ArticleFrontiers in genetics2018
LLCMDA: A Novel Method for Predicting miRNA Gene and Disease Relationship Based on Locality-Constrained Linear Coding.
Article in Frontiers in genetics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed.
- An efficient model for predicting human diseases through miRNA based on multiple-types of contrastive learning.Frontiers in microbiology · 2023Article
- Article
- Article
- Heterogeneous Graph Convolutional Networks and Matrix Completion for miRNA-Disease Association Prediction.Frontiers in bioengineering and biotechnology · 2020Article
- LLCLPLDA: a novel model for predicting lncRNA-disease associations.Molecular genetics and genomics : MGG · 2019Article
- Benchmark of computational methods for predicting microRNA-disease associations.Genome biology · 2019Article
- Adaptive multi-view multi-label learning for identifying disease-associated candidate miRNAs.PLoS computational biology · 2019Article
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4 authors.
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Abstract
MiRNAs are small non-coding regulatory RNAs which are associated with multiple diseases. Increasing evidence has shown that miRNAs play important roles in various biological and physiological processes. Therefore, the identification of potential miRNA-disease associations could provide new clues to understanding the mechanism of pathogenesis. Although many traditional methods have been successfully applied to discover part of the associations, they are in general time-consuming and expensive. Consequently, computational-based methods are urgently needed to predict the potential miRNA-disease associations in a more efficient and resources-saving way. In this paper, we propose a novel method to predict miRNA-disease associations based on Locality-constrained Linear Coding (LLC). Specifically, we first reconstruct similarity networks for both miRNAs and diseases using LLC and then apply label propagation on the similarity networks to get relevant scores. To comprehensively verify the performance of the proposed method, we compare our method with several state-of-the-art methods under different evaluation metrics. Moreover, two types of case studies conducted on two common diseases further demonstrate the validity and utility of our method. Extensive experimental results indicate that our method can effectively predict potential associations between miRNAs and diseases.
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