GLAE: A graph-learnable auto-encoder for single-cell RNA-seq analysis

被引:6
作者
Shan, Yixiang [1 ]
Yang, Jielong [1 ]
Li, Xiangtao [1 ]
Zhong, Xionghu [2 ]
Chang, Yi [1 ]
机构
[1] Jilin Univ, Sch Artificial Intelligence, Changchun 130012, Jilin Province, Peoples R China
[2] Hunan Univ, Coll Comp Sci & Elect Engn, Changsha 410082, Hunan Province, Peoples R China
基金
中国国家自然科学基金;
关键词
ScRNA analysing; Clustering; Auto; -encoder; Cell relation graph learning; Graph neural networks; DIVERSITY;
D O I
10.1016/j.ins.2022.11.049
中图分类号
TP [自动化技术、计算机技术];
学科分类号
0812 ;
摘要
Single-cell RNA sequencing (scRNA-seq) methods based on graph neural networks (GNNs) can make good use of cell relation graphs. Considering the cell relation graph is unknown in most situations, some GNN-based methods generate a pre-fixed cell relation graph using all the features (i.e., genes) from a single perspective and input it into GNN models. However, these GNN-based models can be severely hurt by the pre-fixed relation graph especially when it is not well pre-obtained due to the scRNA-seq errors. In addition, such methods learn the cell relation graph from a single perspective using all the features, which ignores the different influences of different gene subsets on cell relations. In this paper, we propose a novel end-to-end GNN-based scRNA-seq method called GLAE to address the above shortcomings, which is capable of learning cell relation graphs from different perspectives adaptively during the training process. We compare GLAE with several recently proposed methods and the results on six scRNA-seq datasets show that GLAE outperforms most of the methods on clustering tasks and is able to learn a meaningful cell relation graph for downstream tasks. (c) 2022 Elsevier Inc. All rights reserved.
引用
收藏
页码:88 / 103
页数:16
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