计算机科学
图形
人工神经网络
订单(交换)
人工智能
理论计算机科学
财务
经济
作者
Chen Jiang,Lei Wang,Chang-Qing Yu,Zhuhong You,Xinfei Wang,Mengmeng Wei,Mengmeng Lu
标识
DOI:10.1109/tbdata.2025.3604175
摘要
Circular RNAs (circRNAs) are non-coding RNA molecules that play a crucial role in regulating genes and contributing to disease progression. CircRNAs can function as sponges for microRNAs (miRNAs), thereby regulating gene expression and influencing disease outcomes. Identifying associations between circRNAs and miRNAs through computational methods enhances the understanding of complex disease mechanisms and offers a reliable tool for pre-selecting candidates for experimental validation. Existing models, however, are limited in their ability to capture either global or local node information, the prediction of circRNA and miRNA interactions is still challenging. In order to effectively deal with this problem, we propose a novel framework for predicting circRNA-miRNA interactions (CMIs), known as MuGNet-CMI, which leverages multi-head hybrid graph neural network and global high-order and local low-order information. The model employs the MetaPath2Vec algorithm to generate high-quality node embeddings within the circRNA-miRNA heterogeneous matrix. The multi-head dynamic attention mechanism, combined with GraphSAGE, is incorporated to efficiently capture both global high-order and local low-order node information. Additionally, we integrate neural aggregators into the multi-head dynamic attention mechanism to aggregate feature information from the captured nodes. Validation using three real datasets demonstrates that MuGNet-CMI delivers good performance in predicting CMIs, offering valuable insights to guide experimental research in gene regulation.
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