Method

Flexible and scalable inference of spatially varying correlation in spatial transcriptomics with spCorr

    • 1Department of Statistics and Data Science, University of California, Los Angeles, California 90095, USA;
    • 2Department of Genetics and Genome Sciences, University of Connecticut Health Center, Farmington, Connecticut 06030, USA;
    • 3The Jackson Laboratory for Genomic Medicine, Farmington, Connecticut 06032, USA;
    • 4Institute for Systems Genomics, University of Connecticut, Farmington, Connecticut 06030, USA;
    • 5Biostatistics Program, Public Health Science Division, Fred Hutchinson Cancer Center, Seattle, Washington 98109, USA;
    • 6Department of Biostatistics, University of Washington, Seattle, Washington 98195, USA;
    • 7Department of Statistics, University of Washington, Seattle, Washington 98195, USA;
    • 8Department of Genome Sciences, University of Washington, Seattle, Washington 98195, USA
Published June 17, 2026. https://doi.org/10.1101/gr.281559.125
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Abstract

Spatial transcriptomics has transformed our ability to explore gene expression within its tissue context, enabling us to dissect subtle yet biologically significant variations in situ. Although numerous computational methods have been proposed to identify Spatially Varying Genes (SVGs) by modeling their expression separately, much less effort has been devoted to understanding how correlations between genes change across space. Such Spatially Varying Correlations (SVCs) are critical for understanding biological processes such as gene regulatory mechanisms shaped by local tissue environments, yet existing tools remain limited for this task. To address this gap, we present spCorr, a flexible and scalable regression framework for studying SVCs. spCorr provides interpretable, spot-level estimates of gene correlation and detects gene pairs whose correlations vary across locations or between tissue domains. Through extensive simulations and real-data analyses, we show that spCorr achieves high detection power, reliably controls the False Discovery Rate (FDR), and is computationally efficient. Importantly, spCorr reveals biologically meaningful correlation patterns that highlight fine-scale tissue structures, gene module functions, and region-specific interactions, offering new opportunities to study coordinated gene regulation in spatial transcriptomics.

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