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A Bayesian framework for efficient and accurate variant prediction
There is a growing need to develop variant prediction tools capable of assessing a wide spectrum of evidence. We present a Bayesian framework that involves aggregating pathogenicity data across multiple in silico scores on a gene-by-gene basis and multiple evidence statistics in both quantitative an...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6136750/ https://www.ncbi.nlm.nih.gov/pubmed/30212499 http://dx.doi.org/10.1371/journal.pone.0203553 |
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author | Qian, Dajun Li, Shuwei Tian, Yuan Clifford, Jacob W. Sarver, Brice A. J. Pesaran, Tina Gau, Chia-Ling Elliott, Aaron M. Lu, Hsiao-Mei Black, Mary Helen |
author_facet | Qian, Dajun Li, Shuwei Tian, Yuan Clifford, Jacob W. Sarver, Brice A. J. Pesaran, Tina Gau, Chia-Ling Elliott, Aaron M. Lu, Hsiao-Mei Black, Mary Helen |
author_sort | Qian, Dajun |
collection | PubMed |
description | There is a growing need to develop variant prediction tools capable of assessing a wide spectrum of evidence. We present a Bayesian framework that involves aggregating pathogenicity data across multiple in silico scores on a gene-by-gene basis and multiple evidence statistics in both quantitative and qualitative forms, and performs 5-tiered variant classification based on the resulting probability credible interval. When evaluated in 1,161 missense variants, our gene-specific in silico model-based meta-predictor yielded an area under the curve (AUC) of 96.0% and outperformed all other in silico predictors. Multifactorial model analysis incorporating all available evidence yielded 99.7% AUC, with 22.8% predicted as variants of uncertain significance (VUS). Use of only 3 auto-computed evidence statistics yielded 98.6% AUC with 56.0% predicted as VUS, which represented sufficient accuracy to rapidly assign a significant portion of VUS to clinically meaningful classifications. Collectively, our findings support the use of this framework to conduct large-scale variant prioritization using in silico predictors followed by variant prediction and classification with a high degree of predictive accuracy. |
format | Online Article Text |
id | pubmed-6136750 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-61367502018-09-27 A Bayesian framework for efficient and accurate variant prediction Qian, Dajun Li, Shuwei Tian, Yuan Clifford, Jacob W. Sarver, Brice A. J. Pesaran, Tina Gau, Chia-Ling Elliott, Aaron M. Lu, Hsiao-Mei Black, Mary Helen PLoS One Research Article There is a growing need to develop variant prediction tools capable of assessing a wide spectrum of evidence. We present a Bayesian framework that involves aggregating pathogenicity data across multiple in silico scores on a gene-by-gene basis and multiple evidence statistics in both quantitative and qualitative forms, and performs 5-tiered variant classification based on the resulting probability credible interval. When evaluated in 1,161 missense variants, our gene-specific in silico model-based meta-predictor yielded an area under the curve (AUC) of 96.0% and outperformed all other in silico predictors. Multifactorial model analysis incorporating all available evidence yielded 99.7% AUC, with 22.8% predicted as variants of uncertain significance (VUS). Use of only 3 auto-computed evidence statistics yielded 98.6% AUC with 56.0% predicted as VUS, which represented sufficient accuracy to rapidly assign a significant portion of VUS to clinically meaningful classifications. Collectively, our findings support the use of this framework to conduct large-scale variant prioritization using in silico predictors followed by variant prediction and classification with a high degree of predictive accuracy. Public Library of Science 2018-09-13 /pmc/articles/PMC6136750/ /pubmed/30212499 http://dx.doi.org/10.1371/journal.pone.0203553 Text en © 2018 Qian et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Qian, Dajun Li, Shuwei Tian, Yuan Clifford, Jacob W. Sarver, Brice A. J. Pesaran, Tina Gau, Chia-Ling Elliott, Aaron M. Lu, Hsiao-Mei Black, Mary Helen A Bayesian framework for efficient and accurate variant prediction |
title | A Bayesian framework for efficient and accurate variant prediction |
title_full | A Bayesian framework for efficient and accurate variant prediction |
title_fullStr | A Bayesian framework for efficient and accurate variant prediction |
title_full_unstemmed | A Bayesian framework for efficient and accurate variant prediction |
title_short | A Bayesian framework for efficient and accurate variant prediction |
title_sort | bayesian framework for efficient and accurate variant prediction |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6136750/ https://www.ncbi.nlm.nih.gov/pubmed/30212499 http://dx.doi.org/10.1371/journal.pone.0203553 |
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