URL: https://github.com/NCI-CGR/PLP_prediction_workflow/tree/autogvp
Proper Citation: AutoGVP (RRID:SCR_026107)
Description: Software tool integrates ClinVar variant annotation with modified InterVar classification approach, based on American College of Medical Genetics-Association for Molecular Pathology guidelines, to output germline variant classification. Since AutoGVP input only requires VCF file, it can facilitate large-scale, clinically focused classification of germline sequence variants.
Synonyms: Automated Germline Variant Pathogenicity
Resource Type: software resource, software application, source code
Defining Citation: PMID:38426335
Keywords: germline variant classification, germline sequence variants, germline, sequence variants,
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