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A graph-based cell tracking algorithm with few manually tunable parameters and automated segmentation error correction

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  • Katharina Löffler
  • Tim Scherr
  • Ralf Mikut

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.

Suggested Citation

  • Katharina Löffler & Tim Scherr & Ralf Mikut, 2021. "A graph-based cell tracking algorithm with few manually tunable parameters and automated segmentation error correction," PLOS ONE, Public Library of Science, vol. 16(9), pages 1-28, September.
  • Handle: RePEc:plo:pone00:0249257
    DOI: 10.1371/journal.pone.0249257
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    References listed on IDEAS

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    1. Tim Scherr & Katharina Löffler & Moritz Böhland & Ralf Mikut, 2020. "Cell segmentation and tracking using CNN-based distance predictions and a graph-based matching strategy," PLOS ONE, Public Library of Science, vol. 15(12), pages 1-22, December.
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    Cited by:

    1. Sean M. Gross & Farnaz Mohammadi & Crystal Sanchez-Aguila & Paulina J. Zhan & Tiera A. Liby & Mark A. Dane & Aaron S. Meyer & Laura M. Heiser, 2023. "Analysis and modeling of cancer drug responses using cell cycle phase-specific rate effects," Nature Communications, Nature, vol. 14(1), pages 1-12, December.
    2. Szimonetta Xénia Tamás & Benoit Thomas Roux & Boldizsár Vámosi & Fabian Gregor Dehne & Anna Török & László Fazekas & Balázs Enyedi, 2023. "A genetically encoded sensor for visualizing leukotriene B4 gradients in vivo," Nature Communications, Nature, vol. 14(1), pages 1-11, December.

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