Evidence map›Paper›PMID 41507775›Full record

ArticleBMC bioinformatics2026

From 2D to 4D: a containerized workflow and browser to explore dynamic chromatin architecture.

David H Rogers, Cullen Roth, Cameron Tauxe, Jeannie T Lee, Christina R Steadman, Karissa Y Sanbonmatsu, Anna Lappala, Shawn R Starkenburg

Abstract read
In one paragraph

Article in BMC bioinformatics, 2026. 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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0citing papers in PubMed
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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

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3 · Its place in the literature

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

David H RogersInformation Sciences Group, Los Alamos National Laboratory, Los Alamos, NM, US. dhr@lanl.gov.
Cullen RothGenomics & Bioanalytics Group, Los Alamos National Laboratory, Los Alamos, NM, US.
Cameron TauxeInformation Sciences Group, Los Alamos National Laboratory, Los Alamos, NM, US.
Jeannie T LeeDepartment of Molecular Biology, Massachusetts General Hospital, Boston, MA, US.
Christina R SteadmanGenomics & Bioanalytics Group, Los Alamos National Laboratory, Los Alamos, NM, US.
Karissa Y SanbonmatsuTheoretical Biology & Biophysics Group, Los Alamos National Laboratory, Los Alamos, NM, US.
Anna LappalaDepartment of Molecular Biology, Massachusetts General Hospital, Boston, MA, US.
Shawn R StarkenburgGenomics & Bioanalytics Group, Los Alamos National Laboratory, Los Alamos, NM, US. shawns@lanl.gov.

Funding

Spreading of Xist RNA and Polycomb complexes along the inactive X-chromosome.R01HD097665 · NICHD · MASSACHUSETTS GENERAL HOSPITAL · PI LEE, JEANNIE T · 2019 to 2023
$3.5M
Los Alamos National Laboratory Directed Research Grant 20210082DRNICHD NIH HHS R01 HD097665United States, National Institute of Health R01-HD097665U.S. Department of Energy, Office of Science, through the Biological and Environmental Research (BER) and the Advanced Scientific Computing Research (ASCR) programs 89233218CNA000001
6 · The paper itself

Abstract

backgroundCharacterizing the physical organization of the genome is essential for understanding long-range gene regulation, chromatin compartmentalization, and epigenetic accessibility. Hi-C experiments generate two-dimensional (2D) genome-wide contact maps of chromatin interactions by capturing the spatial proximity between genomic loci, which reveal interaction frequencies but lack the spatial resolution needed to interpret the three-dimensional (3D) genome structure(s). Emerging evidence suggests that epigenetic regulation is closely linked to 3D genome architecture, and that structural changes over time (4D) drive key biological processes in development, disease, and environmental response. Thus, integrating 3D structure with functional data is critical for a more complete understanding of genome regulation. Previous work, most notably the 4DHiC chromosome modeling framework, has shown that physical multi-dimensional modeling approaches rooted in polymer physics and molecular dynamics can resolve these structures at biologically meaningful resolutions by integrating temporal Hi-C data with physical constraints to uncover dynamic chromosome reorganization. Thus, molecular dynamics simulations, constrained by Hi-C contact matrices, can resolve fine-scale structural changes and reveal functionally significant transitions in chromatin conformation.

resultsHerein, we present the 4D Genome Browser Workflow (4DGBWorkflow) and the 4D Genome Browser (4DGB). The algorithm is based on the 4DHiC method, and the containerized tool is an end-to-end workflow that can transform, filter, and view 4D epigenomics and chromatin datasets, allowing non-specialists to apply three-dimensional modeling principles to diverse datasets and experimental conditions. The software executes on a laptop running macOS, Linux or Windows. From input Hi-C files (.hic), the 4DGBWorkflow produces 3D reconstructions of chromosomes, integrates the reconstruction with track data (e.g., epigenetic marks, transcriptome profiles), and provides comparative visualization of the results in a single workflow.

conclusionsThe 4DGBWorkflow and 4D Genome Browser are open-source tools for comparative analysis and visualization of 4D chromosome datasets, including chromatin architecture and epigenomic signals. Automatic integration of Hi-C data with molecular dynamics democratizes the construction of time resolved 3D genome structures, simplifying complex simulations and data integration schemes.

Indexed as

ChromatinSoftwareGenomeGenomicsHumansMolecular Dynamics SimulationWorkflowChromatin3D visualization4D genome browserChromatin architectureEpigenomicsGenome modelingHi-C

Identifiers

PMID41507775
PMCPMC12870729

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LicenceCC BY-NC-ND
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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.