| Literature DB >> 31241222 |
Alin Voskanian1, Panagiotis Katsonis2, Olivier Lichtarge2,3, Vikas Pejaver4,5, Predrag Radivojac6, Sean D Mooney4, Emidio Capriotti7, Yana Bromberg8,9,10, Yanran Wang8, Max Miller8, Pier Luigi Martelli11, Castrense Savojardo11, Giulia Babbi11, Rita Casadio11, Yue Cao12, Yuanfei Sun12, Yang Shen12, Aditi Garg13, Debnath Pal13, Yao Yu14, Chad D Huff14, Sean V Tavtigian15, Erin Young15, Susan L Neuhausen16, Elad Ziv17, Lipika R Pal18, Gaia Andreoletti19, Steven E Brenner19, Maricel G Kann1.
Abstract
The availability of disease-specific genomic data is critical for developing new computational methods that predict the pathogenicity of human variants and advance the field of precision medicine. However, the lack of gold standards to properly train and benchmark such methods is one of the greatest challenges in the field. In response to this challenge, the scientific community is invited to participate in the Critical Assessment for Genome Interpretation (CAGI), where unpublished disease variants are available for classification by in silico methods. As part of the CAGI-5 challenge, we evaluated the performance of 18 submissions and three additional methods in predicting the pathogenicity of single nucleotide variants (SNVs) in checkpoint kinase 2 (CHEK2) for cases of breast cancer in Hispanic females. As part of the assessment, the efficacy of the analysis method and the setup of the challenge were also considered. The results indicated that though the challenge could benefit from additional participant data, the combined generalized linear model analysis and odds of pathogenicity analysis provided a framework to evaluate the methods submitted for SNV pathogenicity identification and for comparison to other available methods. The outcome of this challenge and the approaches used can help guide further advancements in identifying SNV-disease relationships.Entities:
Keywords: CAGI; CHEK2; Hispanic women; SNV; breast cancer
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Year: 2019 PMID: 31241222 PMCID: PMC6744287 DOI: 10.1002/humu.23849
Source DB: PubMed Journal: Hum Mutat ISSN: 1059-7794 Impact factor: 4.700