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 language | English (US) |
|---|---|
| Article number | 206 |
| Journal | Genome biology |
| Volume | 25 |
| Issue number | 1 |
| DOIs | |
| State | Published - 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