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首页> 外文期刊>IEEE Transactions on Circuits and Systems. I, Regular Papers >Nuclei Segmentation Using Marker-Controlled Watershed, Tracking Using Mean-Shift, and Kalman Filter in Time-Lapse Microscopy
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Nuclei Segmentation Using Marker-Controlled Watershed, Tracking Using Mean-Shift, and Kalman Filter in Time-Lapse Microscopy

机译:在时移显微镜中使用标记控制的分水岭进行核分割,使用均值漂移和卡尔曼滤波进行跟踪

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摘要

It is important to observe and study cancer cells' cycle progression in order to better understand drug effects on cancer cells. Time-lapse microscopy imaging serves as an important method to measure the cycle progression of individual cells in a large population. Since manual analysis is unreasonably time consuming for the large volumes of time-lapse image data, automated image analysis is proposed. Existing approaches dealing with time-lapse image data are rather limited and often give inaccurate analysis results, especially in segmenting and tracking individual cells in a cell population. In this paper, we present a new approach to segment and track cell nuclei in time-lapse fluorescence image sequence. First, we propose a novel marker-controlled watershed based on mathematical morphology, which can effectively segment clustered cells with less oversegmentation. To further segment undersegmented cells or to merge oversegmented cells, context information among neighboring frames is employed, which is proved to be an effective strategy. Then, we design a tracking method based on modified mean shift algorithm, in which several kernels with adaptive scale, shape, and direction are designed. Finally, we combine mean-shift and Kalman filter to achieve a more robust cell nuclei tracking method than existing ones. Experimental results show that our method can obtain 98.8% segmentation accuracy, 97.4% cell division tracking accuracy, and 97.6% cell tracking accuracy
机译:重要的是观察和研究癌细胞的循环进程,以便更好地了解药物对癌细胞的作用。延时显微镜成像是测量大量人群中单个细胞周期进程的重要方法。由于手动分析对于大量的延时图像数据不合理地耗时,因此提出了自动图像分析方法。现有的处理延时图像数据的方法相当有限,并且常常给出不准确的分析结果,尤其是在分割和跟踪细胞群中的单个细胞时。在本文中,我们提出了一种新的方法来分割和跟踪延时荧光图像序列中的细胞核。首先,我们提出了一种基于数学形态学的新型标记控制分水岭,该分水岭可以有效地分割簇状细胞,而避免过度分割。为了进一步分割分割不足的小区或合并分割过度的小区,采用了相邻帧之间的上下文信息,这被证明是一种有效的策略。然后,我们设计了一种基于改进的均值漂移算法的跟踪方法,在该方法中设计了具有自适应尺度,形状和方向的几个核。最后,我们结合均值漂移和卡尔曼滤波来实现比现有方法更健壮的细胞核跟踪方法。实验结果表明,该方法可以实现98.8%的分割精度,97.4%的细胞分裂跟踪精度和97.6%的细胞跟踪精度。

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