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Potential circRNA-disease association prediction using DeepWalk and network consistency projection

一致性(知识库) 相似性(几何) 计算机科学 数据挖掘 投影(关系代数) 人工智能 疾病 机器学习 交叉验证 计算生物学 生物信息学 生物 算法 医学 病理 图像(数学)
作者
Guanghui Li,Jiawei Luo,Diancheng Wang,Cheng Liang,Qiu Xiao,Pingjian Ding,Hailin Chen
出处
期刊:Journal of Biomedical Informatics [Elsevier BV]
卷期号:112: 103624-103624 被引量:46
标识
DOI:10.1016/j.jbi.2020.103624
摘要

• We present a measurement to calculate the similarities for circRNAs and diseases. • A similarity-based model is proposed for excavating circRNA-disease associations. • The method does not need any additional biological features in the prediction process. • The method achieves impressive performance and can effectively predict novel disease circRNAs. A growing body of experimental studies have reported that circular RNAs (circRNAs) are of interest in pathogenicity mechanism research and are becoming new diagnostic biomarkers. As experimental techniques for identifying disease-circRNA interactions are costly and laborious, some computational predictors have been advanced on the basis of the integration of biological features about circRNAs and diseases. However, the existing circRNA-disease relationships are not well exploited. To solve this issue, a novel method named DeepWalk and network consistency projection for circRNA-disease association prediction (DWNCPCDA) is proposed. Specifically, our method first reveals features of nodes learned by the deep learning method DeepWalk based on known circRNA-disease associations to calculate circRNA-circRNA similarity and disease-disease similarity, and then these two similarity networks are further employed to feed to the network consistency projection method to predict unobserved circRNA-disease interactions. As a result, DWNCPCDA shows high-accuracy performances for disease-circRNA interaction prediction: an AUC of 0.9647 with leave-one-out cross validation and an average AUC of 0.9599 with five-fold cross validation. We further perform case studies to prioritize latent circRNAs related to complex human diseases. Overall, this proposed method is able to provide a promising solution for disease-circRNA interaction prediction, and is capable of enhancing existing similarity-based prediction methods.
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