libvcflib 1.0.2+dfsg-4 source package in Ubuntu
Changelog
libvcflib (1.0.2+dfsg-4) unstable; urgency=medium
* Install scripts
Closes: #989014
-- Andreas Tille <email address hidden> Fri, 24 Dec 2021 10:51:57 +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_1.0.2+dfsg-4.dsc | 2.2 KiB | 5a0b81820587ee801e5a469fd7d013fca085a9f10a1729ae7d957779b668f722 |
| libvcflib_1.0.2+dfsg.orig.tar.xz | 7.2 MiB | 922bcb38ce670de70b7d95a261bab6f711f0fd0ee3d5f5465316664af656d125 |
| libvcflib_1.0.2+dfsg-4.debian.tar.xz | 9.2 KiB | ecdd240027bea1906cea7b28de2d072b8cb6a37bbef3c752ed8bca3be66f6e58 |
Available diffs
- diff from 1.0.2+dfsg-3 to 1.0.2+dfsg-4 (654 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
