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Detecting differentially methylated loci for multiple treatments based on high-throughput methylation data
BACKGROUND: Because of its important effects, as an epigenetic factor, on gene expression and disease development, DNA methylation has drawn much attention from researchers. Detecting differentially methylated loci is an important but challenging step in studying the regulatory roles of DNA methylat...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4026834/ https://www.ncbi.nlm.nih.gov/pubmed/24884464 http://dx.doi.org/10.1186/1471-2105-15-142 |
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author | Chen, Zhongxue Huang, Hanwen Liu, Qingzhong |
author_facet | Chen, Zhongxue Huang, Hanwen Liu, Qingzhong |
author_sort | Chen, Zhongxue |
collection | PubMed |
description | BACKGROUND: Because of its important effects, as an epigenetic factor, on gene expression and disease development, DNA methylation has drawn much attention from researchers. Detecting differentially methylated loci is an important but challenging step in studying the regulatory roles of DNA methylation in a broad range of biological processes and diseases. Several statistical approaches have been proposed to detect significant methylated loci; however, most of them were designed specifically for case-control studies. RESULTS: Noticing that the age is associated with methylation level and the methylation data are not normally distributed, in this paper, we propose a nonparametric method to detect differentially methylated loci under multiple conditions with trend for Illumina Array Methylation data. The nonparametric method, Cuzick test is used to detect the differences among treatment groups with trend for each age group; then an overall p-value is calculated based on the method of combining those independent p-values each from one age group. CONCLUSIONS: We compare the new approach with other methods using simulated and real data. Our study shows that the proposed method outperforms other methods considered in this paper in term of power: it detected more biological meaningful differentially methylated loci than others. |
format | Online Article Text |
id | pubmed-4026834 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40268342014-05-30 Detecting differentially methylated loci for multiple treatments based on high-throughput methylation data Chen, Zhongxue Huang, Hanwen Liu, Qingzhong BMC Bioinformatics Methodology Article BACKGROUND: Because of its important effects, as an epigenetic factor, on gene expression and disease development, DNA methylation has drawn much attention from researchers. Detecting differentially methylated loci is an important but challenging step in studying the regulatory roles of DNA methylation in a broad range of biological processes and diseases. Several statistical approaches have been proposed to detect significant methylated loci; however, most of them were designed specifically for case-control studies. RESULTS: Noticing that the age is associated with methylation level and the methylation data are not normally distributed, in this paper, we propose a nonparametric method to detect differentially methylated loci under multiple conditions with trend for Illumina Array Methylation data. The nonparametric method, Cuzick test is used to detect the differences among treatment groups with trend for each age group; then an overall p-value is calculated based on the method of combining those independent p-values each from one age group. CONCLUSIONS: We compare the new approach with other methods using simulated and real data. Our study shows that the proposed method outperforms other methods considered in this paper in term of power: it detected more biological meaningful differentially methylated loci than others. BioMed Central 2014-05-15 /pmc/articles/PMC4026834/ /pubmed/24884464 http://dx.doi.org/10.1186/1471-2105-15-142 Text en Copyright © 2014 Chen et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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. |
spellingShingle | Methodology Article Chen, Zhongxue Huang, Hanwen Liu, Qingzhong Detecting differentially methylated loci for multiple treatments based on high-throughput methylation data |
title | Detecting differentially methylated loci for multiple treatments based on high-throughput methylation data |
title_full | Detecting differentially methylated loci for multiple treatments based on high-throughput methylation data |
title_fullStr | Detecting differentially methylated loci for multiple treatments based on high-throughput methylation data |
title_full_unstemmed | Detecting differentially methylated loci for multiple treatments based on high-throughput methylation data |
title_short | Detecting differentially methylated loci for multiple treatments based on high-throughput methylation data |
title_sort | detecting differentially methylated loci for multiple treatments based on high-throughput methylation data |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4026834/ https://www.ncbi.nlm.nih.gov/pubmed/24884464 http://dx.doi.org/10.1186/1471-2105-15-142 |
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