Making the accurate prediction of miRNA-disease associations essential for medical interventions. Current computational models often fail to capture the complexity of miRNA-disease associations. This study proposes HHMDA, a method based on heterogeneous hypergraph convolution and heterogeneous graph multi-scale convolution, to predict the association between miRNA and disease. Firstly, HHMDA constructs a heterogeneous graph of miRNA-disease relationships. Then, a graph convolution is run on the heterogeneous graph to capture the multi-scale feature representations of miRNA and disease. MiRNA-disease association are reconstructed based on these features. Meanwhile, HHMDA constructs a heterogeneous hypergraph with miRNAs and diseases as nodes, and the hyperedges consist of miRNAs and diseases linked to the same genes. HHMDA performs hypergraph graph convolution operation on the heterogeneous hypergraph to extract the high-order features of miRNA and disease. Finally, these features are leveraged to calculate the Laplacian regularization loss and combined with the miRNA-disease association matrix reconstruction loss to optimize the model. The experimental results show that HHMDA has advantages over the existing state-of-the-art methods under different experimental settings.
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http://dx.doi.org/10.1007/s13755-024-00319-1 | DOI Listing |
Bioinformatics
December 2024
School of Data Science and Society, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, United States.
Motivation: Forecasting the synergistic effects of drug combinations facilitates drug discovery and development, especially regarding cancer therapeutics. While numerous computational methods have emerged, most of them fall short in fully modeling the relationships among clinical entities including drugs, cell lines, and diseases, which hampers their ability to generalize to drug combinations involving unseen drugs. These relationships are complex and multidimensional, requiring sophisticated modeling to capture nuanced interplay that can significantly influence therapeutic efficacy.
View Article and Find Full Text PDFHealth Inf Sci Syst
December 2025
Department of Computing Sciences, The College at Brockport, State University of New York, 350 New Campus Drive, Brockport, NY 14422 USA.
Making the accurate prediction of miRNA-disease associations essential for medical interventions. Current computational models often fail to capture the complexity of miRNA-disease associations. This study proposes HHMDA, a method based on heterogeneous hypergraph convolution and heterogeneous graph multi-scale convolution, to predict the association between miRNA and disease.
View Article and Find Full Text PDFJ Comput Biol
December 2024
Computer Engineering Department, University of Qom, Qom, Iran.
Developing a new drug is a long and expensive process that typically takes 10-15 years and costs billions of dollars. This has led to an increasing interest in drug repositioning, which involves finding new therapeutic uses for existing drugs. Computational methods become an increasingly important tool for identifying associations between drugs and new diseases.
View Article and Find Full Text PDFIEEE/ACM Trans Comput Biol Bioinform
October 2024
MicroRNAs (miRNAs) play a significant role in cell differentiation, biological development as well as the occurrence and growth of diseases. Although many computational methods contribute to predicting the association between miRNAs and diseases, they do not fully explore the attribute information contained in associated edges between miRNAs and diseases. In this study, we propose a new method, Hierarchical Hypergraph learning in Association-Weighted heterogeneous network for MiRNA-Disease association identification (HHAWMD).
View Article and Find Full Text PDFBioinformatics
September 2024
School of Information Science and Engineering, Yanshan University, Qinhuangdao 066004, China.
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