DCDA: CircRNA-Disease Association Prediction with Feed-Forward Neural Network and Deep Autoencoder

被引:3
作者
Turgut, Hacer [1 ]
Turanli, Beste [2 ]
Boz, Betuel [1 ]
机构
[1] Marmara Univ, Dept Comp Engn, TR-34854 Istanbul, Turkiye
[2] Marmara Univ, Dept Bioengn, TR-34854 Istanbul, Turkiye
关键词
CircRNA; CircRNA-disease association; Deep learning; Autoencoder; Neural network; CIRCULAR RNA;
D O I
10.1007/s12539-023-00590-y
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Circular RNA is a single-stranded RNA with a closed-loop structure. In recent years, academic research has revealed that circular RNAs play critical roles in biological processes and are related to human diseases. The discovery of potential circRNAs as disease biomarkers and drug targets is crucial since it can help diagnose diseases in the early stages and be used to treat people. However, in conventional experimental methods, conducting experiments to detect associations between circular RNAs and diseases is time-consuming and costly. To overcome this problem, various computational methodologies are proposed to extract essential features for both circular RNAs and diseases and predict the associations. Studies showed that computational methods successfully predicted performance and made it possible to detect possible highly related circular RNAs for diseases. This study proposes a deep learning-based circRNA-disease association predictor methodology called DCDA, which uses multiple data sources to create circRNA and disease features and reveal hidden feature codings of a circular RNA-disease pair with a deep autoencoder, then predict the relation score of the pair by a deep neural network. Fivefold cross-validation results on the benchmark dataset showed that our model outperforms state-of-the-art prediction methods in the literature with the AUC score of 0.9794.
引用
收藏
页码:91 / 103
页数:13
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