Ubuntu
plink1.9 package

plink1.9 1.90~b3.31-160203-1 source package in Ubuntu

Changelog

plink1.9 (1.90~b3.31-160203-1) unstable; urgency=low

  * New upstream release (Closes: #811910)
  * debian/control:
     - Standards-Version: 3.9.7 (no changes needed)
     - Fixed lintian vcs-field-uses-insecure-uri

 -- Dylan Aïssi <email address hidden>  Thu, 04 Feb 2016 22:12:20 +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:
Low Urgency

See full publishing history Publishing

Series Pocket Published Component Section
Xenial release universe misc

Downloads

File Size SHA-256 Checksum
plink1.9_1.90~b3.31-160203-1.dsc 2.1 KiB 401772b53954e72b6e3bf315b32cd146196c2bd544b8d313d8b8fed7ab35152f
plink1.9_1.90~b3.31-160203.orig.tar.xz 703.7 KiB 9a42a12f004a32b76b9e563b4abcae408c6cccd71be38409c27bc31daae231af
plink1.9_1.90~b3.31-160203-1.debian.tar.xz 8.3 KiB a24e55ed3b2140fb21fc7882fbfcaa0bad63661098a0223be0a0d3ea48dcdcbf

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/README.Debian.

plink1.9-dbgsym: debug symbols for package plink1.9

 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/README.Debian.