自编码
人工智能
核(代数)
深度学习
相似性(几何)
计算机科学
特征学习
多核学习
代表(政治)
机器学习
特征(语言学)
模式识别(心理学)
核方法
支持向量机
数学
法学
组合数学
哲学
图像(数学)
政治
语言学
政治学
作者
Feng Zhou,Meng-Meng Yin,Cui-Na Jiao,Jing-Xiu Zhao,Chun-Hou Zheng,Jin‐Xing Liu
出处
期刊:IEEE transactions on neural networks and learning systems
[Institute of Electrical and Electronics Engineers]
日期:2021-12-03
卷期号:34 (9): 5570-5579
被引量:20
标识
DOI:10.1109/tnnls.2021.3129772
摘要
Determining microRNA (miRNA)-disease associations (MDAs) is an integral part in the prevention, diagnosis, and treatment of complex diseases. However, wet experiments to discern MDAs are inefficient and expensive. Hence, the development of reliable and efficient data integrative models for predicting MDAs is of significant meaning. In the present work, a novel deep learning method for predicting MDAs through deep autoencoder with multiple kernel learning (DAEMKL) is presented. Above all, DAEMKL applies multiple kernel learning (MKL) in miRNA space and disease space to construct miRNA similarity network and disease similarity network, respectively. Then, for each disease or miRNA, its feature representation is learned from the miRNA similarity network and disease similarity network via the regression model. After that, the integrated miRNA feature representation and disease feature representation are input into deep autoencoder (DAE). Furthermore, the novel MDAs are predicted through reconstruction error. Ultimately, the AUC results show that DAEMKL achieves outstanding performance. In addition, case studies of three complex diseases further prove that DAEMKL has excellent predictive performance and can discover a large number of underlying MDAs. On the whole, our method DAEMKL is an effective method to identify MDAs.
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