Predicting LncRNA-Disease Association Based on Generative Adversarial Network

被引:11
|
作者
Du, Biao [1 ,2 ]
Tang, Lin [2 ]
Liu, Lin [1 ,2 ]
Zhou, Wei [3 ]
机构
[1] Yunnan Normal Univ, Sch Informat, Kunming, Yunnan, Peoples R China
[2] Yunnan Normal Univ, Key Lab Educ Informatizat Nationalities, Minist Educ, Kunming, Yunnan, Peoples R China
[3] Yunnan Univ, Sch Software, Kunming, Yunnan, Peoples R China
基金
中国国家自然科学基金;
关键词
Generate adversarial network; LncRNA; disease; pairwise loss; generator; discriminator; LONG NONCODING RNAS;
D O I
10.2174/1566523221666210506131055
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background: Increasing research reveals that long non-coding RNAs (lncRNAs) play an important role in various biological processes of human diseases. Nonetheless, only a handful of lncRNA-disease associations have been experimentally verified. The study of lncRNA-disease association prediction based on the computational model has provided a preliminary basis for biological experiments to a great degree so as to cut down the huge cost of wet lab experiments. Objective: This study aims to learn the real distribution of lncRNA-disease association from a limited number of known lncRNA-disease association data. This paper proposes a new lncRNA-disease association prediction model called LDA-GAN based on a Generative Adversarial Network (GAN). Methods: Aiming at the problems of slow convergence rate, training instabilities, and unavailability of discrete data in traditional GAN, LDA-GAN utilizes the Gumbel-softmax technology to construct a differentiable process for simulating discrete sampling. Meanwhile, the generator and the discriminator of LDA-GAN are integrated to establish the overall optimization goal based on the pairwise loss function. Results: Experiments on standard datasets demonstrate that LDA-GAN achieves not only high stability and high efficiency in the process of confrontation learning but also gives full play to the semi-supervised learning advantage of generative adversarial learning framework for unlabeled data, which further improves the prediction accuracy of lncRNA-disease association. Besides, case studies show that LDA-GAN can accurately generate potential diseases for several lncRNAs. Conclusion: We introduce a generative adversarial model to identify lncRNA-disease associations.
引用
收藏
页码:144 / 151
页数:8
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