STdGCN: spatial transcriptomic cell-type deconvolution using graph convolutional networks

Yawei Li, Yuan Luo*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

14 Scopus citations

Abstract

Spatially resolved transcriptomics integrates high-throughput transcriptome measurements with preserved spatial cellular organization information. However, many technologies cannot reach single-cell resolution. We present STdGCN, a graph model leveraging single-cell RNA sequencing (scRNA-seq) as reference for cell-type deconvolution in spatial transcriptomic (ST) data. STdGCN incorporates expression profiles from scRNA-seq and spatial localization from ST data for deconvolution. Extensive benchmarking on multiple datasets demonstrates that STdGCN outperforms 17 state-of-the-art models. In a human breast cancer Visium dataset, STdGCN delineates stroma, lymphocytes, and cancer cells, aiding tumor microenvironment analysis. In human heart ST data, STdGCN identifies changes in endothelial-cardiomyocyte communications during tissue development.

Original languageEnglish (US)
Article number206
JournalGenome biology
Volume25
Issue number1
DOIs
StatePublished - Dec 2024

Funding

This study is supported in part by NIH grant U01TR003528, 1R01LM013337.

Keywords

  • Cell-type deconvolution
  • Deep learning
  • Graph convolutional networks
  • Spatial transcriptomics

ASJC Scopus subject areas

  • Ecology, Evolution, Behavior and Systematics
  • Genetics
  • Cell Biology

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