plink1.9 1.90~b6.26-220402-1 source package in Ubuntu
Changelog
plink1.9 (1.90~b6.26-220402-1) unstable; urgency=medium * New upstream release. * Standards-Version: 4.6.1 (no changes needed) -- Dylan Aïssi <email address hidden> Fri, 29 Jul 2022 16:23:52 +0200
Upload details
- Uploaded by:
- Debian Med
- Uploaded to:
- Sid
- Original maintainer:
- Debian Med
- Architectures:
- any-amd64 any-i386 armel armhf mipsel
- 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 |
---|---|---|
plink1.9_1.90~b6.26-220402-1.dsc | 2.1 KiB | 4f31340d35e5ddf7c5f5c8b935b1c2bca9e35a3f96f7c71462194c118cadfcd4 |
plink1.9_1.90~b6.26-220402.orig.tar.xz | 719.9 KiB | 21d0f56134965f6904336ddf8d61dc27b834dab97a064d8bee2b909185993e59 |
plink1.9_1.90~b6.26-220402-1.debian.tar.xz | 45.8 KiB | c838ca150d1a9fcd25af1d0b9713cf6ce9d5b757662d888680c76b3e9eec7add |
Available diffs
No changes file available.
Binary packages built by this source
- plink1.9: 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.
.
plink1.9 is a comprehensive update of plink with new algorithms and new
methods, faster and less memory consumer than the first plink.
.
Please note: The executable was renamed to plink1.9
because of a name clash. Please read more about this
in /usr/share/doc/plink1. 9/README. Debian.
- plink1.9-dbgsym: debug symbols for plink1.9