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DGAMDA: Predicting miRNA-disease association based on dynamic graph attention network.

ChangXin Jia1, FuYu Wang2, Baoxiang Xing3

  • 1Department of Anesthesiology, the Affiliated Hospital of Qingdao University, Qingdao, People's Republic of China.

International Journal for Numerical Methods in Biomedical Engineering
|March 13, 2024
PubMed
Summary

This study introduces DGAMDA, a novel computational model for predicting microRNA (miRNA)-disease associations. DGAMDA enhances early disease screening by improving feature mining and prediction accuracy using dynamic graph attention.

Keywords:
dynamic graph attentionheterogeneous graph attention networkmicroRNA‐disease association

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Area of Science:

  • Computational biology
  • Bioinformatics
  • Genomics

Background:

  • Traditional experimental validation for microRNA (miRNA)-disease associations is time-consuming and costly.
  • Computational methods leveraging artificial intelligence offer efficient alternatives for predicting miRNA-disease associations.
  • Existing methods often struggle with feature heterogeneity and insufficient feature mining from static networks.

Purpose of the Study:

  • To propose a dynamic graph attention-based association prediction model (DGAMDA) for enhanced miRNA-disease association prediction.
  • To address limitations of static graph attention mechanisms in feature mining and heterogeneity.
  • To achieve high-precision feature mining and association scoring using a single miRNA-disease association network.

Main Methods:

  • Developed DGAMDA, a model integrating feature mapping and dynamic graph attention mechanisms.
  • Employed feature mining on a single miRNA-disease association network.
  • Conducted rigorous five-fold cross-validation experiments to evaluate model performance.

Main Results:

  • DGAMDA demonstrated high-precision feature mining and association scoring.
  • Achieved mean Accuracy of 0.8986, Precision of 0.8869, Recall of 0.9115, and F1-score of 0.8984.
  • Outperformed other advanced models in prediction accuracy and effectiveness.

Conclusions:

  • DGAMDA effectively overcomes feature heterogeneity and inadequate mining issues present in static models.
  • The model shows significant promise for accurate miRNA-disease association prediction and early disease screening.
  • DGAMDA can be utilized for predicting miRNAs associated with novel or unknown diseases.