libvcflib 1.0.0~rc1+dfsg1-3ubuntu1 source package in Ubuntu

Changelog

libvcflib (1.0.0~rc1+dfsg1-3ubuntu1) zesty; urgency=medium

  * Revert 'Adapt to recent PIE changes in dpkg' as they have
    not happened in Ubuntu yet

 -- Graham Inggs <email address hidden>  Thu, 09 Mar 2017 13:07:46 +0200

Upload details

Uploaded by:
Graham Inggs on 2017-03-09
Uploaded to:
Zesty
Original maintainer:
Ubuntu Developers
Architectures:
any
Section:
misc
Urgency:
Medium Urgency

See full publishing history Publishing

Series Pocket Published Component Section
Zesty release on 2017-03-09 universe misc

Downloads

File Size SHA-256 Checksum
libvcflib_1.0.0~rc1+dfsg1.orig.tar.xz 6.3 MiB 47bc7a7212f0f2db4a48a080b3affdb0187212ef73f397b4368ef76e55f834c5
libvcflib_1.0.0~rc1+dfsg1-3ubuntu1.debian.tar.xz 10.4 KiB d3636d06b0623ce4ca0c33b9049eb93a51c60a01ea92d74c67c69a385f2c4391
libvcflib_1.0.0~rc1+dfsg1-3ubuntu1.dsc 2.3 KiB 07454cb057306298fbeb06ead3453403e059d04760c5aa7dc3bee2fc26df8d25

View changes file

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.

libvcflib1: 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.

libvcflib1-dbgsym: Debug symbols for libvcflib1