libvcflib 1.0.2+dfsg-3 source package in Ubuntu
Changelog
libvcflib (1.0.2+dfsg-3) unstable; urgency=medium
* Fix build with gcc-11
Closes: #984139
* Standards-Version: 4.6.0 (routine-update)
-- Andreas Tille <email address hidden> Wed, 20 Oct 2021 18:33:54 +0200
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_1.0.2+dfsg-3.dsc | 2.2 KiB | 01b2fac52fc71e3260fd697c943a8c346ad4d01f43960f882ecba0b9d6307a35 |
| libvcflib_1.0.2+dfsg.orig.tar.xz | 7.2 MiB | 922bcb38ce670de70b7d95a261bab6f711f0fd0ee3d5f5465316664af656d125 |
| libvcflib_1.0.2+dfsg-3.debian.tar.xz | 9.1 KiB | 6f3bfe0247387891c1f5deb88bf5aa3be61028257c30270b2ae25601bbb89c20 |
Available diffs
- diff from 1.0.2+dfsg-2 to 1.0.2+dfsg-3 (1.2 KiB)
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
