plink2 2.00~a3.5-220809+dfsg-1 source package in Ubuntu
Changelog
plink2 (2.00~a3.5-220809+dfsg-1) unstable; urgency=medium * Team upload. * Fix watch file (seems we are at ~a3.5 released at 220809) -- Andreas Tille <email address hidden> Mon, 12 Dec 2022 09:35:02 +0100
Upload details
- Uploaded by:
- Debian Med
- Uploaded to:
- Sid
- Original maintainer:
- Debian Med
- Architectures:
- any
- Section:
- misc
- Urgency:
- Medium Urgency
See full publishing history Publishing
Series | Published | Component | Section | |
---|---|---|---|---|
Mantic | release | universe | misc | |
Lunar | release | universe | misc |
Downloads
File | Size | SHA-256 Checksum |
---|---|---|
plink2_2.00~a3.5-220809+dfsg-1.dsc | 2.1 KiB | 21dc883787ffdb558884c873ad5f63e3b5a790a0eb4a2a94c3e23804d73939b8 |
plink2_2.00~a3.5-220809+dfsg.orig.tar.xz | 940.2 KiB | af8ec65e5c0e9e74fc5a26ab5318f6a8a4c9350559bc9fd009499d7fc2cfdc1a |
plink2_2.00~a3.5-220809+dfsg-1.debian.tar.xz | 50.9 KiB | 81ca7bb42672e0f71270289a744ea0fd6db795a7a830764454fd06f507f05147 |
Available diffs
No changes file available.
Binary packages built by this source
- plink2: 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.
.
plink2 is a comprehensive update of plink and plink1.9 with new algorithms
and new methods, faster and less memory consumer than the first plink.
- plink2-dbgsym: debug symbols for plink2