libvcflib 1.0.0~rc2+dfsg-2 source package in Ubuntu

Changelog

libvcflib (1.0.0~rc2+dfsg-2) unstable; urgency=medium

  * Add libfastahack to pkg-config input file
  * Depends: libfastahack-dev

 -- Andreas Tille <email address hidden>  Fri, 14 Sep 2018 13:56:52 +0200

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Uploaded by:
Debian Med on 2018-09-14
Uploaded to:
Sid
Original maintainer:
Debian Med
Architectures:
any
Section:
misc
Urgency:
Medium Urgency

See full publishing history Publishing

Series Pocket Published Component Section
Eoan release on 2019-04-18 universe misc
Disco release on 2018-11-09 universe misc

Downloads

File Size SHA-256 Checksum
libvcflib_1.0.0~rc2+dfsg-2.dsc 2.3 KiB 6fe7185f4ea36315a03addf60c66df3cd94374b0fef07bfdb8dbb49ffd6c13a7
libvcflib_1.0.0~rc2+dfsg.orig.tar.xz 7.8 MiB 398525ae81de73eb96f636c1d95db9b3fe609ad2ef714a6720e42940885324d4
libvcflib_1.0.0~rc2+dfsg-2.debian.tar.xz 11.5 KiB b40163d79e75ed6a42e1e2fcffe8ba457201510f8801b3f674a98c01f098661e

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: 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