Inferring gene regulatory networks from single-cell transcriptomics based on graph embedding

被引:2
|
作者
Gan, Yanglan [1 ]
Yu, Jiacheng [1 ]
Xu, Guangwei [1 ]
Yan, Cairong [1 ]
Zou, Guobing [2 ]
机构
[1] Donghua Univ, Sch Comp Sci & Technol, Shanghai 201620, Peoples R China
[2] Shanghai Univ, Sch Comp Engn & Sci, Shanghai 200444, Peoples R China
基金
中国国家自然科学基金;
关键词
EXPRESSION; CIRCUITRY;
D O I
10.1093/bioinformatics/btae291
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation Gene regulatory networks (GRNs) encode gene regulation in living organisms, and have become a critical tool to understand complex biological processes. However, due to the dynamic and complex nature of gene regulation, inferring GRNs from scRNA-seq data is still a challenging task. Existing computational methods usually focus on the close connections between genes, and ignore the global structure and distal regulatory relationships.Results In this study, we develop a supervised deep learning framework, IGEGRNS, to infer GRNs from scRNA-seq data based on graph embedding. In the framework, contextual information of genes is captured by GraphSAGE, which aggregates gene features and neighborhood structures to generate low-dimensional embedding for genes. Then, the k most influential nodes in the whole graph are filtered through Top-k pooling. Finally, potential regulatory relationships between genes are predicted by stacking CNNs. Compared with nine competing supervised and unsupervised methods, our method achieves better performance on six time-series scRNA-seq datasets.Availability and implementation Our method IGEGRNS is implemented in Python using the Pytorch machine learning library, and it is freely available at https://github.com/DHUDBlab/IGEGRNS.
引用
收藏
页数:9
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