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Closed-form density-based framework for automatic detection of cellular morphology changes

机译:基于封闭形式的密度的框架,用于自动检测细胞形态变化

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A primary method for studying cellular function is to examine cell morphology after a given manipulation. Fluorescent markers attached to proteins/intracellular structures of interest in conjunction with 3D fluorescent microscopy are frequently exploited for functional analysis. Despite the central role of morphology comparisons in cell biological approaches, few statistical tools are available that allow biological scientists without a high level of statistical training to quantify the similarity or difference of fluorescent images containing multifactorial information. We transform intracellular structures into kernels and develop a multivariate two-sample test that is nonparametric and asymptotically normal to directly and quantitatively compare cellular morphologies. The asymptotic normality bypasses the computationally intensive calculations used by the usual resampling techniques to compute the P-value. Because all parameters required for the statistical test are estimated directly from the data, it does not require any subjective decisions. Thus, we provide a black-box method for unbiased, automated comparison of cell morphology. We validate the performance of our test statistic for finite synthetic samples and experimental data. Employing our test for the comparison of the morphology of intracellular multivesicular bodies, we detect changes in their distribution after disruption of the cellular microtubule cytoskeleton with high statistical significance in fixed samples and live cell analysis. These results demonstrate that density-based comparison of multivariate image information is a powerful tool for automated detection of cell morphology changes. Moreover, the underlying mathematics of our test statistic is a general technique, which can be applied in situations where two data samples are compared.
机译:研究细胞功能的主要方法是检查给定操作后的细胞形态。结合3D荧光显微镜将感兴趣的蛋白质/细胞内结构上附着的荧光标记物经常用于功能分析。尽管形态学比较在细胞生物学方法中起着核心作用,但很少有统计工具可用于使生物学家无需经过高水平的统计培训即可量化包含多因素信息的荧光图像的相似性或差异性。我们将细胞内结构转化为内核,并开发了多参数两样本检验,该检验非参数且渐近正常,可以直接和定量比较细胞形态。渐近正态性绕过了通常的重采样技术用来计算P值的计算量大的计算。由于统计测试所需的所有参数都是直接从数据中估算的,因此不需要任何主观决定。因此,我们为细胞形态的无偏自动比较提供了一种黑盒方法。我们针对有限的合成样本和实验数据验证了测试统计量的性能。使用我们的测试来比较细胞内多囊泡体的形态,我们检测到在固定样品和活细胞分析中具有高统计意义的细胞微管细胞骨架破裂后它们分布的变化。这些结果表明,基于密度的多元图像信息比较是用于自动检测细胞形态变化的强大工具。此外,我们的测试统计量的基础数学是一种通用技术,可用于比较两个数据样本的情况。

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