奇异值分解
计算机科学
相似性(几何)
图形
矩阵分解
环状RNA
算法
功能(生物学)
人工智能
理论计算机科学
小RNA
特征向量
生物
进化生物学
基因
图像(数学)
物理
量子力学
生物化学
作者
Yurong Qian,Jingjing Zheng,Zhe Zhang,Ying Jiang,Jiaxuan Zhang,Lei Deng
标识
DOI:10.1109/bibm52615.2021.9669875
摘要
A large amount of evidence shows that circular RNAs(circRNAs) participate in transcription and translation regulation and function as “micro RNA(miRNA)-sponges”. Recognizing circRNA-miRNA interaction is helpful to understand the function of circRNAs, especially its role in complex diseases. Obtaining interactive information based on traditional biological experiments is usually small-scale, time-consuming, and laborious. Considering that there are few calculation methods, it is urgent to develop efficient and accurate methods to extract the interaction between circRNA and miRNA. In this work, we proposed a computational framework called CMIVGSD, which uses singular value decomposition and graph variational auto-encoders to predict circRNA-miRNA interaction. To our best knowledge, CMIVGSD is the first calculation framework to predict circRNA-miRNA interaction. CMIVGSD uses the singular value decomposition (SVD) algorithm to obtain linear features from the circRNA-miRNA interaction matrix. We have constructed the similarity networks of circRNA and miRNA, respectively. The graph variational auto-encoder (VGAE) is employed to mine the non-linear features of circRNA-miRNA in similarity networks. Finally, we combine linear and non-linear features and use LightGBM to predict interaction scores. We performed five-fold cross-validation experiments. Experimental results show that our proposed method is better than other methods. The case study further proves the effectiveness of CMIVGSD in predicting circRNA-miRNA interaction.
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