ArticleFrontiers in microbiology2023
Prediction of miRNA-disease associations in microbes based on graph convolutional networks and autoencoders.
Article in Frontiers in microbiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed.
- Leveraging explainable multi-scale features for fine-grained circRNA-miRNA interaction prediction.BMC biology · 2025Article
- Predicting noncoding RNA and disease associations using multigraph contrastive learning.Scientific reports · 2025Article
- Article
- HGSMDA: miRNA-Disease Association Prediction Based on HyperGCN and Sørensen-Dice Loss.Non-coding RNA · 2024Article
- Accurate identification of snoRNA targets using variational graph autoencoder to advance the redevelopment of traditional medicines.Frontiers in pharmacology · 2024Article
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Authors and funding
5 authors.
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Abstract
MicroRNAs (miRNAs) are short RNA molecular fragments that regulate gene expression by targeting and inhibiting the expression of specific RNAs. Due to the fact that microRNAs affect many diseases in microbial ecology, it is necessary to predict microRNAs' association with diseases at the microbial level. To this end, we propose a novel model, termed as GCNA-MDA, where dual-autoencoder and graph convolutional network (GCN) are integrated to predict miRNA-disease association. The proposed method leverages autoencoders to extract robust representations of miRNAs and diseases and meantime exploits GCN to capture the topological information of miRNA-disease networks. To alleviate the impact of insufficient information for the original data, the association similarity and feature similarity data are combined to calculate a more complete initial basic vector of nodes. The experimental results on the benchmark datasets demonstrate that compared with the existing representative methods, the proposed method has achieved the superior performance and its precision reaches up to 0.8982. These results demonstrate that the proposed method can serve as a tool for exploring miRNA-disease associations in microbial environments.
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