Journal
FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY
Volume 9, Issue -, Pages -Publisher
FRONTIERS MEDIA SA
DOI: 10.3389/fcell.2021.617569
Keywords
miRNA; disease; miRNA– disease association; similarity network fusion; inductive matrix completion
Categories
Funding
- National Natural Science Foundation of China [U19A2064, 61873001, 61872220, 61861146002, 11701318]
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MicroRNAs, as non-coding RNAs, are closely related to complex biological processes and human diseases. The study introduced a novel model, SNFIMCMDA, combining similarity network fusion and inductive matrix completion. Global leave-one-out cross-validation and five-fold cross-validation were utilized to validate the model efficacy, with case studies on three human diseases supporting its effectiveness.
MicroRNAs (miRNAs) that belong to non-coding RNAs are verified to be closely associated with several complicated biological processes and human diseases. In this study, we proposed a novel model that was Similarity Network Fusion and Inductive Matrix Completion for miRNA-Disease Association Prediction (SNFIMCMDA). We applied inductive matrix completion (IMC) method to acquire possible associations between miRNAs and diseases, which also could obtain corresponding correlation scores. IMC was performed based on the verified connections of miRNA-disease, miRNA similarity, and disease similarity. In addition, miRNA similarity and disease similarity were calculated by similarity network fusion, which could masterly integrate multiple data types to obtain target data. We integrated miRNA functional similarity and Gaussian interaction profile kernel similarity by similarity network fusion to obtain miRNA similarity. Similarly, disease similarity was integrated in this way. To indicate the utility and effectiveness of SNFIMCMDA, we both applied global leave-one-out cross-validation and five-fold cross-validation to validate our model. Furthermore, case studies on three significant human diseases were also implemented to prove the effectiveness of SNFIMCMDA. The results demonstrated that SNFIMCMDA was effective for prediction of possible associations of miRNA-disease.
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