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Genetic Geostatistical Framework for Spatial Analysis of Fine-Scale Genetic Heterogeneity in Modern Populations: Results from the KORA Study

机译:现代人口中精细尺度遗传异质性空间分析的遗传地统计框架:KORA研究的结果

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摘要

Aiming to investigate fine-scale patterns of genetic heterogeneity in modern humans from a geographic perspective, a genetic geostatistical approach framed within a geographic information system is presented. A sample collected for prospective studies in a small area of southern Germany was analyzed. None indication of genetic heterogeneity was detected in previous analysis. Socio-demographic and genotypic data of German citizens were analyzed (212 SNPs; n = 728). Genetic heterogeneity was evaluated with observed heterozygosity (H O). Best-fitting spatial autoregressive models were identified, using socio-demographic variables as covariates. Spatial analysis included surface interpolation and geostatistics of observed and predicted patterns. Prediction accuracy was quantified. Spatial autocorrelation was detected for both socio-demographic and genetic variables. Augsburg City and eastern suburban areas showed higher H O values. The selected model gave best predictions in suburban areas. Fine-scale patterns of genetic heterogeneity were observed. In accordance to literature, more urbanized areas showed higher levels of admixture. This approach showed efficacy for detecting and analyzing subtle patterns of genetic heterogeneity within small areas. It is scalable in number of loci, even up to whole-genome analysis. It may be suggested that this approach may be applicable to investigate the underlying genetic history that is, at least partially, embedded in geographic data.
机译:为了从地理角度研究现代人类遗传异质性的精细模式,提出了一种在地理信息系统内构建的遗传地统计学方法。分析了在德国南部一小区域收集的用于前瞻性研究的样本。在先前的分析中未检测到遗传异质性的迹象。分析了德国公民的社会人口统计学和基因型数据(212个SNP; n = 728)。用观察到的杂合性(HO)评估遗传异质性。使用社会人口统计学变量作为协变量,确定了最合适的空间自回归模型。空间分析包括表面插值以及观测和预测模式的地统计学。预测准确性被量化。社会人口统计和遗传变量均检测到空间自相关。奥格斯堡市和东部郊区显示出较高的H O值。选择的模型在郊区提供了最佳预测。观察到遗传异质性的精细模式。根据文献,更多的城市化地区显示出更高水平的掺混物。这种方法显示出检测和分析小区域内遗传异质性细微模式的功效。它可以扩展基因座的数量,甚至可以扩展到全基因组分析。可能有人建议,这种方法可能适用于研究至少部分地嵌入地理数据中的潜在遗传历史。

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