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Genome-wide enhancer prediction from epigenetic signatures using genetic algorithm-optimized support vector machines
The chemical modification of histones at specific DNA regulatory elements is linked to the activation, inactivation and poising of genes. A number of tools exist to predict enhancers from chromatin modification maps, but their practical application is limited because they either (i) consider a small...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3378905/ https://www.ncbi.nlm.nih.gov/pubmed/22328731 http://dx.doi.org/10.1093/nar/gks149 |
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author | Fernández, Michael Miranda-Saavedra, Diego |
author_facet | Fernández, Michael Miranda-Saavedra, Diego |
author_sort | Fernández, Michael |
collection | PubMed |
description | The chemical modification of histones at specific DNA regulatory elements is linked to the activation, inactivation and poising of genes. A number of tools exist to predict enhancers from chromatin modification maps, but their practical application is limited because they either (i) consider a smaller number of marks than those necessary to define the various enhancer classes or (ii) work with an excessive number of marks, which is experimentally unviable. We have developed a method for chromatin state detection using support vector machines in combination with genetic algorithm optimization, called ChromaGenSVM. ChromaGenSVM selects optimum combinations of specific histone epigenetic marks to predict enhancers. In an independent test, ChromaGenSVM recovered 88% of the experimentally supported enhancers in the pilot ENCODE region of interferon gamma-treated HeLa cells. Furthermore, ChromaGenSVM successfully combined the profiles of only five distinct methylation and acetylation marks from ChIP-seq libraries done in human CD4(+) T cells to predict ∼21 000 experimentally supported enhancers within 1.0 kb regions and with a precision of ∼90%, thereby improving previous predictions on the same dataset by 21%. The combined results indicate that ChromaGenSVM comfortably outperforms previously published methods and that enhancers are best predicted by specific combinations of histone methylation and acetylation marks. |
format | Online Article Text |
id | pubmed-3378905 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-33789052012-06-20 Genome-wide enhancer prediction from epigenetic signatures using genetic algorithm-optimized support vector machines Fernández, Michael Miranda-Saavedra, Diego Nucleic Acids Res Methods Online The chemical modification of histones at specific DNA regulatory elements is linked to the activation, inactivation and poising of genes. A number of tools exist to predict enhancers from chromatin modification maps, but their practical application is limited because they either (i) consider a smaller number of marks than those necessary to define the various enhancer classes or (ii) work with an excessive number of marks, which is experimentally unviable. We have developed a method for chromatin state detection using support vector machines in combination with genetic algorithm optimization, called ChromaGenSVM. ChromaGenSVM selects optimum combinations of specific histone epigenetic marks to predict enhancers. In an independent test, ChromaGenSVM recovered 88% of the experimentally supported enhancers in the pilot ENCODE region of interferon gamma-treated HeLa cells. Furthermore, ChromaGenSVM successfully combined the profiles of only five distinct methylation and acetylation marks from ChIP-seq libraries done in human CD4(+) T cells to predict ∼21 000 experimentally supported enhancers within 1.0 kb regions and with a precision of ∼90%, thereby improving previous predictions on the same dataset by 21%. The combined results indicate that ChromaGenSVM comfortably outperforms previously published methods and that enhancers are best predicted by specific combinations of histone methylation and acetylation marks. Oxford University Press 2012-05 2012-02-10 /pmc/articles/PMC3378905/ /pubmed/22328731 http://dx.doi.org/10.1093/nar/gks149 Text en © The Author(s) 2012. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methods Online Fernández, Michael Miranda-Saavedra, Diego Genome-wide enhancer prediction from epigenetic signatures using genetic algorithm-optimized support vector machines |
title | Genome-wide enhancer prediction from epigenetic signatures using genetic algorithm-optimized support vector machines |
title_full | Genome-wide enhancer prediction from epigenetic signatures using genetic algorithm-optimized support vector machines |
title_fullStr | Genome-wide enhancer prediction from epigenetic signatures using genetic algorithm-optimized support vector machines |
title_full_unstemmed | Genome-wide enhancer prediction from epigenetic signatures using genetic algorithm-optimized support vector machines |
title_short | Genome-wide enhancer prediction from epigenetic signatures using genetic algorithm-optimized support vector machines |
title_sort | genome-wide enhancer prediction from epigenetic signatures using genetic algorithm-optimized support vector machines |
topic | Methods Online |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3378905/ https://www.ncbi.nlm.nih.gov/pubmed/22328731 http://dx.doi.org/10.1093/nar/gks149 |
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