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Getting personal with epigenetics: towards individual-specific epigenomic imputation with machine learning
Epigenetic modifications are dynamic mechanisms involved in the regulation of gene expression. Unlike the DNA sequence, epigenetic patterns vary not only between individuals, but also between different cell types within an individual. Environmental factors, somatic mutations and ageing contribute to...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10406842/ https://www.ncbi.nlm.nih.gov/pubmed/37550323 http://dx.doi.org/10.1038/s41467-023-40211-2 |
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author | Hawkins-Hooker, Alex Visonà, Giovanni Narendra, Tanmayee Rojas-Carulla, Mateo Schölkopf, Bernhard Schweikert, Gabriele |
author_facet | Hawkins-Hooker, Alex Visonà, Giovanni Narendra, Tanmayee Rojas-Carulla, Mateo Schölkopf, Bernhard Schweikert, Gabriele |
author_sort | Hawkins-Hooker, Alex |
collection | PubMed |
description | Epigenetic modifications are dynamic mechanisms involved in the regulation of gene expression. Unlike the DNA sequence, epigenetic patterns vary not only between individuals, but also between different cell types within an individual. Environmental factors, somatic mutations and ageing contribute to epigenetic changes that may constitute early hallmarks or causal factors of disease. Epigenetic modifications are reversible and thus promising therapeutic targets for precision medicine. However, mapping efforts to determine an individual’s cell-type-specific epigenome are constrained by experimental costs and tissue accessibility. To address these challenges, we developed eDICE, an attention-based deep learning model that is trained to impute missing epigenomic tracks by conditioning on observed tracks. Using a recently published set of epigenomes from four individual donors, we show that transfer learning across individuals allows eDICE to successfully predict individual-specific epigenetic variation even in tissues that are unmapped in a given donor. These results highlight the potential of machine learning-based imputation methods to advance personalized epigenomics. |
format | Online Article Text |
id | pubmed-10406842 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-104068422023-08-09 Getting personal with epigenetics: towards individual-specific epigenomic imputation with machine learning Hawkins-Hooker, Alex Visonà, Giovanni Narendra, Tanmayee Rojas-Carulla, Mateo Schölkopf, Bernhard Schweikert, Gabriele Nat Commun Article Epigenetic modifications are dynamic mechanisms involved in the regulation of gene expression. Unlike the DNA sequence, epigenetic patterns vary not only between individuals, but also between different cell types within an individual. Environmental factors, somatic mutations and ageing contribute to epigenetic changes that may constitute early hallmarks or causal factors of disease. Epigenetic modifications are reversible and thus promising therapeutic targets for precision medicine. However, mapping efforts to determine an individual’s cell-type-specific epigenome are constrained by experimental costs and tissue accessibility. To address these challenges, we developed eDICE, an attention-based deep learning model that is trained to impute missing epigenomic tracks by conditioning on observed tracks. Using a recently published set of epigenomes from four individual donors, we show that transfer learning across individuals allows eDICE to successfully predict individual-specific epigenetic variation even in tissues that are unmapped in a given donor. These results highlight the potential of machine learning-based imputation methods to advance personalized epigenomics. Nature Publishing Group UK 2023-08-07 /pmc/articles/PMC10406842/ /pubmed/37550323 http://dx.doi.org/10.1038/s41467-023-40211-2 Text en © The Author(s) 2023 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Hawkins-Hooker, Alex Visonà, Giovanni Narendra, Tanmayee Rojas-Carulla, Mateo Schölkopf, Bernhard Schweikert, Gabriele Getting personal with epigenetics: towards individual-specific epigenomic imputation with machine learning |
title | Getting personal with epigenetics: towards individual-specific epigenomic imputation with machine learning |
title_full | Getting personal with epigenetics: towards individual-specific epigenomic imputation with machine learning |
title_fullStr | Getting personal with epigenetics: towards individual-specific epigenomic imputation with machine learning |
title_full_unstemmed | Getting personal with epigenetics: towards individual-specific epigenomic imputation with machine learning |
title_short | Getting personal with epigenetics: towards individual-specific epigenomic imputation with machine learning |
title_sort | getting personal with epigenetics: towards individual-specific epigenomic imputation with machine learning |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10406842/ https://www.ncbi.nlm.nih.gov/pubmed/37550323 http://dx.doi.org/10.1038/s41467-023-40211-2 |
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