Affiliation:
1. College of Computer and Control Engineering, Northeast Forestry University , Harbin 150040 , China
2. Department of Obstetrics and Gynecology, the First Affiliated Hospital of Harbin Medical University , Harbin 150001 , China
Abstract
Abstract
With the emergence of spatial transcriptome sequencing (ST-seq), research now heavily relies on the joint analysis of ST-seq and single-cell RNA sequencing (scRNA-seq) data to precisely identify cell spatial composition in tissues. However, common methods for combining these datasets often merge data from multiple cells to generate pseudo-ST data, overlooking topological relationships and failing to represent spatial arrangements accurately. We introduce GTAD, a method utilizing the Graph Attention Network for deconvolution of integrated scRNA-seq and ST-seq data. GTAD effectively captures cell spatial relationships and topological structures within tissues using a graph-based approach, enhancing cell-type identification and our understanding of complex tissue cellular landscapes. By integrating scRNA-seq and ST data into a unified graph structure, GTAD outperforms traditional ‘pseudo-ST’ methods, providing robust and information-rich results. GTAD performs exceptionally well with synthesized spatial data and accurately identifies cell spatial composition in tissues like the mouse cerebral cortex, cerebellum, developing human heart and pancreatic ductal carcinoma. GTAD holds the potential to enhance our understanding of tissue microenvironments and cellular diversity in complex bio-logical systems. The source code is available at https://github.com/zzhjs/GTAD.
Funder
National Natural Science Foundation of China
Heilongjiang Postdoctoral Fund
Publisher
Oxford University Press (OUP)
Subject
Molecular Biology,Information Systems
Cited by
3 articles.
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