libvcflib 1.0.9+dfsg-1 source package in Ubuntu

Changelog

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

  [ Étienne Mollier ]
  * New upstream version 1.0.9+dfsg
  * d/patches: refresh everything.
  * wfa2_linking: add patch; fix linker errors.

  [ Andreas Tille ]
  * libvcflib-dev: Depends: libwfa2-dev
    Closes: #1031473

 -- Andreas Tille <email address hidden>  Sun, 19 Feb 2023 13:54:18 +0100

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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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Downloads

File Size SHA-256 Checksum
libvcflib_1.0.9+dfsg-1.dsc 2.6 KiB 52b0a2cb2ea9e3c44863358a19ae4f477b1371669d576f6f781f9301a5262dd6
libvcflib_1.0.9+dfsg.orig.tar.xz 8.6 MiB d802000860b786a021ca55e8f6bf15ca5e042c10e291e8bcc0c956f5794f53bf
libvcflib_1.0.9+dfsg-1.debian.tar.xz 72.1 KiB a75756329ca52af613b6dce4b33694975be3be5e9e4521923fbd7f33ebd44db9

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
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: No summary available for libvcflib1-dbgsym in ubuntu mantic.

No description available for libvcflib1-dbgsym in ubuntu mantic.