plink1.9 1.90~b4.9-171013-1 source package in Ubuntu
Changelog
plink1.9 (1.90~b4.9-171013-1) unstable; urgency=medium * New upstream release. * Bump Standards-Version: 4.1.1 (no changes needed). * Remove trailing whitespace characters in d/changelog. -- Dylan Aïssi <email address hidden> Fri, 03 Nov 2017 00:04:00 +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 |
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Downloads
File | Size | SHA-256 Checksum |
---|---|---|
plink1.9_1.90~b4.9-171013-1.dsc | 2.1 KiB | 10de90eb47f47ae9de2e7f0d33111f07e84a8e556860f5eac8a164673664de8a |
plink1.9_1.90~b4.9-171013.orig.tar.xz | 714.4 KiB | 8a08027fe08c4128748d0da1f9e47faf6dada3e2f4e73053ed6a4fb36ead0b20 |
plink1.9_1.90~b4.9-171013-1.debian.tar.xz | 18.9 KiB | f240081a25d92bad011502c1f4f28f48ea87f33c5fb9c96a3e1d977b43800d92 |
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