plink1.9 1.90~b4.7-170906-1 source package in Ubuntu
Changelog
plink1.9 (1.90~b4.7-170906-1) unstable; urgency=medium * New upstream release. * Add references to registries. * Update 01.Fix_Makefile.patch. * Bump Standards-Version to 4.1.0. * Remove Testsuite field from d/control, now automatically added. * cme fix dpkg-control. -- Dylan Aïssi <email address hidden> Fri, 15 Sep 2017 23:53:58 +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 |
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Downloads
File | Size | SHA-256 Checksum |
---|---|---|
plink1.9_1.90~b4.7-170906-1.dsc | 2.1 KiB | 764fc4b92f45aa04054d0e0d5453fed46ed5c796a7b54f0138f980062c862f24 |
plink1.9_1.90~b4.7-170906.orig.tar.xz | 714.1 KiB | 04ff00766deb764f7507aafc4883921856204337c17502de54188cb2c0affd93 |
plink1.9_1.90~b4.7-170906-1.debian.tar.xz | 18.6 KiB | f824f6a1ad96cfa047e7ae47c55297f955e930c7534acd7dfbaf0f76c394796d |
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