stAA: adversarial graph autoencoder for spatial clustering task of spatially resolved transcriptomics

被引:3
|
作者
Fang, Zhaoyu [1 ]
Liu, Teng [2 ]
Zheng, Ruiqing [1 ]
Jin, A.
Yin, Mingzhu [2 ]
Li, Min [1 ]
机构
[1] Cent South Univ, Sch Comp Sci & Engn, Changsha 410083, Hunan, Peoples R China
[2] Chongqing Univ, Gorges Hosp 3, Med Pathol Ctr MPC, Clin Res Ctr CRC,Canc Early Detect & Treatment Ctr, Chongqing 404031, Peoples R China
基金
中国国家自然科学基金;
关键词
spatial transcriptomics; spatial domain; graph neural network; adversarial learning; graph autoencoder; GENOME-WIDE EXPRESSION; ATLAS;
D O I
10.1093/bib/bbad500
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
With the development of spatially resolved transcriptomics technologies, it is now possible to explore the gene expression profiles of single cells while preserving their spatial context. Spatial clustering plays a key role in spatial transcriptome data analysis. In the past 2 years, several graph neural network-based methods have emerged, which significantly improved the accuracy of spatial clustering. However, accurately identifying the boundaries of spatial domains remains a challenging task. In this article, we propose stAA, an adversarial variational graph autoencoder, to identify spatial domain. stAA generates cell embedding by leveraging gene expression and spatial information using graph neural networks and enforces the distribution of cell embeddings to a prior distribution through Wasserstein distance. The adversarial training process can make cell embeddings better capture spatial domain information and more robust. Moreover, stAA incorporates global graph information into cell embeddings using labels generated by pre-clustering. Our experimental results show that stAA outperforms the state-of-the-art methods and achieves better clustering results across different profiling platforms and various resolutions. We also conducted numerous biological analyses and found that stAA can identify fine-grained structures in tissues, recognize different functional subtypes within tumors and accurately identify developmental trajectories.
引用
收藏
页数:12
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