libvcflib 1.0.9+dfsg1-3build1 source package in Ubuntu
Changelog
libvcflib (1.0.9+dfsg1-3build1) noble; urgency=medium * No-change rebuild against libtabixpp0t64. -- Colin Watson <email address hidden> Sun, 14 Apr 2024 19:01:17 +0100
Upload details
- Uploaded by:
- Colin Watson
- Uploaded to:
- Noble
- 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 | |
---|---|---|---|---|
Oracular | release | universe | misc | |
Noble | release | universe | misc |
Downloads
File | Size | SHA-256 Checksum |
---|---|---|
libvcflib_1.0.9+dfsg1.orig.tar.xz | 8.6 MiB | 3d0f48f9157a9f9b896143b6789f52f12898cb8e1438a4ad50d4ef27477f300f |
libvcflib_1.0.9+dfsg1-3build1.debian.tar.xz | 72.5 KiB | 632aa6687fde15a603c889d856a3bde6862d0bf4f4273f7035defdfa286d51a5 |
libvcflib_1.0.9+dfsg1-3build1.dsc | 2.6 KiB | 0973ada45b0de21549c15d6f05d081cc91842de61fc355e15694332f89505756 |
Available diffs
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