cnvkit 0.9.10-1 source package in Ubuntu
Changelog
cnvkit (0.9.10-1) unstable; urgency=medium
* Team upload.
[ Andreas Tille ]
* New upstream version
* Standards-Version: 4.6.2 (routine-update)
* Drop Build-Depends python3-future
Closes: #1059947
* Build-Depends: s/dh-python/dh-sequence-python3/ (routine-update)
* Use secure URI in Homepage field.
[ Nilesh Patra ]
* Add patch to ignore test warnings
-- Andreas Tille <email address hidden> Fri, 05 Jan 2024 16:18:13 +0100
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 | |
|---|---|---|---|---|
| Noble | release | universe | misc |
Downloads
| File | Size | SHA-256 Checksum |
|---|---|---|
| cnvkit_0.9.10-1.dsc | 2.4 KiB | 6b652f5a9e9a519a17fdbed744ac658895417cb2ceb3580f448c1095f6c3cf7f |
| cnvkit_0.9.10.orig.tar.gz | 22.6 MiB | 56739496f1f59511661107e662d81e5fd8af413571e853b0a1b34d882a19349a |
| cnvkit_0.9.10-1.debian.tar.xz | 17.0 KiB | ac6661114a6424a4413134531fe6a3a0222f536eb22eba44cac010f7141d09ff |
Available diffs
- diff from 0.9.9-2 to 0.9.10-1 (191.1 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.
