deb_control_files:
- control
- md5sums
- postinst
- prerm
deb_fields:
Architecture: all
Depends: python3-biopython, python3-matplotlib, python3-numpy, python3-pandas, python3-pomegranate,
python3-pyfaidx, python3-pysam, python3-reportlab, python3-scipy, python3-sklearn,
python3:any, r-bioc-dnacopy
Description: |-
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.
Homepage: https://cnvkit.readthedocs.org
Installed-Size: '94731'
Maintainer: Debian Med Packaging Team <debian-med-packaging@lists.alioth.debian.org>
Package: cnvkit
Priority: optional
Section: science
Version: 0.9.10-2
srcpkg_name: cnvkit
srcpkg_version: 0.9.10-2