Journal article
Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification
MT Parsons, E Tudini, H Li, E Hahnen, B Wappenschmidt, L Feliubadaló, CM Aalfs, S Agata, K Aittomäki, E Alducci, MC Alonso-Cerezo, N Arnold, B Auber, R Austin, J Azzollini, J Balmaña, E Barbieri, CR Bartram, A Blanco, B Blümcke Show all
Human Mutation | WILEY | Published : 2019
DOI: 10.1002/humu.23818
Abstract
The multifactorial likelihood analysis method has demonstrated utility for quantitative assessment of variant pathogenicity for multiple cancer syndrome genes. Independent data types currently incorporated in the model for assessing BRCA1 and BRCA2 variants include clinically calibrated prior probability of pathogenicity based on variant location and bioinformatic prediction of variant effect, co-segregation, family cancer history profile, co-occurrence with a pathogenic variant in the same gene, breast tumor pathology, and case-control information. Research and clinical data for multifactorial likelihood analysis were collated for 1,395 BRCA1/2 predominantly intronic and missense variants, ..
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Grants
Awarded by National Breast Cancer Foundation