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 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.
翻译:细胞跟踪是确定单细胞特征的基本工具,如分裂模式或延长率等。 与常见的多对象跟踪不同,微生物活细胞实验细胞在逐渐增长、移动和分化,形成一个密集的单层结构中的细胞聚集点。随着细胞数量不断增加,在几代人中正确遵循精确的细胞协会之后,由于可能的协会数目大量增加,许多代代代代都越来越具有挑战性。为了应对这一挑战,我们建议采用一个快速无参数的细胞跟踪方法,其中包括将生长的细胞和组合式解析器作为活动优先对象,分配给女儿分解母细胞。作为跟踪的投入,Omnition用于实例分割。与传统的近邻跟踪方法不同,我们拟议方法的分派步骤基于一个基于高斯活动的标准,预测特定细胞迁移的概率,从而限制错误分配的次数。除了作为细胞跟踪的建筑块外,拟议的活动地图是用来说明其女儿的母细胞分离细胞细胞的分解的分解的测量器。最后,我们进行一个用于跟踪其细胞生长结果的量化框架,用于跟踪其正确度的实验。