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首页> 外文期刊>Cytometry, Part A: the journal of the International Society for Analytical Cytology >Deformation-based nuclear morphometry: Capturing nuclear shape variation in HeLa cells
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Deformation-based nuclear morphometry: Capturing nuclear shape variation in HeLa cells

机译:基于变形的核形态:捕获HeLa细胞的核形状变化

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The empirical characterization of nuclear shape distributions is an important unsolved problem with many applications in biology and medicine. Numerous genetic diseases and cancers have alterations in nuclear morphology, and methods for characterization of morphology could aid in both diagnoses and fundamental understanding of these disorders. Automated approaches have been used to measure features related to the size and shape of the cell nucleus, and statistical analysis of these features has often been performed assuming an underlying Euclidean (linear) vector space. We discuss the difficulties associated with the analysis of nuclear shape in light of the fact that shape spaces are nonlinear, and demonstrate methods for characterizing nuclear shapes and shape distributions based on spatial transformations that map one nucleus to another. By combining large deformation metric mapping with multidimensional scaling we offer a flexible approach for elucidating the intrinsic nonlinear degrees of freedom of a distribution of nuclear shapes. More specifically, we demonstrate approaches for nuclear shape interpolation and computation of mean nuclear shape. We also provide a method for estimating the number of free parameters that contribute to shape as well as an approach for visualizing most representative shape variations within a distribution of nuclei. The proposed methodology can be completely automated, is independent of the dimensionality of the images, and can handle complex shapes. Results obtained by analyzing two sets of images of HeLa cells are shown. In addition to identifying the modes of variation in normal HeLa nuclei, the effects of lamin A/C on nuclear morphology are quantitatively described.
机译:核形状分布的经验表征是生物学和医学中许多应用中尚未解决的重要问题。许多遗传疾病和癌症的核形态都有变化,形态表征的方法可以帮助诊断和基本了解这些疾病。自动化方法已用于测量与细胞核的大小和形状有关的特征,并且通常在假设潜在的欧几里得(线性)向量空间的情况下对这些特征进行统计分析。鉴于形状空间是非线性的,我们讨论了与核形状分析相关的困难,并演示了基于将一个核映射到另一个核的空间变换来表征核形状和形状分布的方法。通过将大变形量度映射与多维缩放相结合,我们提供了一种灵活的方法来阐明核形状分布的固有非线性自由度。更具体地说,我们展示了用于核形状插值和平均核形状计算的方法。我们还提供了一种估计有助于形状的自由参数的数量的方法,以及一种可视化核分布内最具代表性的形状变化的方法。所提出的方法可以是完全自动化的,与图像的尺寸无关,并且可以处理复杂的形状。显示了通过分析两组HeLa细胞图像获得的结果。除了确定正常HeLa核的变异模式外,还定量描述了层粘蛋白A / C对核形态的影响。

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