This site is under development. For the current active site, go to bcbhub.csic.es.

Orcid Publication

Detalle de: mCSEA: detecting subtle differentially methylated regions

Title mCSEA: detecting subtle differentially methylated regions
Abstract

Motivation The identification of differentially methylated regions (DMRs) among phenotypes is one of the main goals of epigenetic analysis. Although there are several methods developed to detect DMRs, most of them are focused on detecting relatively large differences in methylation levels and fail to detect moderate, but consistent, methylation changes that might be associated to complex disorders. Results We present mCSEA, an R package that implements a Gene Set Enrichment Analysis method to identify DMRs from Illumina450K and EPIC array data. It is especially useful for detecting subtle, but consistent, methylation differences in complex phenotypes. mCSEA also implements functions to integrate gene expression data and to detect genes with significant correlations among methylation and gene expression patterns. Using simulated datasets we show that mCSEA outperforms other tools in detecting DMRs. In addition, we applied mCSEA to a previously published dataset of sibling pairs discordant for intrauterine hyperglycemia exposure. We found several differentially methylated promoters in genes related to metabolic disorders like obesity and diabetes, demonstrating the potential of mCSEA to identify DMRs not detected by other methods. Availability and implementation mCSEA is freely available from the Bioconductor repository. Supplementary information Supplementary data are available at Bioinformatics online.

Apa Reference Martorell-Marugán, J., González-Rumayor, V. & Carmona-Sáez, P. (2019). mCSEA: detecting subtle differentially methylated regions. Bioinformatics, 35(18), 3257-3262. 10.1093/bioinformatics/btz096
Doi 10.1093/bioinformatics/btz096
Publication Date 12 Feb 2019
Publication Type Article
Researcher Pedro Carmona-Saez
Ontology Transcriptomics, Bioinformatics Software and Tools, Analysis packages (R, Python, etc.), Functional annotation, Expression Profiling, Epigenomics, DNA methylation, Regulatory biology
Research Groups
Tools

Suggest changes

Publications are synced automatically from ORCID, so they can't be edited here directly. Spotted something wrong? Let us know below and we'll take care of it.

← Return to Home