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Siamese Tracking of Cell Behaviour Patterns

机译:暹罗追踪细胞行为模式

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Tracking and segmentation of biological cells in video sequences is a challenging problem, especially due to the similarity of the cells and high levels of inherent noise. Most machine learning-based approaches lack robustness and suffer from sensitivity to less prominent events such as mitosis, apoptosis and cell collisions. Due to the large variance in medical image characteristics, most approaches are dataset-specific and do not generalise well on other datasets. In this paper, we propose a simple end-to-end cascade neural architecture that can effectively model the movement behaviour of biological cells and predict collision and mitosis events. Our approach uses U-Net for an initial segmentation which is then improved through processing by a siamese tracker capable of matching each cell along the temporal axis. By facilitating the re-segmentation of collided and mitotic cells, our method demonstrates its capability to handle volatile trajectories and unpredictable cell locations while being invariant to cell morphology. We demonstrate that our tracking approach achieves state-of-the-art results on PhC-C2DL-PSC and Fluo-N2DH-SIM+ datasets and ranks second on the DIC-C2DH-HeLa dataset of the cell tracking challenge benchmarks.
机译:视频序列中生物细胞的跟踪和分割是一个具有挑战性的问题,尤其是由于细胞的相似性和高水平的固有噪声。大多数基于机器的学习方法缺乏鲁棒性,并且对诸如有丝分裂,细胞凋亡和细胞碰撞等较少突出事件的敏感性缺乏敏感性。由于医学图像特征的差异,大多数方法是特定于数据集的,并且在其他数据集上不概括。在本文中,我们提出了一种简单的端到端级联神经结构,可以有效地模拟生物细胞的运动行为和预测碰撞和有丝分裂事件。我们的方法使用U-Net进行初始分割,然后通过能够匹配沿时间轴匹配每个小区的暹罗跟踪器来改善。通过促进碰撞和有丝分裂细胞的重新分割,我们的方法证明了其能力处理挥发性轨迹和不可预测的细胞位置,同时不变于细胞形态。我们证明,我们的跟踪方法在PHC-C2DL-PSC和Fluo-N2DH-SIM +数据集上实现了最先进的结果,并在单元格跟踪挑战基准的DIC-C2DH-HELA数据集中排名第二。

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