Evidence map›Paper›PMID 35786716›Full record

ArticleBioinformatics (Oxford, England)2022

ChromDMM: a Dirichlet-multinomial mixture model for clustering heterogeneous epigenetic data.

Maria Osmala, Gökçen Eraslan, Harri Lähdesmäki

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Maria OsmalaDepartment of Computer Science, Aalto University, Espoo 02150, Finland.ORCID 0000-0003-0128-4896
Gökçen EraslanKlarman Cell Observatory, Broad Institute of Harvard and MIT, Cambridge, MA 02142, USA.ORCID 0000-0001-9579-2909
Harri LähdesmäkiDepartment of Computer Science, Aalto University, Espoo 02150, Finland.

Funding

Academy of Finland 314445Finnish Cultural Foundation
6 · The paper itself

Abstract

motivationResearch on epigenetic modifications and other chromatin features at genomic regulatory elements elucidates essential biological mechanisms including the regulation of gene expression. Despite the growing number of epigenetic datasets, new tools are still needed to discover novel distinctive patterns of heterogeneous epigenetic signals at regulatory elements.

resultsWe introduce ChromDMM, a product Dirichlet-multinomial mixture model for clustering genomic regions that are characterized by multiple chromatin features. ChromDMM extends the mixture model framework by profile shifting and flipping that can probabilistically account for inaccuracies in the position and strand-orientation of the genomic regions. Owing to hyper-parameter optimization, ChromDMM can also regularize the smoothness of the epigenetic profiles across the consecutive genomic regions. With simulated data, we demonstrate that ChromDMM clusters, shifts and strand-orients the profiles more accurately than previous methods. With ENCODE data, we show that the clustering of enhancer regions in the human genome reveals distinct patterns in several chromatin features. We further validate the enhancer clusters by their enrichment for transcriptional regulatory factor binding sites. AVAILABILITY AND IMPLEMENTATION: ChromDMM is implemented as an R package and is available at https://github.com/MariaOsmala/ChromDMM. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Indexed as

EpigenomicsGenome, HumanChromatinCluster AnalysisEpigenesis, GeneticHumansChromatin

Identifiers

PMID35786716
PMCPMC9364382

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.