deb_control_files:
- control
- md5sums
deb_fields:
Architecture: amd64
Depends: libc6 (>= 2.38), libdisorder0 (>= 0.0.2), libfastahack0 (>= 0.0+git20160702.bbc645f),
libgcc-s1 (>= 3.3.1), libgomp1 (>= 4.2.1), libsmithwaterman0 (>= 0.0+git20160702.2610e25),
libstdc++6 (>= 13.1), libtabixpp0t64 (>= 1.0.0), libvcflib2 (>= 1.0.9+dfsg1),
libwfa2-0 (>= 2.3.3), python3:any, r-base-core, r-cran-plyr, r-cran-ggplot2, r-cran-gridbase
Description: |-
C++ library for parsing and manipulating VCF files (tools)
The Variant Call Format (VCF) is a flat-file, tab-delimited textual format
intended to concisely describe reference-indexed variations between
individuals. VCF provides a common interchange format for the description of
variation in individuals and populations of samples, and has become the defacto
standard reporting format for a wide array of genomic variant detectors.
.
vcflib provides methods to manipulate and interpret sequence variation as it
can be described by VCF. It is both:
.
* an API for parsing and operating on records of genomic variation as it can
be described by the VCF format,
* and a collection of command-line utilities for executing complex
manipulations on VCF files.
.
This package contains several tools using the library.
Homepage: https://github.com/vcflib/vcflib
Installed-Size: '3846'
Maintainer: Debian Med Packaging Team <debian-med-packaging@lists.alioth.debian.org>
Package: libvcflib-tools
Priority: optional
Section: science
Source: libvcflib (1.0.9+dfsg1-3)
Suggests: r-cran-pracma
Version: 1.0.9+dfsg1-3+b2
srcpkg_name: libvcflib
srcpkg_version: 1.0.9+dfsg1-3