<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>40(4)</volume><submitter>Schmitz JE</submitter><funding>ELIXIR-DE</funding><pubmed_abstract>&lt;h4>Motivation&lt;/h4>Automated chromatin segmentation based on ChIP-seq (chromatin immunoprecipitation followed by sequencing) data reveals insights into the epigenetic regulation of chromatin accessibility. Existing segmentation methods are constrained by simplifying modeling assumptions, which may have a negative impact on the segmentation quality.&lt;h4>Results&lt;/h4>We introduce EpiSegMix, a novel segmentation method based on a hidden Markov model with flexible read count distribution types and state duration modeling, allowing for a more flexible modeling of both histone signals and segment lengths. In a comparison with existing tools, ChromHMM, Segway, and EpiCSeg, we show that EpiSegMix is more predictive of cell biology, such as gene expression. Its flexible framework enables it to fit an</pubmed_abstract><journal>Bioinformatics (Oxford, England)</journal><pagination>btae178</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11026141</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>EpiSegMix: a flexible distribution hidden Markov model with duration modeling for chromatin state discovery.</pubmed_title><pmcid>PMC11026141</pmcid><pubmed_authors>Rahmann S</pubmed_authors><pubmed_authors>Laufer L</pubmed_authors><pubmed_authors>Aggarwal N</pubmed_authors><pubmed_authors>Walter J</pubmed_authors><pubmed_authors>Salhab A</pubmed_authors><pubmed_authors>Schmitz JE</pubmed_authors></additional><is_claimable>false</is_claimable><name>EpiSegMix: a flexible distribution hidden Markov model with duration modeling for chromatin state discovery.</name><description>&lt;h4>Motivation&lt;/h4>Automated chromatin segmentation based on ChIP-seq (chromatin immunoprecipitation followed by sequencing) data reveals insights into the epigenetic regulation of chromatin accessibility. Existing segmentation methods are constrained by simplifying modeling assumptions, which may have a negative impact on the segmentation quality.&lt;h4>Results&lt;/h4>We introduce EpiSegMix, a novel segmentation method based on a hidden Markov model with flexible read count distribution types and state duration modeling, allowing for a more flexible modeling of both histone signals and segment lengths. In a comparison with existing tools, ChromHMM, Segway, and EpiCSeg, we show that EpiSegMix is more predictive of cell biology, such as gene expression. Its flexible framework enables it to fit an</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2026-05-29T11:26:10.228Z</modification><creation>2026-04-08T04:28:15.523Z</creation></dates><accession>S-EPMC11026141</accession><cross_references><pubmed>38565260</pubmed><doi>10.1093/bioinformatics/btae178</doi></cross_references></HashMap>