首页> 美国卫生研究院文献>American Journal of Human Genetics >Rapid and Accurate Haplotype Phasing and Missing-Data Inference for Whole-Genome Association Studies By Use of Localized Haplotype Clustering
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Rapid and Accurate Haplotype Phasing and Missing-Data Inference for Whole-Genome Association Studies By Use of Localized Haplotype Clustering

机译:通过使用局部单倍型聚类进行全基因组关联研究的快速准确的单倍型定相和缺失数据推断

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摘要

Whole-genome association studies present many new statistical and computational challenges due to the large quantity of data obtained. One of these challenges is haplotype inference; methods for haplotype inference designed for small data sets from candidate-gene studies do not scale well to the large number of individuals genotyped in whole-genome association studies. We present a new method and software for inference of haplotype phase and missing data that can accurately phase data from whole-genome association studies, and we present the first comparison of haplotype-inference methods for real and simulated data sets with thousands of genotyped individuals. We find that our method outperforms existing methods in terms of both speed and accuracy for large data sets with thousands of individuals and densely spaced genetic markers, and we use our method to phase a real data set of 3,002 individuals genotyped for 490,032 markers in 3.1 days of computing time, with 99% of masked alleles imputed correctly. Our method is implemented in the Beagle software package, which is freely available.
机译:由于获得的大量数据,全基因组关联研究提出了许多新的统计和计算挑战。这些挑战之一是单倍型推断。为来自候选基因研究的少量数据而设计的单倍型推论方法不能很好地适应全基因组关联研究中大量基因分型的个体。我们提供了一种新的方法和软件来推断单倍型阶段和丢失的数据,可以准确地对来自全基因组关联研究的数据进行分相,并且我们针对具有数千个基因型个体的真实和模拟数据集,首次提出了单倍型推断方法的比较。我们发现,对于具有数千个个体和密集遗传标记的大型数据集,我们的方法在速度和准确性方面都优于现有方法,并且使用我们的方法在3.1天内分阶段了3,002个个体的真实数据集,这些个体被基因型划分为490,032个标记的计算时间,正确估算了99%的屏蔽等位基因。我们的方法在Beagle软件包中实现,该软件包可免费获得。

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