Spatial-ID: a cell typing method for spatially resolved transcriptomics via transfer learning and spatial embedding

Rongbo Shen(Tencent (China)), Lin Liu(BGI Group (China)), Zihan Wu(Tencent (China)), Ying Zhang(BGI Group (China)), Zhiyuan Yuan(Tencent (China)), Junfu Guo(BGI Group (China)), Fan Yang(Tencent (China)), Chao Zhang(BGI Group (China)), Bichao Chen(BGI Group (China)), Wanwan Feng(Tencent (China)), Chao Liu(BGI Group (China)), Jing Guo(BGI Group (China)), Guozhen Fan(BGI Group (China)), Yong Zhang(BGI Group (China)), Yuxiang Li(BGI Group (China)), Xun Xu(BGI Group (China)), Jianhua Yao(Tencent (China))
Nature Communications
December 10, 2022
Cited by 77Open Access
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Abstract

Spatially resolved transcriptomics provides the opportunity to investigate the gene expression profiles and the spatial context of cells in naive state, but at low transcript detection sensitivity or with limited gene throughput. Comprehensive annotating of cell types in spatially resolved transcriptomics to understand biological processes at the single cell level remains challenging. Here we propose Spatial-ID, a supervision-based cell typing method, that combines the existing knowledge of reference single-cell RNA-seq data and the spatial information of spatially resolved transcriptomics data. We present a series of benchmarking analyses on publicly available spatially resolved transcriptomics datasets, that demonstrate the superiority of Spatial-ID compared with state-of-the-art methods. Besides, we apply Spatial-ID on a self-collected mouse brain hemisphere dataset measured by Stereo-seq, that shows the scalability of Spatial-ID to three-dimensional large field tissues with subcellular spatial resolution.


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