Evidence map›Paper›PMID 40879746›Full record

ReviewCellular and molecular life sciences : CMLS2025

Deep learning in chromatin organization: from super-resolution microscopy to clinical applications.

Mikhail Rotkevich, Carlotta Viana, Maria Victoria Neguembor, Maria Pia Cosma

Abstract readReview
In one paragraph

Review in Cellular and molecular life sciences : CMLS, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

2 citing papers in PubMed.

  1. Article
  2. Review
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

4 authors.

Mikhail Rotkevich *Centre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, Barcelona, 08003, Spain.ORCID http://orcid.org/0000-0002-1650-7688
Carlotta Viana *Centre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, Barcelona, 08003, Spain.ORCID http://orcid.org/0000-0002-7160-5491
Maria Victoria NeguemborCentre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, Barcelona, 08003, Spain. vnebmc@ibmb.csic.es.ORCID http://orcid.org/0000-0002-1583-1304
Maria Pia CosmaCentre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, Barcelona, 08003, Spain. pia.cosma@crg.eu.ORCID http://orcid.org/0000-0003-4207-5097

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The 3D organization of the genome plays a critical role in regulating gene expression, maintaining cellular identity, and mediating responses to environmental cues. Advances in super-resolution microscopy and genomic technologies have enabled unprecedented insights into chromatin architecture at nanoscale resolution. However, the complexity and volume of data generated by these techniques necessitate innovative computational strategies for effective analysis and interpretation. In this review, we explore the transformative role of deep learning in the analysis of 3D genome organization, highlighting how deep learning models are being leveraged to enhance image reconstruction, segmentation, and dynamic tracking in chromatin research. We provide an overview of deep learning-enhanced methodologies that significantly improve spatial and temporal resolution of images, with a special focus on single-molecule localization microscopy. Furthermore, we discuss deep learning's contribution to segmentation accuracy, and its application in single-particle tracking for dissecting chromatin dynamics at the single-cell level. These advances are complemented by frameworks that enable multimodal integration and interpretability, pushing the boundaries of chromatin biology into clinical diagnostics and personalized medicine. Finally, we discuss emerging clinical applications where deep learning models, based on chromatin imaging, aid in disease stratification, drug response prediction, and early cancer detection. We also address the challenges of data sparsity, model interpretability and propose future directions to decode genome function with higher precision and impact.

Indexed as

ChromatinDeep LearningMicroscopyAnimalsHumansImage Processing, Computer-AssistedChromatinArtificial intelligence (AI)Chromatin structureConvolutional neural networks (CNNs)Fluorescence imagingImage restorationImage segmentationLive-cell analysisMolecular diagnosticsNuclear organizationSingle molecule localization microscopy (SMLM)Single-particle tracking (SPT)STORMSuper-resolution microscopy (SRM)Transformer architectures

Identifiers

PMID40879746
PMCPMC12397471

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.