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Source: cnvkit
Maintainer: Debian Med Packaging Team <debian-med-packaging@lists.alioth.debian.org>
Uploaders: Michael R. Crusoe <crusoe@debian.org>,
Steffen Moeller <moeller@debian.org>,
Olivier Sallou <osallou@debian.org>
Section: science
Priority: optional
Build-Depends: debhelper-compat (= 13),
dh-python,
python3-all,
python3-setuptools,
python3-pyfaidx,
help2man,
python3-biopython,
python3-pandas,
python3-numpy,
python3-pysam,
python3-scipy,
python3-matplotlib,
python3-pyvcf,
python3-future,
python3-pomegranate,
r-bioc-dnacopy,
# testing
# poppler-utils provides pdfunite, needed for the tests
poppler-utils <!nocheck>
Standards-Version: 4.5.1
Vcs-Browser: https://salsa.debian.org/med-team/cnvkit
Vcs-Git: https://salsa.debian.org/med-team/cnvkit.git
Homepage: http://cnvkit.readthedocs.org
Rules-Requires-Root: no
Package: cnvkit
Architecture: amd64 arm64 ppc64el
Depends: ${python3:Depends},
${misc:Depends},
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.
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