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

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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 Pocket 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

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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