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Linear Discrimination, Ordination, and the Visualization of Selection Gradients in Modern Morphometrics

机译:线性判别,排序和现代形态计量学中选择梯度的可视化

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Linear discriminant analysis (LDA) is a multivariate classification technique frequently applied to morphometric data in various biomedical disciplines. Canonical variate analysis (CVA), the generalization of LDA for multiple groups, is often used in the exploratory style of an ordination technique (a low-dimensional representation of the data). In the rare case when all groups have the same covariance matrix, maximum likelihood classification can be based on these linear functions. Both LDA and CVA require full-rank covariance matrices, which is usually not the case in modern morphometrics. When the number of variables is close to the number of individuals, groups appear separated in a CVA plot even if they are samples from the same population. Hence, reliable classification and assessment of group separation require many more organisms than variables. A simple alternative to CVA is the projection of the data onto the principal components of the group averages (between-group PCA). In contrast to CVA, these axes are orthogonal and can be computed even when the data are not of full rank, such as for Procrustes shape coordinates arising in samples of any size, and when covariance matrices are heterogeneous. In evolutionary quantitative genetics, the selection gradient is identical to the coefficient vector of a linear discriminant function between the populations before vs. after selection. When the measured variables are Procrustes shape coordinates, discriminant functions and selection gradients are vectors in shape space and can be visualized as shape deformations. Except for applications in quantitative genetics and in classification, however, discriminant functions typically offer no interpretation as biological factors.
机译:线性判别分析(LDA)是一种多变量分类技术,经常应用于各种生物医学学科的形态计量数据。规范变量分析(CVA)是LDA对多个组的通用化,通常用于协调技术的探索式(数据的低维表示)。在极少数情况下,当所有组都具有相同的协方差矩阵时,最大似然分类可以基于这些线性函数。 LDA和CVA都需要完整的协方差矩阵,这在现代形态计量学中通常不是这种情况。当变量的数量接近个体的数量时,即使组是来自相同总体的样本,组也会在CVA图中显得分离。因此,可靠的分类和分类评估需要比变量更多的生物。 CVA的一个简单替代方法是将数据投影到组平均值(组PCA之间)的主要成分上。与CVA相反,这些轴是正交的,即使在数据不是完整等级时也可以计算出这些轴,例如,对于任何大小的样本中出现的Procrustes形状坐标,以及协方差矩阵都是异构的。在进化定量遗传学中,选择梯度与选择之前和之后的种群之间线性判别函数的系数向量相同。当测得的变量是Procrustes形状坐标时,判别函数和选择梯度是形状空间中的矢量,并且可以可视化为形状变形。但是,除了在定量遗传学和分类中的应用外,判别功能通常无法解释为生物学因素。

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