Evidence map›Paper›PMID 41840705›Full record

ArticleGenomics & informatics2026

scCAPReSE: detection of large-scale genomic rearrangements from single-cell Hi-C based on few-shot learning.

Kyukwang Kim, Chul-Hwan Lee, Inkyung Jung

Abstract read
In one paragraph

Article in Genomics & informatics, 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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1 · What the graph read from it

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2 · The registry

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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.

Kyukwang KimDepartment of Biological Sciences, Korea Advanced Institute of Science and Technology, Daejeon, Republic of Korea.ORCID http://orcid.org/0000-0001-5571-4949
Chul-Hwan LeeDepartment of Biomedical Sciences and Pharmacology, Seoul National University College of Medicine, Seoul, Republic of Korea. chulhwan@snu.ac.kr.ORCID http://orcid.org/0000-0003-0643-0100
Inkyung JungDepartment of Biological Sciences, Korea Advanced Institute of Science and Technology, Daejeon, Republic of Korea. ijung@kaist.ac.kr.ORCID http://orcid.org/0000-0002-5885-2754

Funding

National Research Foundation in Republic of Korea RS-2023-00223069National Research Foundation in Republic of Korea RS-2025-02214225NAVER-SNUH 37-2024-2170
6 · The paper itself

Abstract

Large-scale genomic rearrangements are prevalent in cancer genomes and can profoundly rewire three-dimensional (3D) genome architecture, leading to aberrant oncogene activation through enhancer hijacking. The rewired 3D organization generates unique chromatin contact signatures, which can be detected using deep learning-based approaches. However, extending such analyses to single-cell resolution, which is critical to delineate clonal heterogeneity in cancer, remains a major challenge, due to the limited number of training sets as single-cell Hi-C techniques are not standardized and only limited datasets are available across different methods. Here, we introduce scCAPReSE, a few-shot learning-based framework that adopts representations from a pre-trained image foundation model, CLIP, to enable robust classification of structural variation (SV) patterns in single-cell Hi-C data. By extracting and fine-tuning base weights from the foundation model, scCAPReSE enables effective training of deep learning classifiers using only a few hundred large-scale SV examples derived from a single cancer cell line while adapting classification tasks to heterogeneous single-cell Hi-C libraries. scCAPReSE achieved over 90% classification accuracy when evaluated on sci-Hi-C datasets. When further applied to scNanoHi-C data from the K562 chronic myeloid leukemia cell line, scCAPReSE correctly identified the Philadelphia chromosome translocation but also revealed substantial cell-to-cell variability in the contribution of SV-mediated chromatin interactions, highlighting previously inaccessible heterogeneity in cancer 3D genome organization. In summary, scCAPReSE provides a broadly applicable and data-efficient framework for detecting SV-driven 3D genome reorganization at single-cell resolution, enabling quantitative dissection of cancer-specific chromatin architecture and clonal heterogeneity. The developed method is freely available at https://github.com/kaistcbfg/CAPReSE.

Indexed as

3D genomeCancerFew-shot learningFoundation modelSingle-cell Hi-CStructural variation

Identifiers

PMID41840705
PMCPMC13104498

What Socratic holds

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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 Socratic graph.