ArticleBMC bioinformatics2014
Detecting differentially methylated loci for multiple treatments based on high-throughput methylation data.
Article in BMC bioinformatics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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Who cites it
4 citing papers in PubMed, 6 citations in OpenAlex.
- A novel family of beta mixture models for the differential analysis of DNA methylation data: An application to prostate cancer.PloS one · 2024Article
- Data-Driven-Based Approach to Identifying Differentially Methylated Regions Using Modified 1D Ising Model.BioMed research international · 2018Article
- Simultaneous statistical inference for epigenetic data.PloS one · 2015Article
- A new statistical approach to combining p-values using gamma distribution and its application to genome-wide association study.BMC bioinformatics · 2014Article
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Authors and funding
3 authors at 3 institutions in 1 country.
Funding
Abstract
backgroundBecause 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.
resultsNoticing 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.
conclusionsWe 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.
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