plink1.9 1.90~b3w-150903-1 source package in Ubuntu
Changelog
plink1.9 (1.90~b3w-150903-1) unstable; urgency=low
* New upstream release
* debian/upstream/metadata: Update reference paper
* debian/control: Disable build for unsupported architectures,
thanks to Gert Wollny (Closes: #799471)
* debian/copyright: Update
-- Dylan Aïssi <email address hidden> Sat, 19 Sep 2015 15:44:10 +0200
Upload details
- Uploaded by:
- Debian Med
- Uploaded to:
- Sid
- Original maintainer:
- Debian Med
- Architectures:
- amd64 armel armhf i386 hurd-i386 kfreebsd-amd64 kfreebsd-i386 mipsel
- Section:
- misc
- Urgency:
- Low Urgency
See full publishing history Publishing
| Series | Published | Component | Section |
|---|
Downloads
| File | Size | SHA-256 Checksum |
|---|---|---|
| plink1.9_1.90~b3w-150903-1.dsc | 2.1 KiB | 0ed2558ff8951b4cfb67da882ed0aa72ac3e799f2f00d1939c0aadb1f70add49 |
| plink1.9_1.90~b3w-150903.orig.tar.gz | 1004.8 KiB | c50b939475d4938186a65601372a39832ec4b5a42709487ffb050e13063da929 |
| plink1.9_1.90~b3w-150903-1.debian.tar.xz | 8.2 KiB | 2574de700c1829f0f6b9dc146942af57a92d876c739d5ad5414aeef2e10696a1 |
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.
