Literature DB >> 34428318

VIP-HL: Semi-automated ACMG/AMP variant interpretation platform for genetic hearing loss.

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/.
© 2021 Wiley Periodicals LLC.

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


  6 in total

1.  Comprehensive interpretation of single-nucleotide substitutions in GJB2 reveals the genetic and phenotypic landscape of GJB2-related hearing loss.

Authors:  Jiale Xiang; Xiangzhong Sun; Nana Song; Sathishkumar Ramaswamy; Ahmad N Abou Tayoun; Zhiyu Peng
Journal:  Hum Genet       Date:  2022-09-01       Impact factor: 5.881

2.  Novel homozygous variant in the PDZD7 gene in a family with nonsyndromic sensorineural hearing loss.

Authors:  Qiang Du; Qin Sun; Xiaodong Gu; Jinchao Wang; Weitao Li; Luo Guo; Huawei Li
Journal:  BMC Med Genomics       Date:  2022-06-17       Impact factor: 3.622

3.  Utility of Whole Genome Sequencing for Population Screening of Deafness-Related Genetic Variants and Cytomegalovirus Infection in Newborns.

Authors:  Jiale Xiang; Hongfu Zhang; Xiangzhong Sun; Junqing Zhang; Zhenpeng Xu; Jun Sun; Zhiyu Peng
Journal:  Front Genet       Date:  2022-04-29       Impact factor: 4.772

4.  Clinical Heterogeneity Associated with MYO7A Variants Relies on Affected Domains.

Authors:  Sun Young Joo; Gina Na; Jung Ah Kim; Jee Eun Yoo; Da Hye Kim; Se Jin Kim; Seung Hyun Jang; Seyoung Yu; Hye-Youn Kim; Jae Young Choi; Heon Yung Gee; Jinsei Jung
Journal:  Biomedicines       Date:  2022-03-29

5.  Comprehensive genetic testing improves the clinical diagnosis and medical management of pediatric patients with isolated hearing loss.

Authors:  Jiale Xiang; Yuan Jin; Nana Song; Sen Chen; Jiankun Shen; Wen Xie; Xiangzhong Sun; Zhiyu Peng; Yu Sun
Journal:  BMC Med Genomics       Date:  2022-06-27       Impact factor: 3.622

6.  GenOtoScope: Towards automating ACMG classification of variants associated with congenital hearing loss.

Authors:  Damianos P Melidis; Christian Landgraf; Gunnar Schmidt; Anja Schöner-Heinisch; Sandra von Hardenberg; Anke Lesinski-Schiedat; Wolfgang Nejdl; Bernd Auber
Journal:  PLoS Comput Biol       Date:  2022-09-21       Impact factor: 4.779

  6 in total

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