首页> 外文期刊>Theoretical and Applied Genetics: International Journal of Breeding Research and Cell Genetics >Non-parametric smoothing of multivariate genetic distances in the analysis of spatial population structure at fine scale.
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Non-parametric smoothing of multivariate genetic distances in the analysis of spatial population structure at fine scale.

机译:精细尺度上空间种群结构分析中多元遗传距离的非参数平滑。

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Species dispersal studies provide valuable information in biological research. Restricted dispersal may give rise to a non-random distribution of genotypes in space. Detection of spatial genetic structure may therefore provide valuable insight into dispersal. Spatial structure has been treated via autocorrelation analysis with several univariate statistics for which results could dependent on sampling designs. New geostatistical approaches (variogram-based analysis) have been proposed to overcome this problem. However, modelling parametric variograms could be difficult in practice. We introduce a non-parametric variogram-based method for autocorrelation analysis between DNA samples that have been genotyped by means of multilocus-multiallele molecular markers. The method addresses two important aspects of fine-scale spatial genetic analyses: the identification of a non-random distribution of genotypes in space, and the estimation of the magnitude of any non-random structure. The method uses a plot of the squared Euclidean genetic distances vs. spatial distances between pairs of DNA-samples as empirical variogram. The underlying spatial trend in the plot is fitted by a non-parametric smoothing (LOESS, Local Regression). Finally, the predicted LOESS values are explained by segmented regressions (SR) to obtain classical spatial values such as the extent of autocorrelation. For illustration we use multivariate and single-locus genetic distances calculated from a microsatellite data set for which autocorrelation was previously reported. The LOESS/SR method produced a good fit providing similar value of published autocorrelation for this data. The fit by LOESS/SR was simpler to obtain than the parametric analysis since initial parameter values are not required during the trend estimation process. The LOESS/SR method offers a new alternative for spatial analysis.
机译:物种传播研究为生物学研究提供了有价值的信息。限制的传播可能会导致基因型在空间中的非随机分布。因此,空间遗传结构的检测可能会为传播提供有价值的见解。空间结构已通过自相关分析和几个单变量统计进行了处理,其结果可能取决于抽样设计。已经提出了新的地统计方法(基于变异函数的分析)来克服这个问题。但是,在实践中很难对参数变异函数建模。我们介绍了一种基于非参数变异函数的方法,用于通过多基因座-多等位基因分子标记进行基因分型的DNA样本之间的自相关分析。该方法解决了精细尺度空间遗传分析的两个重要方面:识别空间中基因型的非随机分布,以及估计任何非随机结构的大小。该方法使用欧几里德遗传距离平方对DNA样本对之间的空间距离作图作为经验变异函数。图中潜在的空间趋势通过非参数平滑法拟合(LOESS,局部回归)。最后,通过分段回归(SR)解释了预测的LOESS值,以获得经典的空间值,例如自相关程度。为了说明,我们使用从微卫星数据集计算得到的多变量和单基因座遗传距离,先前已针对该数据集进行了自相关。 LOESS / SR方法产生了很好的拟合度,为该数据提供了相似的已发布自相关值。 LOESS / SR的拟合比参数分析更容易获得,因为在趋势估计过程中不需要初始参数值。 LOESS / SR方法为空间分析提供了新的选择。

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