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On the prediction of non-CG DNA methylation using machine learning
DNA methylation can be detected and measured using sequencing instruments after sodium bisulfite conversion, but experiments can be expensive for large eukaryotic genomes. Sequencing nonuniformity and mapping biases can leave parts of the genome with low or no coverage, thus hampering the ability of...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10189801/ https://www.ncbi.nlm.nih.gov/pubmed/37206627 http://dx.doi.org/10.1093/nargab/lqad045 |
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author | Sereshki, Saleh Lee, Nathan Omirou, Michalis Fasoula, Dionysia Lonardi, Stefano |
author_facet | Sereshki, Saleh Lee, Nathan Omirou, Michalis Fasoula, Dionysia Lonardi, Stefano |
author_sort | Sereshki, Saleh |
collection | PubMed |
description | DNA methylation can be detected and measured using sequencing instruments after sodium bisulfite conversion, but experiments can be expensive for large eukaryotic genomes. Sequencing nonuniformity and mapping biases can leave parts of the genome with low or no coverage, thus hampering the ability of obtaining DNA methylation levels for all cytosines. To address these limitations, several computational methods have been proposed that can predict DNA methylation from the DNA sequence around the cytosine or from the methylation level of nearby cytosines. However, most of these methods are entirely focused on CG methylation in humans and other mammals. In this work, we study, for the first time, the problem of predicting cytosine methylation for CG, CHG and CHH contexts on six plant species, either from the DNA primary sequence around the cytosine or from the methylation levels of neighboring cytosines. In this framework, we also study the cross-species prediction problem and the cross-context prediction problem (within the same species). Finally, we show that providing gene and repeat annotations allows existing classifiers to significantly improve their prediction accuracy. We introduce a new classifier called AMPS (annotation-based methylation prediction from sequence) that takes advantage of genomic annotations to achieve higher accuracy. |
format | Online Article Text |
id | pubmed-10189801 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-101898012023-05-18 On the prediction of non-CG DNA methylation using machine learning Sereshki, Saleh Lee, Nathan Omirou, Michalis Fasoula, Dionysia Lonardi, Stefano NAR Genom Bioinform Standard Article DNA methylation can be detected and measured using sequencing instruments after sodium bisulfite conversion, but experiments can be expensive for large eukaryotic genomes. Sequencing nonuniformity and mapping biases can leave parts of the genome with low or no coverage, thus hampering the ability of obtaining DNA methylation levels for all cytosines. To address these limitations, several computational methods have been proposed that can predict DNA methylation from the DNA sequence around the cytosine or from the methylation level of nearby cytosines. However, most of these methods are entirely focused on CG methylation in humans and other mammals. In this work, we study, for the first time, the problem of predicting cytosine methylation for CG, CHG and CHH contexts on six plant species, either from the DNA primary sequence around the cytosine or from the methylation levels of neighboring cytosines. In this framework, we also study the cross-species prediction problem and the cross-context prediction problem (within the same species). Finally, we show that providing gene and repeat annotations allows existing classifiers to significantly improve their prediction accuracy. We introduce a new classifier called AMPS (annotation-based methylation prediction from sequence) that takes advantage of genomic annotations to achieve higher accuracy. Oxford University Press 2023-05-17 /pmc/articles/PMC10189801/ /pubmed/37206627 http://dx.doi.org/10.1093/nargab/lqad045 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of NAR Genomics and Bioinformatics. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Standard Article Sereshki, Saleh Lee, Nathan Omirou, Michalis Fasoula, Dionysia Lonardi, Stefano On the prediction of non-CG DNA methylation using machine learning |
title | On the prediction of non-CG DNA methylation using machine learning |
title_full | On the prediction of non-CG DNA methylation using machine learning |
title_fullStr | On the prediction of non-CG DNA methylation using machine learning |
title_full_unstemmed | On the prediction of non-CG DNA methylation using machine learning |
title_short | On the prediction of non-CG DNA methylation using machine learning |
title_sort | on the prediction of non-cg dna methylation using machine learning |
topic | Standard Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10189801/ https://www.ncbi.nlm.nih.gov/pubmed/37206627 http://dx.doi.org/10.1093/nargab/lqad045 |
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