Source: plink
Section: science
Priority: optional
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>
Build-Depends: debhelper (>= 9), zlib1g-dev
Standards-Version: 3.9.3
Vcs-Browser: http://svn.debian.org/wsvn/debian-med/trunk/packages/plink/trunk/
Vcs-Svn: svn://svn.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}
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 p-link
 because of a name clash.  Please read more about this
 in /usr/share/doc/README.Debian.
