vcfnulldotslashdot

Vcfnulldotslashdot Command

Vcfnulldotslashdot Command

vcfnulldotslashdot

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

Maintainer: Debian Med Packaging Team



Section: science

Install vcfnulldotslashdot

  • 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.

Installation of latest vcfnulldotslashdot command is available for Debian, Ubuntu and Kali. You can copy the command for your OS from above and paste it into your terminal. Once you run the command it will download the 2023 latest package from the repository and install it in your computer/server.