| Literature DB >> 34428318 |
Jiguang Peng1, Jiale Xiang1,2,3, Xiangqian Jin1,4, Junhua Meng1, Nana Song1, Lisha Chen1,3, Ahmad Abou Tayoun5,6, Zhiyu Peng1,2.
Abstract
The American College of Medical Genetics and Genomics, and the Association for Molecular Pathology (ACMG/AMP) have proposed a set of evidence-based guidelines to support sequence variant interpretation. The ClinGen hearing loss expert panel (HL-EP) introduced further specifications into the ACMG/AMP framework for genetic hearing loss. This study developed a tool named Variant Interpretation Platform for genetic Hearing Loss (VIP-HL), aiming to semi-automate the HL ACMG/AMP rules. VIP-HL aggregates information from external databases to automate 13 out of 24 ACMG/AMP rules specified by HL-EP, namely PVS1, PS1, PM1, PM2, PM4, PM5, PP3, BA1, BS1, BS2, BP3, BP4, and BP7. We benchmarked VIP-HL using 50 variants in which 82 rules were activated by the ClinGen HL-EP. VIP-HL concordantly activated 93% (76/82) rules, significantly higher than that of by InterVar (48%; 39/82). VIP-HL is an integrated online tool for reliable automated variant classification in hearing loss genes. It assists curators in variant interpretation and provides a platform for users to share classifications with each other. VIP-HL is available with a user-friendly web interface at http://hearing.genetics.bgi.com/.Entities:
Keywords: bioinformatics; clinical genomics; genetic hearing loss; variant interpretation
Mesh:
Substances:
Year: 2021 PMID: 34428318 DOI: 10.1002/humu.24277
Source DB: PubMed Journal: Hum Mutat ISSN: 1059-7794 Impact factor: 4.878