Source: plink2 Maintainer: Debian Med Packaging Team Uploaders: Dylan Aïssi Section: science Priority: optional Build-Depends: debhelper-compat (= 13), help2man, libatlas-base-dev, liblapack-dev, libzstd-dev (>= 1.4.4), zlib1g-dev, libsimde-dev, libdeflate-dev Standards-Version: 4.6.1 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.