Evidence map›Paper›PMID 41875404›Full record

ArticlePLoS computational biology2026

HiCMamba: Enhancing Hi-C resolution and identifying 3D genome structures with state space modeling.

Minghao Yang, Zhi-An Huang, Zhihang Zheng, Yuqiao Liu, Shichen Zhang, Pengfei Zhang, Hui Xiong, Shaojun Tang

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Article in PLoS computational biology, 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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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Minghao YangArtificial Intelligence Thrust, Hong Kong University of Science and Technology (Guangzhou), Guangzhou, China.
Zhi-An HuangDepartment of Computer Science, City University of Hong Kong (Dongguan), Dongguan, China.
Zhihang ZhengBioscience and Biomedical Engineering Thrust, Hong Kong University of Science and Technology (Guangzhou), Guangzhou, China.
Yuqiao LiuBioscience and Biomedical Engineering Thrust, Hong Kong University of Science and Technology (Guangzhou), Guangzhou, China.
Shichen ZhangBioscience and Biomedical Engineering Thrust, Hong Kong University of Science and Technology (Guangzhou), Guangzhou, China.
Pengfei ZhangArtificial Intelligence Thrust, Hong Kong University of Science and Technology (Guangzhou), Guangzhou, China.
Hui XiongArtificial Intelligence Thrust, Hong Kong University of Science and Technology (Guangzhou), Guangzhou, China.
Shaojun TangDepartment of Biostatistics, Virginia Commonwealth University, Richmond, Virginia, United States of America.ORCID https://orcid.org/0000-0002-5141-0515

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hi-C technology measures genome-wide interaction frequencies, providing a powerful tool for studying the 3D genomic structure within the nucleus. However, high sequencing costs and technical challenges often result in Hi-C data with limited coverage, leading to imprecise estimates of chromatin interaction frequencies. To address this issue, we present a novel deep learning-based method HiCMamba to enhance the resolution of Hi-C contact maps using a state space model. We adopt the UNet-based auto-encoder architecture to stack the proposed holistic scan block, enabling the perception of both global and local receptive fields at multiple scales. Experimental results demonstrate that HiCMamba outperforms state-of-the-art methods while significantly reducing computational resources. Furthermore, the 3D genome structures, including topologically associating domains (TADs) and loops, identified in the contact maps recovered by HiCMamba are validated through associated epigenomic features. Our work demonstrates the potential of a state space model as foundational frameworks in the field of Hi-C resolution enhancement. The data and source code used in this work are available at GitHub: https://github.com/myang998/HiCMamba.

Indexed as

Deep LearningGenomeGenomicsAnimalsChromatinComputational BiologyHumansChromatin

Identifiers

PMID41875404
PMCPMC13012732

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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.