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Heterogeneity Mapping of Protein Expression in Tumors using Quantitative Immunofluorescence
Published on: October 25, 2011
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Semi-automated approaches for interrogating spatial heterogeneity of tissue samples
Vytautas Navikas1, Joanna Kowal1, Daniel Rodriguez1
1Lunaphore Technologies SA, Tolochenaz, Switzerland.
Scientific Reports
|February 29, 2024
Summary
Spatial biology tools enable semi-automated analysis of multiplex whole-tissue images for understanding tissue composition. This approach facilitates single-cell resolution exploration of the tumor microenvironment (TME) with a user-friendly workflow.
Area of Science:
- Spatial biology
- Biomedical imaging
- Computational pathology
Background:
- Tissues are complex ecosystems where cellular interactions drive biological processes and disease.
- Understanding tissue composition at single-cell resolution is crucial for biological and medical insights.
- Multiplex whole-tissue imaging generates large datasets requiring advanced analytical methods.
Purpose of the Study:
- To present a semi-automated workflow for analyzing multiplex whole-tissue images.
- To demonstrate the utility of open-source tools for spatial biology data extraction.
- To facilitate the exploration of tumor microenvironment (TME) composition at single-cell resolution.
Main Methods:
- Utilized the Lunaphore COMET platform for interrogating lung cancer specimens with 20 biomarkers.
- Employed an in-house optimized nuclei detection algorithm and a novel image artifact exclusion approach.
- Processed data using publicly available image analysis frameworks to ensure compatibility.
Main Results:
- Demonstrated a semi-automated workflow for multiplex whole-tissue image analysis.
- Showcased the compatibility of COMET-derived data with existing analysis frameworks.
- Enabled single-cell resolution spatial cellular dissection of tissue composition.
Conclusions:
- The presented workflow offers an accessible, slide-in, data-out approach for multiplex imaging analysis.
- This method simplifies the exploration of TME composition at single-cell resolution.
- The workflow is transferable to diverse specimen cohorts, providing a valuable toolset for spatial biology research.
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