libvcflib 1.0.1+dfsg-2 source package in Ubuntu
Changelog
libvcflib (1.0.1+dfsg-2) unstable; urgency=medium
* Team upload.
* -tools: add ${perl:Depends}
* libvcflib{1,-dev}: add Multi-Arch: same
* Standards-Version: 4.4.1
-- Michael R. Crusoe <email address hidden> Thu, 26 Dec 2019 15:54:27 +0100
Upload details
- Uploaded by:
- Debian Med
- Uploaded to:
- Sid
- Original maintainer:
- Debian Med
- Architectures:
- any
- Section:
- misc
- Urgency:
- Medium Urgency
See full publishing history Publishing
| Series | Published | Component | Section |
|---|
Downloads
| File | Size | SHA-256 Checksum |
|---|---|---|
| libvcflib_1.0.1+dfsg-2.dsc | 2.3 KiB | ef959ad921905afabe6b28529f1d332c71fac7621f974f6860669681cf52964b |
| libvcflib_1.0.1+dfsg.orig.tar.xz | 7.2 MiB | e3e8e28bda9d04a7d489f51cd52433043b7cb954939e2d969624c0ea67e35b81 |
| libvcflib_1.0.1+dfsg-2.debian.tar.xz | 12.1 KiB | 2f9461bab9ba8cf6c427dd39044e699ff12e6a71d6d6bbfb72f693e7c101f956 |
Available diffs
- diff from 1.0.1+dfsg-1 to 1.0.1+dfsg-2 (747 bytes)
No changes file available.
Binary packages built by this source
- libvcflib-dev: C++ library for parsing and manipulating VCF files (development)
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 the static library and the header files.
- libvcflib-tools: 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.
- libvcflib-tools-dbgsym: debug symbols for libvcflib-tools
- libvcflib1: C++ library for parsing and manipulating VCF files
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.
- libvcflib1-dbgsym: debug symbols for libvcflib1
