bioRxiv · 10.64898/2026.08.24.746722
SCORPy: Lowering the computational barrier to reproducible multiplexed imaging spatial single cell proteomics analysis
Abstract
Spatially resolved single-cell proteomic imaging technologies, including cyclic immunofluorescence (CycIF), generate high-dimensional data, critical for tissue-scale biological analysis. However, single-cell analysis remains computationally demanding, lacks standardization across platforms and is often inaccessible to experimental biologists without programming expertise. Here we present SCORPy (Single-Cell proteOmics Research Platform), a standalone, cross-platform desktop application that provides an end-to-end, code-free workflow for the analysis of single-cell proteomic data extracted from imaging experiments. SCORPy introduces methodological advances for preprocessing multiplexed imaging data: an exposure-aware, cycle-matched background correction strategy, and a normalization framework that harmonizes signal distributions across markers while enabling batch correction across experiments. These approaches are integrated with quality control, interactive thresholding and cell phenotyping using a hierarchical cell reference library, and downstream compositional and spatial analyses within a unified interface. Sample-level metadata can be incorporated throughout the workflow to support integrative analyses and facilitate generation of publication-ready visualizations. By combining robust preprocessing methods with an accessible implementation, SCORPy reduces computational barriers and promotes broader adoption of spatial single-cell proteomics analysis.
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Gerber, Z., Simard, S., Kolipaka, H., Drouin, Z., Sevigny, J., Pourcel, V., del Carmen Crespo Oliva, C., Tate, B., Mouzakitis, K., Placet, M., Jean, D., Deuel, K., Pavlatos, E., Sturgill, E., Pucilowska, J., Mills, G. B., Labrie, M.. 2026-08-25. SCORPy: Lowering the computational barrier to reproducible multiplexed imaging spatial single cell proteomics analysis. https://doi.org/10.64898/2026.08.24.746722
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