ArticleCells2022
SGAEMDA: Predicting miRNA-Disease Associations Based on Stacked Graph Autoencoder.
Article in Cells, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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Who cites it
4 citing papers in PubMed.
- Prediction of miRNA-disease associations based on PCA and cascade forest.BMC bioinformatics · 2024Article
- A Semi-Supervised Stacked Autoencoder Using the Pseudo Label for Classification Tasks.Entropy (Basel, Switzerland) · 2023Article
- MSGNN-DTA: Multi-Scale Topological Feature Fusion Based on Graph Neural Networks for Drug-Target Binding Affinity Prediction.International journal of molecular sciences · 2023Article
- A review of multi-omics data integration through deep learning approaches for disease diagnosis, prognosis, and treatment.Frontiers in genetics · 2023Review
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Authors and funding
7 authors.
Funding
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Abstract
MicroRNA (miRNA)-disease association (MDA) prediction is critical for disease prevention, diagnosis, and treatment. Traditional MDA wet experiments, on the other hand, are inefficient and costly.Therefore, we proposed a multi-layer collaborative unsupervised training base model called SGAEMDA (Stacked Graph Autoencoder-Based Prediction of Potential miRNA-Disease Associations). First, from the original miRNA and disease data, we defined two types of initial features: similarity features and association features. Second, stacked graph autoencoder is then used to learn unsupervised low-dimensional representations of meaningful higher-order similarity features, and we concatenate the association features with the learned low-dimensional representations to obtain the final miRNA-disease pair features. Finally, we used a multilayer perceptron (MLP) to predict scores for unknown miRNA-disease associations. SGAEMDA achieved a mean area under the ROC curve of 0.9585 and 0.9516 in 5-fold and 10-fold cross-validation, which is significantly higher than the other baseline methods. Furthermore, case studies have shown that SGAEMDA can accurately predict candidate miRNAs for brain, breast, colon, and kidney neoplasms.
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Registered trials
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