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An enhanced variant effect predictor based on a deep generative model and the Born-Again Networks
The development of an accurate and reliable variant effect prediction tool is important for research in human genetic diseases. A large number of predictors have been developed towards this goal, yet many of these predictors suffer from the problem of data circularity. Here we present MTBAN (Mutatio...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8476491/ https://www.ncbi.nlm.nih.gov/pubmed/34580383 http://dx.doi.org/10.1038/s41598-021-98693-3 |
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author | Kim, Ha Young Jeon, Woosung Kim, Dongsup |
author_facet | Kim, Ha Young Jeon, Woosung Kim, Dongsup |
author_sort | Kim, Ha Young |
collection | PubMed |
description | The development of an accurate and reliable variant effect prediction tool is important for research in human genetic diseases. A large number of predictors have been developed towards this goal, yet many of these predictors suffer from the problem of data circularity. Here we present MTBAN (Mutation effect predictor using the Temporal convolutional network and the Born-Again Networks), a method for predicting the deleteriousness of variants. We apply a form of knowledge distillation technique known as the Born-Again Networks (BAN) to a previously developed deep autoregressive generative model, mutationTCN, to achieve an improved performance in variant effect prediction. As the model is fully unsupervised and trained only on the evolutionarily related sequences of a protein, it does not suffer from the problem of data circularity which is common across supervised predictors. When evaluated on a test dataset consisting of deleterious and benign human protein variants, MTBAN shows an outstanding predictive ability compared to other well-known variant effect predictors. We also offer a user-friendly web server to predict variant effects using MTBAN, freely accessible at http://mtban.kaist.ac.kr. To our knowledge, MTBAN is the first variant effect prediction tool based on a deep generative model that provides a user-friendly web server for the prediction of deleteriousness of variants. |
format | Online Article Text |
id | pubmed-8476491 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-84764912021-09-29 An enhanced variant effect predictor based on a deep generative model and the Born-Again Networks Kim, Ha Young Jeon, Woosung Kim, Dongsup Sci Rep Article The development of an accurate and reliable variant effect prediction tool is important for research in human genetic diseases. A large number of predictors have been developed towards this goal, yet many of these predictors suffer from the problem of data circularity. Here we present MTBAN (Mutation effect predictor using the Temporal convolutional network and the Born-Again Networks), a method for predicting the deleteriousness of variants. We apply a form of knowledge distillation technique known as the Born-Again Networks (BAN) to a previously developed deep autoregressive generative model, mutationTCN, to achieve an improved performance in variant effect prediction. As the model is fully unsupervised and trained only on the evolutionarily related sequences of a protein, it does not suffer from the problem of data circularity which is common across supervised predictors. When evaluated on a test dataset consisting of deleterious and benign human protein variants, MTBAN shows an outstanding predictive ability compared to other well-known variant effect predictors. We also offer a user-friendly web server to predict variant effects using MTBAN, freely accessible at http://mtban.kaist.ac.kr. To our knowledge, MTBAN is the first variant effect prediction tool based on a deep generative model that provides a user-friendly web server for the prediction of deleteriousness of variants. Nature Publishing Group UK 2021-09-27 /pmc/articles/PMC8476491/ /pubmed/34580383 http://dx.doi.org/10.1038/s41598-021-98693-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Kim, Ha Young Jeon, Woosung Kim, Dongsup An enhanced variant effect predictor based on a deep generative model and the Born-Again Networks |
title | An enhanced variant effect predictor based on a deep generative model and the Born-Again Networks |
title_full | An enhanced variant effect predictor based on a deep generative model and the Born-Again Networks |
title_fullStr | An enhanced variant effect predictor based on a deep generative model and the Born-Again Networks |
title_full_unstemmed | An enhanced variant effect predictor based on a deep generative model and the Born-Again Networks |
title_short | An enhanced variant effect predictor based on a deep generative model and the Born-Again Networks |
title_sort | enhanced variant effect predictor based on a deep generative model and the born-again networks |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8476491/ https://www.ncbi.nlm.nih.gov/pubmed/34580383 http://dx.doi.org/10.1038/s41598-021-98693-3 |
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