libvcflib 1.0.9+dfsg1-2 source package in Ubuntu

Changelog

libvcflib (1.0.9+dfsg1-2) unstable; urgency=medium

  * Source-only upload.

 -- Andreas Tille <email address hidden>  Sun, 06 Aug 2023 23:01:54 +0200

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 Pocket Published Component Section
Mantic release universe misc

Downloads

File Size SHA-256 Checksum
libvcflib_1.0.9+dfsg1-2.dsc 2.6 KiB 3a3a66789ca945e019f525c45d7cb8cbd4bac147ce878751a4fb2e3816a5680c
libvcflib_1.0.9+dfsg1.orig.tar.xz 8.6 MiB 3d0f48f9157a9f9b896143b6789f52f12898cb8e1438a4ad50d4ef27477f300f
libvcflib_1.0.9+dfsg1-2.debian.tar.xz 72.5 KiB c950eeff63a7b85b3ceecce0b10660f0cb403d35f7a6c9cca97d0db34de0ff4b

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