Abstract

BackgroundAn increasing number of studies have shown that lncRNAs are crucial for the control of hormones and the regulation of various physiological processes in the human body, and deletion mutations in RNA are related to many human diseases. LncRNA- disease association prediction is very useful for understanding pathogenesis, diagnosis, and prevention of diseases, and is helpful for labelling relevant biological information.ResultsIn this manuscript, we propose a computational model named bidirectional generative adversarial network (BiGAN), which consists of an encoder, a generator, and a discriminator to predict new lncRNA-disease associations. We construct features between lncRNA and disease pairs by utilizing the disease semantic similarity, lncRNA sequence similarity, and Gaussian interaction profile kernel similarities of lncRNAs and diseases. The BiGAN maps the latent features of similarity features to predict unverified association between lncRNAs and diseases. The computational results have proved that the BiGAN performs significantly better than other state-of-the-art approaches in cross-validation. We employed the proposed model to predict candidate lncRNAs for renal cancer and colon cancer. The results are promising. Case studies show that almost 70% of lncRNAs in the top 10 prediction lists are verified by recent biological research.ConclusionThe experimental results indicated that our proposed model had an accurate predictive ability for the association of lncRNA-disease pairs.

Highlights

  • An increasing number of studies have shown that long non-coding RNAs (lncRNAs) are crucial for the control of hormones and the regulation of various physiological processes in the human body, and deletion mutations in RNA are related to many human diseases

  • We integrated lncRNA sequence similarity, disease semantic similarity, and Gaussian interaction profile kernel similarity to mine the high-level representation of the potential space between lncRNAs and diseases

  • The bidirectional generative adversarial network (BiGAN) can effectively predict the associations between lncRNAs based on the latent relationship of the integrated similarity vectors

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Summary

Introduction

An increasing number of studies have shown that lncRNAs are crucial for the control of hormones and the regulation of various physiological processes in the human body, and deletion mutations in RNA are related to many human diseases. LncRNA- disease association prediction is very useful for understanding pathogenesis, diagnosis, and prevention of diseases, and is helpful for labelling relevant biological information. An increasing number of studies have revealed that protein-coding genes account for only a tiny fraction of human genome (approximately 1.5%), while the other human genes are not involved in the protein-coding sequence [2,3,4,5]. In recent years, an increasing amount of experimental evidence has demonstrated that in most biological processes non-coding. It can help us to understand the biological processes and the molecular mechanisms of human diseases from the perspective of ncRNAs

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