半监督3D神经网络在无标记相位对比时间序列图像中跟踪iPS细胞分裂

A. Peskin, J. Chalfoun, M. Halter, A. Plant
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引用次数: 1

摘要

为了预测细胞群体的行为,了解单个细胞的动态特性是很重要的。在很长一段时间内,单个诱导多能干细胞(iPS)在集落中很难追踪,因为细胞的距离很近,分割是具有挑战性的,因为细胞分裂时的细胞形态在相对比图像中不会发生显着变化;图像特征不能为无标签图像的二维神经网络模型提供足够的判别。然而,这些细胞在分裂过程中没有明显的移动,并且它们表现出明显的时间形态模式。因此,我们可以及时地通过图像叠加来检测细胞分裂。通过结合3D神经网络应用于延时数据来寻找细胞分裂活动区域,然后在这些选定区域的图像中使用2D神经网络来寻找单个分裂细胞,我们开发了一个强大的iPS细胞分裂检测器。我们创建了一个初始的3D神经网络来查找(x,y,t)中识别细胞分裂发生的3D图像区域,然后使用带有额外图像堆栈的半监督训练来创建更精细的3D模型。然后用我们的二维神经网络推断这些区域,找到细胞分裂前的位置和时间,当它们包含两组染色质时,需要跟踪分裂后的细胞信息。通过添加2D模型,可以识别并去除3D推断结果中的假阳性。我们在手动标注的测试图像堆栈中成功识别了38个细胞分裂事件中的37个,并在分裂前以10像素的精度指定了每个细胞的时间和(x,y)位置。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Semi-supervised 3D neural networks to track iPS cell division in label-free phase contrast time series images
In order to predict cell population behavior, it is important to understand the dynamic characteristics of individual cells. Individual induced pluripotent stem (iPS) cells in colonies have been difficult to track over long times, both because segmentation is challenging due to close proximity of cells and because cell morphology at the time of cell division does not change dramatically in phase contrast images; image features do not provide sufficient discrimination for 2D neural network models of label-free images. However, these cells do not move significantly during division, and they display a distinct temporal pattern of morphologies. As a result, we can detect cell division with images overlaid in time. Using a combination of a 3D neural network applied over time-lapse data to find regions of cell division activity, followed by a 2D neural network for images in these selected regions to find individual dividing cells, we developed a robust detector of iPS cell division. We created an initial 3D neural network to find 3D image regions in (x,y,t) in which identified cell divisions occurred, then used semi-supervised training with additional stacks of images to create a more refined 3D model. These regions were then inferenced with our 2D neural network to find the location and time immediately before cells divide when they contain two sets of chromatin, information needed to track the cells after division. False positives from the 3D inferenced results were identified and removed with the addition of the 2D model. We successfully identified 37 of the 38 cell division events in our manually annotated test image stack, and specified the time and (x,y) location of each cell just before division within an accuracy of 10 pixels.
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