ArticleOncotarget2017
Computational prediction of human disease-related microRNAs by path-based random walk.
Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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Who cites it
6 citing papers in PubMed.
- SCPLPA: An miRNA-disease association prediction model based on spatial consistency projection and label propagation algorithm.Journal of cellular and molecular medicine · 2024Article
- Prediction of miRNA-disease associations in microbes based on graph convolutional networks and autoencoders.Frontiers in microbiology · 2023Article
- MSFSP: A Novel miRNA-Disease Association Prediction Model by Federating Multiple-Similarities Fusion and Space Projection.Frontiers in genetics · 2020Article
- Dual Laplacian regularized matrix completion for microRNA-disease associations prediction.RNA biology · 2019Article
- Bipartite Heterogeneous Network Method Based on Co-neighbor for MiRNA-Disease Association Prediction.Frontiers in genetics · 2019Article
- A novel information diffusion method based on network consistency for identifying disease related microRNAs.RSC advances · 2018Article
Corrections and comments
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Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
MicroRNAs (miRNAs) are a class of small, endogenous RNAs that are 21-25 nucleotides in length. In animals and plants, miRNAs target specific genes for degradation or translation repression. Discovering disease-related miRNA is fundamental for understanding the pathogenesis of diseases. The association between miRNA and a disease is mainly determined via biological investigation, which is complicated by increased biological information due to big data from different databases. Researchers have utilized different computational methods to harmonize experimental approaches to discover miRNA that articulates restrictively in specific environmental situations. In this work, we present a prediction model that is based on the theory of path features and random walk to obtain a relevancy score of miRNA-related disease. In this model, highly ranked scores are potential miRNA-disease associations. Features were extracted from positive and negative samples of miRNA-disease association. Then, we compared our method with other presented models using the five-fold cross-validation method, which obtained an area under the receiver operating characteristic curve of 88.6%. This indicated that our method has a better performance compared to previous methods and will help future biological investigations.
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Registered trials
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