Abstract

BackgroundAlgorithmic cellular segmentation is an essential step for the quantitative analysis of highly multiplexed tissue images. Current segmentation pipelines often require manual dataset annotation and additional training, significant parameter tuning, or a sophisticated understanding of programming to adapt the software to the researcher’s need. Here, we present CellSeg, an open-source, pre-trained nucleus segmentation and signal quantification software based on the Mask region-convolutional neural network (R-CNN) architecture. CellSeg is accessible to users with a wide range of programming skills.ResultsCellSeg performs at the level of top segmentation algorithms in the 2018 Kaggle Data Challenge both qualitatively and quantitatively and generalizes well to a diverse set of multiplexed imaged cancer tissues compared to established state-of-the-art segmentation algorithms. Automated segmentation post-processing steps in the CellSeg pipeline improve the resolution of immune cell populations for downstream single-cell analysis. Finally, an application of CellSeg to a highly multiplexed colorectal cancer dataset acquired on the CO-Detection by indEXing (CODEX) platform demonstrates that CellSeg can be integrated into a multiplexed tissue imaging pipeline and lead to accurate identification of validated cell populations.ConclusionCellSeg is a robust cell segmentation software for analyzing highly multiplexed tissue images, accessible to biology researchers of any programming skill level.

Highlights

  • Tissue imaging and single-cell analysis can reveal previously undetected biological structure and uncover subtle spatial relationships between cells

  • CellSeg architecture achieves high performance on Kaggle data challenge test set After implementing CellSeg, we validated each step of the pipeline: architecture, segmentation, segmentation post-processing, and output

  • CellSeg was tested for segmentation quality on a ground truth segmented validation set of 3717 nuclei from Kaggle (Fig. 2A)

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Summary

Introduction

Tissue imaging and single-cell analysis can reveal previously undetected biological structure and uncover subtle spatial relationships between cells. Lee et al BMC Bioinformatics (2022) 23:46 interactions between tumor, immune and stromal cells, and healthy host tissue [10,11,12,13,14,15,16] In such highly multiplexed tissue imaging studies, the quality and accuracy of downstream analyses depend critically on the precise identification and correct phenotypic assignment of single cells, which requires accurate demarcation of each cell’s boundary and quantification of its marker expression. This is usually accomplished using an automated segmentation and signal quantification algorithm [17]. CellSeg is accessible to users with a wide range of programming skills

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