A multi-modality and multi-granularity collaborative learning framework for identifying spatial domains and spatially variable genes

Abstract Motivation Recent advances in spatial transcriptomics technologies have provided multi-modality data integrating gene expression, spatial context, and histological images. Accurately identifying spatial domains and spatially variable genes is crucial for understanding tissue structures and...

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Veröffentlicht in:Bioinformatics (Oxford, England) England), 2024-10, Vol.40 (10)
Hauptverfasser: Liang, Xiao, Liu, Pei, Xue, Li, Chen, Baiyun, Liu, Wei, Shi, Wanwan, Wang, Yongwang, Chen, Xiangtao, Luo, Jiawei
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Sprache:eng
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Zusammenfassung:Abstract Motivation Recent advances in spatial transcriptomics technologies have provided multi-modality data integrating gene expression, spatial context, and histological images. Accurately identifying spatial domains and spatially variable genes is crucial for understanding tissue structures and biological functions. However, effectively combining multi-modality data to identify spatial domains and determining SVGs closely related to these spatial domains remains a challenge. Results In this study, we propose spatial transcriptomics multi-modality and multi-granularity collaborative learning (spaMMCL). For detecting spatial domains, spaMMCL mitigates the adverse effects of modality bias by masking portions of gene expression data, integrates gene and image features using a shared graph convolutional network, and employs graph self-supervised learning to deal with noise from feature fusion. Simultaneously, based on the identified spatial domains, spaMMCL integrates various strategies to detect potential SVGs at different granularities, enhancing their reliability and biological significance. Experimental results demonstrate that spaMMCL substantially improves the identification of spatial domains and SVGs. Availability and implementation The code and data of spaMMCL are available on Github: Https://github.com/liangxiao-cs/spaMMCL.
ISSN:1367-4811
1367-4803
1367-4811
DOI:10.1093/bioinformatics/btae607