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Source: nanosv
Maintainer: Debian Med Packaging Team <debian-med-packaging@lists.alioth.debian.org>
Uploaders: Steffen Moeller <moeller@debian.org>
Section: science
Priority: optional
Build-Depends: debhelper-compat (= 13),
dh-sequence-python3,
help2man,
python3-all,
python3-setuptools,
python3-vcf
Standards-Version: 4.7.0
Vcs-Browser: https://salsa.debian.org/med-team/nanosv
Vcs-Git: https://salsa.debian.org/med-team/nanosv.git
Homepage: https://github.com/mroosmalen/nanosv
Rules-Requires-Root: no
Package: nanosv
Architecture: all
Recommends: sambamba
Depends: python3-pysam, python3-vcf, ${misc:Depends}, ${python3:Depends}
Description: structural variant caller for nanopore data
NanoSV is a software package that can be used to identify structural
genomic variations in long-read sequencing data, such as data produced
by Oxford Nanopore Technologies’ MinION, GridION or PromethION
instruments, or Pacific Biosciences RSII or Sequel sequencers. NanoSV
has been extensively tested using Oxford Nanopore MinION sequencing data.
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