活细胞成像中出发地交通估计的最小路径和概率模型

T. Pécot, C. Kervrann, P. Bouthemy
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引用次数: 9

摘要

绿色荧光蛋白(GFP)标记和延时荧光显微镜能够观察活细胞中的分子动力学和相互作用。然后需要原始图像分析方法来处理具有挑战性的2D或3D图像序列。为了解决数百个目标的跟踪问题,我们提出了一个原始框架,该框架提供了关于囊泡运输的一般信息,即图像序列中检测到的原点和目的地区域之间的交通流。流量估计可以通过采用网络通信中常用的网络层析成像技术来实现。在本文中,我们解决了给定囊泡储存区域的图像分割和囊泡运输的多路径路由问题。该方法已开发用于真实荧光图像序列和Rab蛋白。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Minimal paths and probabilistic models for origin-destination traffic estimation in live cell imaging
Green Fluorescent Protein (GFP)-tagging and time-lapse fluorescence microscopy enable to observe molecular dynamics and interactions in live cells. Original image analysis methods are then required to process challenging 2D or 3D image sequences. To address the tracking problem of several hundreds of objects, we propose an original framework that provides general information about vesicle transport, that is traffic flows between origin and destination regions detected in the image sequence. Traffic estimation can be accomplished by adapting the advances in Network Tomography commonly used in network communications. In this paper, we address image partition given vesicle stocking areas and multipaths routing for vesicle transport. This approach has been developed for real fluorescence image sequences and Rab proteins.
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