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    Area of Science:

    • Bioinformatics
    • Computational Biology
    • Genomics

    Background:

    • Long non-coding RNAs (lncRNAs) play critical roles in disease pathogenesis.
    • Accurate prediction of lncRNA-disease associations aids biological research and therapeutic target identification.
    • Existing prediction methods often neglect multi-scale graph information.

    Purpose of the Study:

    • To develop an advanced graph neural network framework for predicting lncRNA-disease associations.
    • To integrate global structural, local subgraph, and multi-scale graph information for enhanced prediction accuracy.
    • To introduce GLALDA, a novel prediction framework utilizing multi-scale graph-level attention.

    Main Methods:

    • Designed a graph neural network (GNN) prediction framework named GLALDA.
    • Employed a dual-level attention mechanism to integrate global and local graph information.
    • Incorporated edge features and cross-attention for multi-scale feature fusion.

    Main Results:

    • GLALDA achieved high performance with AUC of 0.949 and AUPR of 0.947 on public datasets.
    • Outperformed six state-of-the-art methods in lncRNA-disease association prediction.
    • Case studies on three cancers validated GLALDA's ability to identify potential disease-related lncRNAs.

    Conclusions:

    • GLALDA effectively predicts lncRNA-disease associations by integrating multi-scale graph information.
    • The framework offers a promising tool for advancing biological research and clinical applications.
    • GLALDA enhances efficiency and precision in identifying novel therapeutic targets.