libvcflib 1.0.7+dfsg-2 source package in Ubuntu
Changelog
libvcflib (1.0.7+dfsg-2) unstable; urgency=medium * Restrict architectures to 64bit only -- Andreas Tille <email address hidden> Tue, 07 Feb 2023 21:10:50 +0100
Upload details
- Uploaded by:
- Debian Med
- Uploaded to:
- Sid
- Original maintainer:
- Debian Med
- Architectures:
- any-amd64 arm64 mips64el ppc64el s390x ia64 ppc64 riscv64 sparc64 alpha
- Section:
- misc
- Urgency:
- Medium Urgency
See full publishing history Publishing
Series | Published | Component | Section |
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Downloads
File | Size | SHA-256 Checksum |
---|---|---|
libvcflib_1.0.7+dfsg-2.dsc | 2.6 KiB | e636d18455b67bca3fde794b42c62e24199f280f323467859d48d86519d61aee |
libvcflib_1.0.7+dfsg.orig.tar.xz | 8.6 MiB | 5c4b5c3f132e2f3b8b1816ce8d1dd8063a289642cec3bb905e6fa2b10b431016 |
libvcflib_1.0.7+dfsg-2.debian.tar.xz | 71.9 KiB | 12b2faaa9abfbd208582cc5e483fa6e91665e2993961b2c6e88c2d6e88c60bec |
Available diffs
- diff from 1.0.7+dfsg-1 to 1.0.7+dfsg-2 (717 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