libvcflib 1.0.3+dfsg-2 source package in Ubuntu
Changelog
libvcflib (1.0.3+dfsg-2) unstable; urgency=medium * Fix watch file * Standards-Version: 4.6.1 (routine-update) -- Andreas Tille <email address hidden> Fri, 07 Oct 2022 16:26:06 +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 | |
|---|---|---|---|---|
| Lunar | release | universe | misc |
Downloads
| File | Size | SHA-256 Checksum |
|---|---|---|
| libvcflib_1.0.3+dfsg-2.dsc | 2.2 KiB | 603d62ca7b7558ed66caf394a149695db26a8a8264a83f7333c0f9a93e75f4e7 |
| libvcflib_1.0.3+dfsg.orig.tar.xz | 7.2 MiB | 34f4692321cbbfc7fa5761f8d61ec50dd44bafa3dc23a6dad82772114e551ddc |
| libvcflib_1.0.3+dfsg-2.debian.tar.xz | 7.9 KiB | 90f2687a06bcba4f158d64dccb01d849a532707204f283f23ef9b3cad8d09bac |
Available diffs
- diff from 1.0.3+dfsg-1 to 1.0.3+dfsg-2 (631 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: No summary available for libvcflib1 in ubuntu mantic.
No description available for libvcflib1 in ubuntu mantic.
- libvcflib1-dbgsym: debug symbols for libvcflib1
