Collaborative deep learning improves disease-related circRNA prediction based on multi-source functional information

被引:27
作者
Wang, Yongtian [1 ]
Liu, Xinmeng [1 ]
Shen, Yewei [1 ]
Song, Xuerui [2 ]
Wang, Tao [1 ]
Shang, Xuequn [1 ]
Peng, Jiajie [1 ]
机构
[1] Northwestern Polytech Univ, Sch Comp Sci, Xian 710072, Peoples R China
[2] Xian Childrens Hosp, Childrens Hlth prevent Dept, Xian, Peoples R China
基金
中国国家自然科学基金;
关键词
circRNA; disease; multi-view functional annotation; collaborative deep learning; BLADDER-CANCER; HEPATOCELLULAR-CARCINOMA; COMPLEX DISEASES; NONCODING RNAS; ASSOCIATIONS; EXPRESSION; NETWORK; CIRCHIPK3; LNCRNA; HSA-CIRC-0000711;
D O I
10.1093/bib/bbad069
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Emerging studies have shown that circular RNAs (circRNAs) are involved in a variety of biological processes and play a key role in disease diagnosing, treating and inferring. Although many methods, including traditional machine learning and deep learning, have been developed to predict associations between circRNAs and diseases, the biological function of circRNAs has not been fully exploited. Some methods have explored disease-related circRNAs based on different views, but how to efficiently use the multi-view data about circRNA is still not well studied. Therefore, we propose a computational model to predict potential circRNA-disease associations based on collaborative learning with circRNA multi-view functional annotations. First, we extract circRNA multi-view functional annotations and build circRNA association networks, respectively, to enable effective network fusion. Then, a collaborative deep learning framework for multi-view information is designed to get circRNA multi-source information features, which can make full use of the internal relationship among circRNA multi-view information. We build a network consisting of circRNAs and diseases by their functional similarity and extract the consistency description information of circRNAs and diseases. Last, we predict potential associations between circRNAs and diseases based on graph auto encoder. Our computational model has better performance in predicting candidate disease-related circRNAs than the existing ones. Furthermore, it shows the high practicability of the method that we use several common diseases as case studies to find some unknown circRNAs related to them. The experiments show that CLCDA can efficiently predict disease-related circRNAs and are helpful for the diagnosis and treatment of human disease.
引用
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页数:14
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