LDICDL: LncRNA-Disease Association Identification Based on Collaborative Deep Learning

被引:48
|
作者
Lan, Wei [1 ,2 ]
Lai, Dehuan [1 ]
Chen, Qingfeng [1 ,3 ]
Wu, Ximin [1 ]
Chen, Baoshan [3 ]
Liu, Jin [4 ]
Wang, Jianxin [4 ]
Chen, Yi-Ping Phoebe [5 ]
机构
[1] Guangxi Univ, Sch Comp Elect & Informat, Nanning 530004, Guangxi, Peoples R China
[2] Guangxi Univ, Guangxi Key Lab Multimedia Commun & Network Techn, Nanning 530004, Guangxi, Peoples R China
[3] Guangxi Univ, State Key Lab Conservat & Utilizat Subtrop Agrobi, Nanning 530004, Guangxi, Peoples R China
[4] Cent South Univ, Sch Comp Sci & Engn, Hunan Prov Key Lab Bioinformat, Changsha 410083, Hunan, Peoples R China
[5] La Trobe Univ, Dept Comp Sci & Informat Technol, Melbourne, Vic 3086, Australia
基金
中国国家自然科学基金;
关键词
Diseases; Matrix decomposition; RNA; Prediction algorithms; Noise reduction; Biological system modeling; Computational modeling; lncRNA-disease associations; matrix factorization; stacked denoising autoencoder; LONG NONCODING RNAS; OSTEOSARCOMA; NETWORKS; MECHANISMS; EVOLUTION; PATTERNS; MICRORNA; PROMOTES; DATABASE; GENE;
D O I
10.1109/TCBB.2020.3034910
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
It has been proved that long noncoding RNA (lncRNA) plays critical roles in many human diseases. Therefore, inferring associations between lncRNAs and diseases can contribute to disease diagnosis, prognosis and treatment. To overcome the limitation of traditional experimental methods such as expensive and time-consuming, several computational methods have been proposed to predict lncRNA-disease associations by fusing different biological data. However, the prediction performance of lncRNA-disease associations identification needs to be improved. In this study, we propose a computational model (named LDICDL) to identify lncRNA-disease associations based on collaborative deep learning. It uses an automatic encoder to denoise multiple lncRNA feature information and multiple disease feature information, respectively. Then, the matrix decomposition algorithm is employed to predict the potential lncRNA-disease associations. In addition, to overcome the limitation of matrix decomposition, the hybrid model is developed to predict associations between new lncRNA (or disease) and diseases (or lncRNA). The ten-fold cross validation and de novo test are applied to evaluate the performance of method. The experimental results show LDICDL outperforms than other state-of-the-art methods in prediction performance.
引用
收藏
页码:1715 / 1723
页数:9
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