r-bioc-purecn 2.0.1+dfsg-1 source package in Ubuntu
Changelog
r-bioc-purecn (2.0.1+dfsg-1) unstable; urgency=medium * Allow failure for piuparts * New upstream version * dh-update-R to update Build-Depends (routine-update) -- Andreas Tille <email address hidden> Fri, 26 Nov 2021 14:11:47 +0100
Upload details
- Uploaded by:
- Debian R Packages Maintainers
- Uploaded to:
- Sid
- Original maintainer:
- Debian R Packages Maintainers
- Architectures:
- all
- Section:
- misc
- Urgency:
- Medium Urgency
See full publishing history Publishing
Series | Published | Component | Section | |
---|---|---|---|---|
Jammy | release | universe | misc |
Downloads
File | Size | SHA-256 Checksum |
---|---|---|
r-bioc-purecn_2.0.1+dfsg-1.dsc | 2.4 KiB | a569546f48c949a8d9303f533dec74af28f4a30bd79fa2735c8d2e8d242bef08 |
r-bioc-purecn_2.0.1+dfsg.orig.tar.xz | 4.7 MiB | 351b978f01ba06c42c243f946030f7324df39ccbbdf596d48df06fa0c015d05c |
r-bioc-purecn_2.0.1+dfsg-1.debian.tar.xz | 6.0 KiB | 5626746d5cef95262ef406fff2f6555a357f0d84289eaec61494dc139a813d61 |
Available diffs
- diff from 1.22.2+dfsg-1 to 2.0.1+dfsg-1 (115.1 KiB)
No changes file available.
Binary packages built by this source
- r-bioc-purecn: copy number calling and SNV classification using targeted short read sequencing
This package estimates tumor purity, copy number, and loss of
heterozygosity (LOH), and classifies single nucleotide variants (SNVs) by
somatic status and clonality. PureCN is designed for targeted short read
sequencing data, integrates well with standard somatic variant detection
and copy number pipelines, and has support for tumor samples without
matching normal samples.