Cell tracking for live-cell microscopy using an activity-prioritized assignment strategy

Karina Ruzaeva, J. Cohrs, Keitaro Kasahara, D. Kohlheyer, K. Nöh, B. Berkels
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引用次数: 2

Abstract

Cell tracking is an essential tool in live-cell imaging to determine single-cell features, such as division patterns or elongation rates. Unlike in common multiple object tracking, in microbial live-cell experiments cells are growing, moving, and dividing over time, to form cell colonies that are densely packed in mono-layer structures. With increasing cell numbers, following the precise cell-cell associations correctly over many generations becomes more and more challenging, due to the massively increasing number of possible associations. To tackle this challenge, we propose a fast parameter-free cell tracking approach, which consists of activity-prioritized nearest neighbor assignment of growing (expanding) cells and a combinatorial solver that assigns splitting mother cells to their daughters. As input for the tracking, Omnipose is utilized for instance segmentation. Unlike conventional nearest-neighbor-based tracking approaches, the assignment steps of our proposed method are based on a Gaussian activity-based metric, predicting the cell-specific migration probability, thereby limiting the number of erroneous assignments. In addition to being a building block for cell tracking, the proposed activity map is a standalone tracking-free metric for indicating cell activity. Finally, we perform a quantitative analysis of the tracking accuracy for different frame rates, to inform life scientists about a suitable (in terms of tracking performance) choice of the frame rate for their cultivation experiments, when cell tracks are the desired key outcome.
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使用活动优先分配策略的活细胞显微镜细胞跟踪
细胞跟踪是活细胞成像中确定单细胞特征(如分裂模式或延伸率)的重要工具。与常见的多目标跟踪不同,在微生物活细胞实验中,细胞随着时间的推移生长、移动和分裂,形成细胞菌落,这些菌落密集地排列在单层结构中。随着细胞数量的增加,由于可能的关联数量大量增加,在许多代中正确地跟踪精确的细胞-细胞关联变得越来越具有挑战性。为了解决这一挑战,我们提出了一种快速无参数细胞跟踪方法,该方法由生长(扩展)细胞的活性优先近邻分配和将分裂母细胞分配给其子细胞的组合求解器组成。作为跟踪的输入,Omnipose被用于实例分割。与传统的基于最近邻的跟踪方法不同,我们提出的方法的分配步骤是基于基于高斯活动的度量,预测细胞特异性迁移概率,从而限制错误分配的数量。除了作为细胞跟踪的构建块之外,所建议的活动映射还是一个独立的无跟踪度量,用于指示细胞活动。最后,我们对不同帧率的跟踪精度进行了定量分析,以告知生命科学家在他们的培养实验中选择合适的帧率(就跟踪性能而言),当细胞轨迹是期望的关键结果时。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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