vcfnosnps

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

Install

All systems
curl cmd.cat/vcfnosnps.sh
Debian Debian
apt-get install libvcflib-tools
Ubuntu
apt-get install libvcflib-tools
image/svg+xml Kali Linux
apt-get install libvcflib-tools
Windows (WSL2)
sudo apt-get update sudo apt-get install libvcflib-tools
Dockerfile
dockerfile.run/vcfnosnps

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.