plink 1.07-1 (armhf binary) in ubuntu precise
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/
Details
- Package version:
- 1.07-1
- Status:
- Published
- Component:
- universe
- Priority:
- Optional
Downloadable files
armhf build of plink 1.07-1 in ubuntu precise RELEASE produced
these files:
- plink_1.07-1_armhf.deb (1.1 MiB)