OpenIMC: an open-source platform for analyzing single-cell and spatial proteomics by imaging mass cytometry

BACKGROUND: Imaging Mass Cytometry (IMC) enables highly multiplexed, spatially resolved single-cell proteomics, providing simultaneous measurement of dozens of protein markers while preserving tissue architecture. Despite its analytical power, IMC data analysis remains fragmented across multiple software environments, requiring researchers to combine independent tools for visualization, preprocessing, segmentation, feature extraction, phenotyping, batch correction, and spatial analysis. This fragmentation increases technical barriers, complicates reproducibility, and limits accessibility for non-computational users. RESULTS: We developed OpenIMC, an open-source platform that integrates the major stages of IMC analysis within a unified graphical and command-line framework. OpenIMC supports image visualization, quality control, preprocessing, segmentation, feature extraction, dimensionality reduction, batch effect correction, clustering, phenotyping, and spatial analysis while maintaining interoperability with established community tools. The platform incorporates automated provenance tracking, records analytical parameters and software versions, and enables export and sharing of complete analytical sessions. Benchmarking demonstrated deterministic behavior across repeated runs, complete concordance between graphical and command-line workflows, and strong agreement with established IMC analysis pipelines. OpenIMC additionally provides support for high-resolution IMC workflows, including signal attenuation modeling and image deconvolution. We apply OpenIMC to two datasets of circulating cells and breast tissue to demonstrate the platform's ability to support integrated single-cell and spatial proteomics analysis. CONCLUSIONS: OpenIMC reduces the complexity of IMC data analysis by providing a unified, reproducible, and extensible framework for common IMC workflows. By combining interactive visualization with scalable computational analysis, OpenIMC lowers technical barriers and facilitates reproducible single-cell and spatial proteomics research.

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Publication Details

Journal
BMC Bioinformatics
Published
2026-06-30
DOI
https://doi.org/10.1186/s12859-026-06547-4
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
0.00

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article

OpenIMC: an open-source platform for analyzing single-cell and spatial proteomics by imaging mass cytometry

Peter Kühn, Valerie Hennes, E. Shelley Hwang, James Hicks et al.
BMC Bioinformatics
Single-cell and spatial transcriptomics
article

OpenIMC: an open-source platform for analyzing single-cell and spatial proteomics by imaging mass cytometry

Peter Kühn, Valerie Hennes, E. Shelley Hwang, James Hicks, Dean Tessone, Jorge Nieva, Mohamed Kamal, Ahmed H. Saadawy
article en

Abstract

BACKGROUND: Imaging Mass Cytometry (IMC) enables highly multiplexed, spatially resolved single-cell proteomics, providing simultaneous measurement of dozens of protein markers while preserving tissue architecture. Despite its analytical power, IMC data analysis remains fragmented across multiple software environments, requiring researchers to combine independent tools for visualization, preprocessing, segmentation, feature extraction, phenotyping, batch correction, and spatial analysis. This fragmentation increases technical barriers, complicates reproducibility, and limits accessibility for non-computational users. RESULTS: We developed OpenIMC, an open-source platform that integrates the major stages of IMC analysis within a unified graphical and command-line framework. OpenIMC supports image visualization, quality control, preprocessing, segmentation, feature extraction, dimensionality reduction, batch effect correction, clustering, phenotyping, and spatial analysis while maintaining interoperability with established community tools. The platform incorporates automated provenance tracking, records analytical parameters and software versions, and enables export and sharing of complete analytical sessions. Benchmarking demonstrated deterministic behavior across repeated runs, complete concordance between graphical and command-line workflows, and strong agreement with established IMC analysis pipelines. OpenIMC additionally provides support for high-resolution IMC workflows, including signal attenuation modeling and image deconvolution. We apply OpenIMC to two datasets of circulating cells and breast tissue to demonstrate the platform's ability to support integrated single-cell and spatial proteomics analysis. CONCLUSIONS: OpenIMC reduces the complexity of IMC data analysis by providing a unified, reproducible, and extensible framework for common IMC workflows. By combining interactive visualization with scalable computational analysis, OpenIMC lowers technical barriers and facilitates reproducible single-cell and spatial proteomics research.

BMC Bioinformatics
University of Southern California (US), Duke University (US), USC Norris Comprehensive Cancer Center (US), Convergent Science (United States) (US)
Breast Cancer Research Foundation, Dr. Miriam and Sheldon G. Adelson Medical Research Foundation, USC Norris Comprehensive Cancer Center
Partnerships for the goals
Openalex Percentile: Top 12%
Single-cell and spatial transcriptomics
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