vcfsitesummarize

Vcfsitesummarize Command

Vcfsitesummarize Command

vcfsitesummarize

C++ library for parsing and manipulating VCF files (tools)

Maintainer: Debian Med Packaging Team



Section: science

Install vcfsitesummarize

  • Debian apt-get install libvcflib-tools Click to copy
  • Ubuntu apt-get install libvcflib-tools Click to copy
  • Kali Linux apt-get install libvcflib-tools Click to copy

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.

Installing vcfsitesummarize command is simple. just copy one of the above commands for your operating system and paste it into terminal. This command is available for Debian, Ubuntu and Kali operating systems. Once you run the command it will install the latest version of vcfsitesummarize 2023 package in your OS.