ReviewCellular and molecular life sciences : CMLS2025
Deep learning in chromatin organization: from super-resolution microscopy to clinical applications.
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.
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.
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.
Who cites it
2 citing papers in PubMed.
- RAD21 regulation of the enhancer-promoter chromatin loop of RAD51 promotes PARPi resistance in ovarian cancer.Journal of translational medicine · 2026Article
- Illuminating the genome: emerging approaches in CRISPR-Cas live-cell imaging.Nucleic acids research · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
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
Identifiers
What OpenQuestion holds
Registered trials
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.