May 26, 2018
C++ library and CLI tools 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.
The API itself provides a quick and extremely permissive method to read and write VCF files. Extensions and applications of the library provided in the included utilities *.cpp comprise the vast bulk of the library’s utility for most users.