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Source: plink
Maintainer: Debian Med Packaging Team <debian-med-packaging@lists.alioth.debian.org>
Uploaders: Steffen Moeller <moeller@debian.org>,
Andreas Tille <tille@debian.org>,
Charles Plessy <plessy@debian.org>,
Dylan Aïssi <bob.dybian@gmail.com>
Section: science
Testsuite: autopkgtest
Priority: optional
Build-Depends: debhelper (>= 9),
zlib1g-dev
Standards-Version: 3.9.8
Vcs-Browser: https://anonscm.debian.org/viewvc/debian-med/trunk/packages/plink/trunk/
Vcs-Svn: svn://anonscm.debian.org/debian-med/trunk/packages/plink/trunk/
Homepage: http://pngu.mgh.harvard.edu/~purcell/plink/
Package: plink
Architecture: any
Depends: ${shlibs:Depends},
${misc:Depends}
Recommends: med-config (>= 2.1)
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.
.
Please note: The executable was renamed to plink1
because of a name clash. Please read more about this
in /usr/share/doc/README.Debian.
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