<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zheng Y</submitter><funding>RRD VA</funding><funding>NIMH NIH HHS</funding><funding>Biomedical Laboratory Research and Development, VA Office of Research and Development</funding><funding>National Institute of Mental Health</funding><pagination>2241-2258</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9665129</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>17(13)</volume><pubmed_abstract>Differentially methylated regions (DMRs) are genomic regions with specific methylation patterns across multiple loci that are associated with a phenotype. We examined the genome-wide false positive (GFP) rates of five widely used DMR methods: comb-p, Bumphunter, DMRcate, mCSEA and coMethDMR using both Illumina HumanMethylation450 (450 K) and MethylationEPIC (EPIC) data and simulated continuous and dichotomous null phenotypes (i.e., generated independently of methylation data). coMethDMR provided well-controlled GFP rates (~5%) except when analysing skewed continuous phenotypes. DMRcate generally had well-controlled GFP rates when applied to 450 K data except for the skewed continuous phenotype and EPIC data only for the normally distributed continuous phenotype. GFP rates for mCSEA were at</pubmed_abstract><journal>Epigenetics</journal><pubmed_title>An evaluation of the genome-wide false positive rates of common methods for identifying differentially methylated regions using illumina methylation arrays.</pubmed_title><pmcid>PMC9665129</pmcid><funding_grant_id>R21 MH102834</funding_grant_id><funding_grant_id>R21MH102834</funding_grant_id><funding_grant_id>1R01MH108826</funding_grant_id><funding_grant_id>R01 MH108826</funding_grant_id><funding_grant_id>I50 RX003001</funding_grant_id><funding_grant_id>I01BX003477</funding_grant_id><pubmed_authors>Miller MW</pubmed_authors><pubmed_authors>Zheng Y</pubmed_authors><pubmed_authors>Katrinli S</pubmed_authors><pubmed_authors>Logue MW</pubmed_authors><pubmed_authors>Liu C</pubmed_authors><pubmed_authors>Lunetta KL</pubmed_authors><pubmed_authors>Smith AK</pubmed_authors></additional><is_claimable>false</is_claimable><name>An evaluation of the genome-wide false positive rates of common methods for identifying differentially methylated regions using illumina methylation arrays.</name><description>Differentially methylated regions (DMRs) are genomic regions with specific methylation patterns across multiple loci that are associated with a phenotype. We examined the genome-wide false positive (GFP) rates of five widely used DMR methods: comb-p, Bumphunter, DMRcate, mCSEA and coMethDMR using both Illumina HumanMethylation450 (450 K) and MethylationEPIC (EPIC) data and simulated continuous and dichotomous null phenotypes (i.e., generated independently of methylation data). coMethDMR provided well-controlled GFP rates (~5%) except when analysing skewed continuous phenotypes. DMRcate generally had well-controlled GFP rates when applied to 450 K data except for the skewed continuous phenotype and EPIC data only for the normally distributed continuous phenotype. GFP rates for mCSEA were at</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2026-05-28T01:31:40.956Z</modification><creation>2025-02-19T01:18:01.749Z</creation></dates><accession>S-EPMC9665129</accession><cross_references><pubmed>36047742</pubmed><doi>10.1080/15592294.2022.2115600</doi></cross_references></HashMap>