease phenotypes. The joint investigation of copy number variations is
 supported. A variety of statistical tests have been implemented.
 .
 plink2 is a comprehensive update of plink and plink1.9 with new algorithms
 and new methods, faster and less memory consumer than the first plink.