Evidence map›Paper›PMID 38565260›Full record

ArticleBioinformatics (Oxford, England)2024

EpiSegMix: a flexible distribution hidden Markov model with duration modeling for chromatin state discovery.

Johanna Elena Schmitz, Nihit Aggarwal, Lukas Laufer, Jörn Walter, Abdulrahman Salhab, Sven Rahmann

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Article
  3. NAR genomics and bioinformatics · 2025
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Johanna Elena SchmitzAlgorithmic Bioinformatics, Center for Bioinformatics Saar, Saarland Informatics Campus, 66123 Saarbrücken, Germany.ORCID 0009-0002-6377-2561
Nihit AggarwalDepartment of Genetics, Saarland University, 66123 Saarbrücken, Germany.
Lukas LauferDepartment of Genetics, Saarland University, 66123 Saarbrücken, Germany.
Jörn WalterDepartment of Genetics, Saarland University, 66123 Saarbrücken, Germany.ORCID 0000-0003-0563-7417
Abdulrahman SalhabDepartment of Genetics, Saarland University, 66123 Saarbrücken, Germany.
Sven RahmannAlgorithmic Bioinformatics, Center for Bioinformatics Saar, Saarland Informatics Campus, 66123 Saarbrücken, Germany.ORCID 0000-0002-8536-6065

Funding

ELIXIR-DE
6 · The paper itself

Abstract

motivationAutomated 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.

resultsWe 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 accurate probabilistic model, which has the potential to increase the biological interpretability of chromatin states. AVAILABILITY AND IMPLEMENTATION: Source code: https://gitlab.com/rahmannlab/episegmix.

Indexed as

ChromatinEpigenesis, GeneticHigh-Throughput Nucleotide SequencingHistonesSequence Analysis, DNASoftwareChromatinHistones

Identifiers

PMID38565260
PMCPMC11026141

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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.