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URL: https://github.com/ekg/vcflib
Proper Citation: vcflib (RRID:SCR_001231)
Description: A C++ library for parsing and manipulating Variant Call Format (VCF) files, and many command-line utilities. The API 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.
Abbreviations: vcflib
Resource Type: software library, software resource, software toolkit
Keywords: c++, sequence variation, genomic variation, bio.tools
Availability: Free, Available for download, Freely available
Resource Name: vcflib
Resource ID: SCR_001231
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Source: SciCrunch Registry (RRID:SCR_005400)
Description: Interactive portal for finding and submitting biomedical resources. Resources within SciCrunch have assigned RRIDs which are used to cite resources in scientific manuscripts. SciCrunch Registry, formerly NIF Registry, provides resources catalog. Allows to add new resources. Allows edit existing resources after registration. Curators are tasked with identifying and registering resources, examining data, writing configuration files to index and display data and keeping contents current.
URL: https://rrid.site/rin/sources/SCR_005400
