[ 源代码： plink ]
软件包：plink（1.07+dfsg-3）
plink 的相关链接
Debian 的资源：
下载源码包 plink：
维护小组：
- Debian Med Packaging Team (QA 页面, 邮件存档)
- Steffen Moeller (QA 页面)
- Andreas Tille (QA 页面)
- Charles Plessy (QA 页面)
- Dylan Aïssi (QA 页面)
外部的资源：
- 主页 [zzz.bwh.harvard.edu]
相似软件包：
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/plink/README.Debian.
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