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MomicPred: A Cell Cycle Prediction Framework Based on Dual-Branch Multi-Modal Feature Fusion for Single-Cell

Zhenqi Shi, Linxing Cong, Hao Wu

    IEEE Journal of Biomedical and Health Informatics
    |August 6, 2025
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    Summary

    Predicting cell cycle dynamics is crucial for stem cell differentiation. MomicPred integrates gene expression and 3D genome data for precise cell cycle prediction, revealing insights into chromatin structure and biological processes.

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    Area of Science:

    • Cell Biology
    • Genomics
    • Bioinformatics

    Background:

    • The cell cycle is critical for cell fate and stem cell differentiation, impacting tissue homeostasis.
    • Accurate cell cycle regulation is essential for maintaining cellular diversity.
    • Single-cell multi-omics technologies offer potential for improved cell cycle prediction by integrating gene expression and chromatin data.

    Purpose of the Study:

    • To develop an advanced computational framework for predicting cell cycle dynamics.
    • To effectively integrate transcriptome and 3D genome data for enhanced cell cycle prediction.
    • To uncover cross-layer associations between gene expression and chromatin structure in cell cycle regulation.

    Main Methods:

    • Proposed MomicPred, a dual-branch multi-modal fusion framework.
    • Integrated transcriptome-derived gene expression data with 3D genome structural insights.
    • Extracted three core feature sets to capture synergistic interactions between omics modalities.

    Main Results:

    • Achieved high-precision cell cycle prediction by leveraging complementary multi-omics data.
    • Demonstrated the efficiency and robustness of MomicPred through benchmarking.
    • Identified key biological processes and chromatin structural changes across distinct cell cycle stages.

    Conclusions:

    • MomicPred offers a novel approach for predicting cell cycle dynamics using integrated multi-omics data.
    • The framework provides new perspectives on the interplay between gene expression and chromatin structure.
    • Findings contribute to a deeper understanding of cell cycle regulation in stem cell differentiation and tissue homeostasis.