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Regression adjusted colocalisation colour mapping (RACC): A novel biological visual analysis method for qualitative colocalisation analysis of 3D fluorescence micrographs

机译:回归调整的分层化颜色映射(RACC):3D荧光显微照片定性分层分析的新型生物视觉分析方法

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The qualitative analysis of colocalisation in fluorescence microscopy is of critical importance to the understanding of biological processes and cellular function. However, the degree of accuracy achieved may differ substantially when executing different yet commonly utilized colocalisation analyses. We propose a novel biological visual analysis method that determines the correlation within the fluorescence intensities and subsequently uses this correlation to assign a colourmap value to each voxel in a three-dimensional sample while also highlighting volumes with greater combined fluorescence intensity. This addresses the ambiguity and variability which can be introduced into the visualisation of the spatial distribution of correlation between two fluorescence channels when the colocalisation between these channels is not considered. Most currently employed and generally accepted methods of visualising colocalisation using a colourmap can be negatively affected by this ambiguity, for example by incorrectly indicating non-colocalised voxels as positively correlated. In this paper we evaluate the proposed method by applying it to both synthetic data and biological fluorescence micrographs and demonstrate how it can enhance the visualisation in a robust way by visualising only truly colocalised regions using a colourmap to indicate the qualitative measure of the correlation between the fluorescence intensities. This approach may substantially support fluorescence microscopy applications in which precise colocalisation analysis is of particular relevance.
机译:荧光显微镜中的分层化定性分析对于对生物学过程和细胞功能的理解至关重要。然而,在执行不同且通常利用的离心化分析时,所达到的精度可能大大不同。我们提出了一种新的生物视觉分析方法,该方法确定荧光强度内的相关性,随后使用这种相关性,以将Colourmap值分配给三维样本中的每个体素,同时还突出显示具有更大组合荧光强度的体积。这解决了当不考虑这些通道之间的离心化时,可以将模糊性和可变性引入两个荧光通道之间的相关性之间的空间分布的可视化。最目前使用的和通常接受的使用Colourmap可视化Colocalisation的方法可以受到这种模糊性的负面影响,例如通过错误地表明非共聚的体素作为正相关。在本文中,我们通过将其应用于合成数据和生物荧光显微照片来评估所提出的方法,并通过使用Colourmap仅可视化真正的划分区域来表明它如何以稳健的方式增强可视化以指示所在的相关性荧光强度。该方法可以基本上支持荧光显微镜应用,其中精确的离子化分析特别相关。

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