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Source: plink1.9
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 (>= 11~),
help2man,
libatlas-base-dev,
liblapack-dev,
zlib1g-dev
Standards-Version: 4.2.1
Vcs-Browser: https://salsa.debian.org/med-team/plink1-9
Vcs-Git: https://salsa.debian.org/med-team/plink1-9.git
Homepage: https://www.cog-genomics.org/plink/1.9/
Package: plink1.9
Architecture: any-amd64 any-i386 armel armhf mipsel
Depends: ${misc:Depends},
${shlibs:Depends}
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.
.
plink1.9 is a comprehensive update of plink with new algorithms and new
methods, faster and less memory consumer than the first plink.
.
Please note: The executable was renamed to plink1.9
because of a name clash. Please read more about this
in /usr/share/doc/plink1.9/README.Debian.
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