Source: nanosv
Standards-Version: 4.7.4
Maintainer: Debian Med Packaging Team <debian-med-packaging@lists.alioth.debian.org>
Uploaders:
 Steffen Moeller <moeller@debian.org>,
Section: science
Build-Depends:
 debhelper-compat (= 14),
 dh-sequence-python3,
 help2man,
 python3-all,
 python3-setuptools,
 python3-vcf,
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

Package: nanosv
Architecture: all
Depends:
 python3-pysam,
 python3-vcf,
 ${misc:Depends},
 ${python3:Depends},
Recommends:
 sambamba,
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.
