SpaNCMG: improving spatial domains identification of spatial transcriptomics using neighborhood-complementary mixed-view graph convolutional network

Author:

Si Zhihao1,Li Hanshuang23,Shang Wenjing1,Zhao Yanan1,Kong Lingjiao1,Long Chunshen23,Zuo Yongchun23ORCID,Feng Zhenxing1

Affiliation:

1. College of Sciences, Inner Mongolia University of Technology , Hohhot 010051 , China

2. State Key Laboratory of Reproductive Regulation and Breeding of Grassland Livestock , Institutes of Biomedical Sciences, College of Life Sciences, , Hohhot 010070 , China

3. Inner Mongolia University , Institutes of Biomedical Sciences, College of Life Sciences, , Hohhot 010070 , China

Abstract

Abstract The advancement of spatial transcriptomics (ST) technology contributes to a more profound comprehension of the spatial properties of gene expression within tissues. However, due to challenges of high dimensionality, pronounced noise and dynamic limitations in ST data, the integration of gene expression and spatial information to accurately identify spatial domains remains challenging. This paper proposes a SpaNCMG algorithm for the purpose of achieving precise spatial domain description and localization based on a neighborhood-complementary mixed-view graph convolutional network. The algorithm enables better adaptation to ST data at different resolutions by integrating the local information from KNN and the global structure from r-radius into a complementary neighborhood graph. It also introduces an attention mechanism to achieve adaptive fusion of different reconstructed expressions, and utilizes KPCA method for dimensionality reduction. The application of SpaNCMG on five datasets from four sequencing platforms demonstrates superior performance to eight existing advanced methods. Specifically, the algorithm achieved highest ARI accuracies of 0.63 and 0.52 on the datasets of the human dorsolateral prefrontal cortex and mouse somatosensory cortex, respectively. It accurately identified the spatial locations of marker genes in the mouse olfactory bulb tissue and inferred the biological functions of different regions. When handling larger datasets such as mouse embryos, the SpaNCMG not only identified the main tissue structures but also explored unlabeled domains. Overall, the good generalization ability and scalability of SpaNCMG make it an outstanding tool for understanding tissue structure and disease mechanisms. Our codes are available at https://github.com/ZhihaoSi/SpaNCMG.

Funder

Inner Mongolia of China

National Natural Science Foundation of Inner Mongolia University of Technology

Natural Scientific Foundation of China

Inner Mongolia Autonomous Region

College Student Innovation and Entrepreneurship Program

Publisher

Oxford University Press (OUP)

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