Abstract

BackgroundMicroRNAs (miRNAs) have been confirmed to have close relationship with various human complex diseases. The identification of disease-related miRNAs provides great insights into the underlying pathogenesis of diseases. However, it is still a big challenge to identify which miRNAs are related to diseases. As experimental methods are in general expensive and time‐consuming, it is important to develop efficient computational models to discover potential miRNA-disease associations.MethodsThis study presents a novel prediction method called HFHLMDA, which is based on high-dimensionality features and hypergraph learning, to reveal the association between diseases and miRNAs. Firstly, the miRNA functional similarity and the disease semantic similarity are integrated to form an informative high-dimensionality feature vector. Then, a hypergraph is constructed by the K-Nearest-Neighbor (KNN) method, in which each miRNA-disease pair and its k most relevant neighbors are linked as one hyperedge to represent the complex relationships among miRNA-disease pairs. Finally, the hypergraph learning model is designed to learn the projection matrix which is used to calculate uncertain miRNA-disease association score.ResultCompared with four state-of-the-art computational models, HFHLMDA achieved best results of 92.09% and 91.87% in leave-one-out cross validation and fivefold cross validation, respectively. Moreover, in case studies on Esophageal neoplasms, Hepatocellular Carcinoma, Breast Neoplasms, 90%, 98%, and 96% of the top 50 predictions have been manually confirmed by previous experimental studies.ConclusionMiRNAs have complex connections with many human diseases. In this study, we proposed a novel computational model to predict the underlying miRNA-disease associations. All results show that the proposed method is effective for miRNA–disease association predication.

Highlights

  • IntroductionMicroRNAs (miRNAs) have been confirmed to have close relationship with various human complex diseases

  • MicroRNAs have been confirmed to have close relationship with various human complex diseases

  • We proposed a novel computational model to predict the underlying miRNA-disease associations

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Summary

Introduction

MicroRNAs (miRNAs) have been confirmed to have close relationship with various human complex diseases. As experimental methods are in general expensive and time‐consuming, it is important to develop efficient computational models to discover potential miRNA-disease associations. Identifying diseaserelated miRNAs is important to treat, diagnose, and prevent human complex diseases [8, 9]. Researchers use biological experimental methods such as quantitative reverse transcription, microarray analysis, or deep sequencing of small RNAs to explore miRNAs that are differentially expressed in a disease state. Based on vast amount of biological data about miRNAs, researchers have developed computational methods for predicting miRNA-disease associations [11,12,13,14,15,16,17,18,19,20,21], which can select most promising miRNAs for further analysis and decrease the number of the experiments

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