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MethylNet: an automated and modular deep learning approach for DNA methylation analysis
BACKGROUND: DNA methylation (DNAm) is an epigenetic regulator of gene expression programs that can be altered by environmental exposures, aging, and in pathogenesis. Traditional analyses that associate DNAm alterations with phenotypes suffer from multiple hypothesis testing and multi-collinearity du...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7076991/ https://www.ncbi.nlm.nih.gov/pubmed/32183722 http://dx.doi.org/10.1186/s12859-020-3443-8 |
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author | Levy, Joshua J. Titus, Alexander J. Petersen, Curtis L. Chen, Youdinghuan Salas, Lucas A. Christensen, Brock C. |
author_facet | Levy, Joshua J. Titus, Alexander J. Petersen, Curtis L. Chen, Youdinghuan Salas, Lucas A. Christensen, Brock C. |
author_sort | Levy, Joshua J. |
collection | PubMed |
description | BACKGROUND: DNA methylation (DNAm) is an epigenetic regulator of gene expression programs that can be altered by environmental exposures, aging, and in pathogenesis. Traditional analyses that associate DNAm alterations with phenotypes suffer from multiple hypothesis testing and multi-collinearity due to the high-dimensional, continuous, interacting and non-linear nature of the data. Deep learning analyses have shown much promise to study disease heterogeneity. DNAm deep learning approaches have not yet been formalized into user-friendly frameworks for execution, training, and interpreting models. Here, we describe MethylNet, a DNAm deep learning method that can construct embeddings, make predictions, generate new data, and uncover unknown heterogeneity with minimal user supervision. RESULTS: The results of our experiments indicate that MethylNet can study cellular differences, grasp higher order information of cancer sub-types, estimate age and capture factors associated with smoking in concordance with known differences. CONCLUSION: The ability of MethylNet to capture nonlinear interactions presents an opportunity for further study of unknown disease, cellular heterogeneity and aging processes. |
format | Online Article Text |
id | pubmed-7076991 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-70769912020-03-18 MethylNet: an automated and modular deep learning approach for DNA methylation analysis Levy, Joshua J. Titus, Alexander J. Petersen, Curtis L. Chen, Youdinghuan Salas, Lucas A. Christensen, Brock C. BMC Bioinformatics Methodology Article BACKGROUND: DNA methylation (DNAm) is an epigenetic regulator of gene expression programs that can be altered by environmental exposures, aging, and in pathogenesis. Traditional analyses that associate DNAm alterations with phenotypes suffer from multiple hypothesis testing and multi-collinearity due to the high-dimensional, continuous, interacting and non-linear nature of the data. Deep learning analyses have shown much promise to study disease heterogeneity. DNAm deep learning approaches have not yet been formalized into user-friendly frameworks for execution, training, and interpreting models. Here, we describe MethylNet, a DNAm deep learning method that can construct embeddings, make predictions, generate new data, and uncover unknown heterogeneity with minimal user supervision. RESULTS: The results of our experiments indicate that MethylNet can study cellular differences, grasp higher order information of cancer sub-types, estimate age and capture factors associated with smoking in concordance with known differences. CONCLUSION: The ability of MethylNet to capture nonlinear interactions presents an opportunity for further study of unknown disease, cellular heterogeneity and aging processes. BioMed Central 2020-03-17 /pmc/articles/PMC7076991/ /pubmed/32183722 http://dx.doi.org/10.1186/s12859-020-3443-8 Text en © The Author(s). 2020 Open AccessThis 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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Methodology Article Levy, Joshua J. Titus, Alexander J. Petersen, Curtis L. Chen, Youdinghuan Salas, Lucas A. Christensen, Brock C. MethylNet: an automated and modular deep learning approach for DNA methylation analysis |
title | MethylNet: an automated and modular deep learning approach for DNA methylation analysis |
title_full | MethylNet: an automated and modular deep learning approach for DNA methylation analysis |
title_fullStr | MethylNet: an automated and modular deep learning approach for DNA methylation analysis |
title_full_unstemmed | MethylNet: an automated and modular deep learning approach for DNA methylation analysis |
title_short | MethylNet: an automated and modular deep learning approach for DNA methylation analysis |
title_sort | methylnet: an automated and modular deep learning approach for dna methylation analysis |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7076991/ https://www.ncbi.nlm.nih.gov/pubmed/32183722 http://dx.doi.org/10.1186/s12859-020-3443-8 |
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