ArticleMolecular therapy. Nucleic acids2019
Self-Weighted Multi-Kernel Multi-Label Learning for Potential miRNA-Disease Association Prediction.
Article in Molecular therapy. Nucleic acids, 2019. 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.
- Machine learning in the development of targeting microRNAs in human disease.Frontiers in genetics · 2022Review
- TSMDA: Target and symptom-based computational model for miRNA-disease-association prediction.Molecular therapy. Nucleic acids · 2021Article
- Predicting miRNA-Disease Associations Based on Heterogeneous Graph Attention Networks.Frontiers in genetics · 2021Article
- Multiview Consensus Graph Learning for lncRNA-Disease Association Prediction.Frontiers in genetics · 2020Article
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Authors and funding
7 authors.
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Abstract
Researchers have realized that microRNAs (miRNAs) play significant roles in the pathogenesis of various diseases. Although many computational models have been proposed to predict the associations between miRNAs and diseases, prediction performance could still be improved. In this paper, we propose a novel self-weighted, multi-kernel, multi-label learning (SwMKML) method to predict disease-related miRNAs. SwMKML adaptively learns two optimal kernel matrices for both miRNAs and diseases from multiple kernels constructed from known miRNA-disease associations. Moreover, the miRNA-disease associations predicted from both spaces are updated simultaneously based on a multi-label framework. Compared with four state-of-the-art computational models, SwMKML achieved best results of 95.5%, 93.1%, and 84.1% in global leave-one-out cross-validation, 5-fold cross-validation, and overall prediction accuracy, respectively. A case study conducted on head and neck neoplasms further identified two potential prognostic biomarkers, hsa-mir-125b-1 and hsa-mir-125b-2, for the disease. SwMKML is freely available at Github, and we anticipate that it may become an effective tool for potential miRNA-disease association prediction.
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