deb_control_files:
- control
- md5sums
deb_fields:
Architecture: all
Depends: python3:any, bsdextrautils | bsdmainutils (<< 12.1.1~)
Description: |-
optional scripts and example resources for mindthegap
Designed to call insertions of any size, whether they are novel or
duplicated, homozygous or heterozygous in the donor genome. it takes
as input a set of reads and a reference genome. It outputs two sets
of FASTA sequences: one is the set of breakpoints of detection
insertion sites, the other is the set of assembled insertions for
each breakpoint. MindTheGap can also be used as a genome assembly
finishing tool. It can fill the gap between a set of input contigs
without any a priori on their relative order and orientation. It
outputs the results in gfa file. Please note that this package is
meant to accommodate the mindthegap package and only acts as example
to how this package can be utilised.
Homepage: https://github.com/GATB/MindTheGap
Installed-Size: '730'
Maintainer: Debian Med Packaging Team <debian-med-packaging@lists.alioth.debian.org>
Package: mindthegap-examples
Priority: optional
Recommends: mindthegap
Section: science
Source: mindthegap
Version: 2.3.0-2
srcpkg_name: mindthegap
srcpkg_version: 2.3.0-2