plink1.9 1.90~b5-171114-1 source package in Ubuntu
Changelog
plink1.9 (1.90~b5-171114-1) unstable; urgency=medium * New upstream release. * Remove 01.Fix_Makefile.patch applied upstream. -- Dylan Aïssi <email address hidden> Thu, 30 Nov 2017 22:53:23 +0100
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 |
---|
Downloads
File | Size | SHA-256 Checksum |
---|---|---|
plink1.9_1.90~b5-171114-1.dsc | 2.1 KiB | 32f33f14d7cb0131f6de914cb94a21c71361f687cfff686f8ae88c715a1330a6 |
plink1.9_1.90~b5-171114.orig.tar.xz | 714.8 KiB | 351e9f30b561a7807ab82f8130648afc7d99eb3837dc76ae944bc789fa0c6a06 |
plink1.9_1.90~b5-171114-1.debian.tar.xz | 18.9 KiB | f3a76c00b2787f2a0fcd63f962c550273e99036bbe4412cd62bfd8947f0d3250 |
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