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Automated Matching of Genomic Structures in Microscopic Images of Living Cells Using an Information Theoretic Approach

机译:使用信息论方法自动匹配活细胞显微图像中的基因组结构

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Advances in microscopic imaging technology have revolutionized biology in recent years by enabling the study of dynamic processes inside living cells. Time-lapse microscopy produces large numbers of sequential images of living cells taken over time. In this paper we describe the novel approaches we have developed to automate and introduce high accuracy to the process of identifying genomic structures in living cells and matching them between consecutive time-points. We derive control points from landmarks within the structures and use the Kulback-Leibler divergence as an information-theoretic approach to correctly resolve potential close matches within the iterative closest point (ICP) algorithm. We also describe the steps needed to extend our techniques to analyze three dimensional voxel images. The approaches we describe are widely applicable in the analysis of time-lapse microscopy data
机译:近年来,显微成像技术的进步使人们能够研究活细胞内部的动态过程,从而彻底改变了生物学。延时显微镜可产生大量随时间推移而采集的活细胞的连续图像。在本文中,我们描述了我们开发的新颖方法,该方法可以自动化并向识别活细胞中的基因组结构并将其在连续的时间点之间进行匹配的过程中引入了高精度。我们从结构中的地标派生控制点,并使用Kulback-Leibler散度作为信息理论方法来正确解决迭代最近点(ICP)算法中的潜在接近匹配。我们还描述了扩展我们的技术以分析三维体素图像所需的步骤。我们描述的方法可广泛应用于延时显微镜数据分析

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