libvcflib 1.0.9+dfsg1-3 source package in Ubuntu
Changelog
libvcflib (1.0.9+dfsg1-3) unstable; urgency=medium
* add support for loong64 arch
Closes: #1057253
-- Andreas Tille <email address hidden> Sun, 03 Dec 2023 13:29:41 +0100
Upload details
- Uploaded by:
- Debian Med
- Uploaded to:
- Sid
- Original maintainer:
- Debian Med
- Architectures:
- any-amd64 arm64 loong64 mips64el ppc64el s390x ia64 ppc64 riscv64 sparc64 alpha
- Section:
- misc
- Urgency:
- Medium Urgency
See full publishing history Publishing
| Series | Published | Component | Section |
|---|
Downloads
| File | Size | SHA-256 Checksum |
|---|---|---|
| libvcflib_1.0.9+dfsg1-3.dsc | 2.6 KiB | cf8c7059dd4409d8210edb9554f6dfd0089b254d91cc9e205e14ef8a9267e3d3 |
| libvcflib_1.0.9+dfsg1.orig.tar.xz | 8.6 MiB | 3d0f48f9157a9f9b896143b6789f52f12898cb8e1438a4ad50d4ef27477f300f |
| libvcflib_1.0.9+dfsg1-3.debian.tar.xz | 72.5 KiB | 6bfa8f11e3054e5e67a929769884daba8581e1ffbd5954a3aa2301b4254f4a71 |
Available diffs
- diff from 1.0.9+dfsg1-2 to 1.0.9+dfsg1-3 (536 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
- libvcflib2: 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.
- libvcflib2-dbgsym: debug symbols for libvcflib2
