libvcflib 1.0.9+dfsg1-1 source package in Ubuntu

Changelog

libvcflib (1.0.9+dfsg1-1) unstable; urgency=medium

  * Bump SOVERSION due to ABI change
    Closes: #1032557
  * Attempt to use d-shlibs delayed for later once shared and static lib
    are created both
  * Drop unneeded header files with questionable licenses

 -- Andreas Tille <email address hidden>  Sun, 23 Jul 2023 10:42:25 +0200

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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

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File Size SHA-256 Checksum
libvcflib_1.0.9+dfsg1-1.dsc 2.6 KiB 93bc6ffaae0352a93d17f4822e25dd322577e154fd84f6601ca357a54e9e6028
libvcflib_1.0.9+dfsg1.orig.tar.xz 8.6 MiB 3d0f48f9157a9f9b896143b6789f52f12898cb8e1438a4ad50d4ef27477f300f
libvcflib_1.0.9+dfsg1-1.debian.tar.xz 72.5 KiB dc3dd80324af7c0b9db44860e76db8c65a744ada1ce091a86da5b8a3ba96c06f

Available diffs

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