cnvkit 0.9.9-2 source package in Ubuntu
Changelog
cnvkit (0.9.9-2) unstable; urgency=medium * Team Upload. * Re-diff patches (refresh) * d/rules: do not run tests in parallel -- Nilesh Patra <email address hidden> Fri, 15 Oct 2021 12:11:06 +0530
Upload details
- Uploaded by:
- Debian Med
- Uploaded to:
- Sid
- Original maintainer:
- Debian Med
- Architectures:
- amd64 arm64 ppc64el
- Section:
- misc
- Urgency:
- Medium Urgency
See full publishing history Publishing
Series | Published | Component | Section | |
---|---|---|---|---|
Mantic | release | universe | misc | |
Lunar | release | universe | misc | |
Jammy | release | universe | misc |
Downloads
File | Size | SHA-256 Checksum |
---|---|---|
cnvkit_0.9.9-2.dsc | 2.3 KiB | 9762ab0c3f49c481a8d19713e6684553a989b9677489ae2c31c97f2ecdb783b6 |
cnvkit_0.9.9.orig.tar.gz | 22.6 MiB | 8c8c94d0f2736bf98c32853926dbcdb93633c21a05c737f0920d714a5a07b054 |
cnvkit_0.9.9-2.debian.tar.xz | 6.1 KiB | fa40ad3bf5ae8abaea931958c1b4dca6170c3e6cd8f8747dd61cebbc74f55c7b |
Available diffs
- diff from 0.9.8-1 to 0.9.9-2 (11.0 KiB)
No changes file available.
Binary packages built by this source
- cnvkit: Copy number variant detection from targeted DNA sequencing
A command-line toolkit and Python library for detecting copy number variants
and alterations genome-wide from targeted DNA sequencing. It is designed for
use with hybrid capture, including both whole-exome and custom target panels,
and short-read sequencing platforms such as Illumina and Ion Torrent.