Abstract

Automatic cell segmentation and tracking enables to gain quantitative insights into the processes driving cell migration. To investigate new data with minimal manual effort, cell tracking algorithms should be easy to apply and reduce manual curation time by providing automatic correction of segmentation errors. Current cell tracking algorithms, however, are either easy to apply to new data sets but lack automatic segmentation error correction, or have a vast set of parameters that needs either manual tuning or annotated data for parameter tuning. In this work, we propose a tracking algorithm with only few manually tunable parameters and automatic segmentation error correction. Moreover, no training data is needed. We compare the performance of our approach to three well-performing tracking algorithms from the Cell Tracking Challenge on data sets with simulated, degraded segmentation-including false negatives, over- and under-segmentation errors. Our tracking algorithm can correct false negatives, over- and under-segmentation errors as well as a mixture of the aforementioned segmentation errors. On data sets with under-segmentation errors or a mixture of segmentation errors our approach performs best. Moreover, without requiring additional manual tuning, our approach ranks several times in the top 3 on the 6th edition of the Cell Tracking Challenge.

Highlights

  • The ability of cells to migrate is essential for many biological processes such as tissue formation, immune response, or wound healing [1]

  • The main contributions are: a) We propose a tracking approach able to handle the segmentation errors under- and over-segmentation with more than two objects involved and False Negatives (FN). b) We make our Python code available as open source https://git.scc.kit.edu/KIT-Sch-GE/ 2021-cell-tracking. c) We compare our tracking approach to three other tracking approaches which performed competitive on the Cell Tracking Challenge (CTC) http:// celltrackingchallenge.net/ [5, 50] and investigate how robust the selected tracking approaches perform, when the segmentation quality decreases. d) We show that our tracking algorithm performs well on a vast set of 2D and 3D data sets of the CTC using the same parametrization of our manually tunable parameters for all data sets

  • We investigate the influence of the post-processing steps, untangling tracks and FN correction, by modifying the post-processing step, while keeping all other steps the same

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Summary

Introduction

The ability of cells to migrate is essential for many biological processes such as tissue formation, immune response, or wound healing [1]. Disruptions in cell migration can contribute to diseases such as malformation [2], autoimmune disease [3], and metastasis [4]. To better understand the mechanisms driving cell migration, the cell behavior can be analyzed quantitatively, for instance by tracking cells over time. Tracking cells manually is tedious, even for small data sets, and becomes for large data sets infeasible. Automated cell tracking methods are needed which minimize manual curation effort and expert knowledge for parameter adjustments.

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