plink1.9 1.90~b6.12-191028-1 source package in Ubuntu
Changelog
plink1.9 (1.90~b6.12-191028-1) unstable; urgency=medium * New upstream release. * Replace ADTTMP with AUTOPKGTEST_TMP. * Switch to debhelper-compat. -- Dylan Aïssi <email address hidden> Wed, 20 Nov 2019 07:20:09 +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~b6.12-191028-1.dsc | 2.1 KiB | e7b1f927210b2fca2c02dbb81117d0231ea9a983a40d29f5b0b000a555ec5525 |
plink1.9_1.90~b6.12-191028.orig.tar.xz | 716.1 KiB | 6fd34f3a953b62d87a8957ca2019dd442c6593ff4d17daf5cd358d862651f1bd |
plink1.9_1.90~b6.12-191028-1.debian.tar.xz | 19.8 KiB | ab0cd59033189b842dffc6d789a3a409c80a2b3b8d5707c452d6ec9a2e1ff737 |
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