Prediction of miRNA-disease association based on multisource inductive matrix completion
MicroRNAs (miRNAs) are endogenous non-coding RNAs approximately 23 nucleotides in length, playing significant roles in various cellular processes. Numerous studies have shown that miRNAs are involved in the regulation of many human diseases. Accurate prediction of miRNA-disease associations is cruci...
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| Published in | Scientific reports Vol. 14; no. 1; pp. 27503 - 15 |
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| Main Authors | , |
| Format | Journal Article |
| Language | English |
| Published |
London
Nature Publishing Group UK
11.11.2024
Nature Publishing Group Nature Portfolio |
| Subjects | |
| Online Access | Get full text |
| ISSN | 2045-2322 2045-2322 |
| DOI | 10.1038/s41598-024-78212-w |
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| Summary: | MicroRNAs (miRNAs) are endogenous non-coding RNAs approximately 23 nucleotides in length, playing significant roles in various cellular processes. Numerous studies have shown that miRNAs are involved in the regulation of many human diseases. Accurate prediction of miRNA-disease associations is crucial for early diagnosis, treatment, and prognosis assessment of diseases. In this paper, we propose the Autoencoder Inductive Matrix Completion (AEIMC) model to identify potential miRNA-disease associations. The model captures interaction features from multiple similarity networks, including miRNA functional similarity, miRNA sequence similarity, disease semantic similarity, disease ontology similarity, and Gaussian interaction kernel similarity between miRNAs and diseases. Autoencoders are used to extract more complex and abstract data representations, which are then input into the inductive matrix completion model for association prediction. The effectiveness of the model is validated through cross-validation, stratified threshold evaluation, and case studies, while ablation experiments further confirm the necessity of introducing sequence and ontology similarities for the first time. |
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| Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
| ISSN: | 2045-2322 2045-2322 |
| DOI: | 10.1038/s41598-024-78212-w |