LETSmix: a spatially informed and learning-based domain adaptation method for cell-type deconvolution in spatial transcriptomics

Spatial transcriptomics (ST) has revolutionized our understanding of gene expression patterns by incorporating spatial context. However, many ST technologies operate on heterogeneous cell mixtures due to limited spatial resolution. To resolve cell type composition at each sequencing spot, several deconvolution methods have been proposed. Yet, these approaches often underutilize spatial context inherent in ST data and paired histopathological images, meanwhile overlooking domain variances between ST and reference single-cell RNA sequencing (scRNA-seq) data. Here, we present LETSmix, a novel deconvolution method that enhances spatial correlations within ST data using a tailored LETS filter, and employs a mixup-augmented domain adaptation strategy to address domain shifts. The performance of LETSmix was validated across diverse ST platforms and tissue types, including 10x Visium human dorsolateral prefrontal cortex, ST human pancreatic ductal adenocarcinoma, 10x Visium mouse liver, and Stereo-seq mouse olfactory bulb datasets. Our findings demonstrate that the proposed method accurately estimates cell type proportions and effectively maps them to the expected regions, establishing a new record among current state-of-the-art models. LETSmix is expected to serve as a robust tool for advancing studies on cellular composition and spatial architecture in spatial transcriptomics. GRAPHICAL ABSTRACT O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=149 SRC="FIGDIR/small/591425v2_ufig1.gif" ALT="Figure 1"> View larger version (35K): org.highwire.dtl.DTLVardef@1b264cborg.highwire.dtl.DTLVardef@f77e8forg.highwire.dtl.DTLVardef@9609ddorg.highwire.dtl.DTLVardef@61af58_HPS_FORMAT_FIGEXP M_FIG C_FIG