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A Comparison of Optimality Measures for Estimating Untyped SNP Using the Allele Frequencies of Neighboring SNPs

机译:使用邻近SNP的等位基因频率估计无类型SNP的最佳方法的比较

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摘要

The allele frequencies of Single Nucleotide Polymorphisms (SNPs) are important summary information in case-control Genome Wide Association Studies (GWASs) for computing test statistics and allelic odds ratios, which are used to identify significant SNPs or for meta-analysis. Due to the limitation of time and cost, a large fraction of the known SNPs are not genotyped in the current genotyping platforms used in most of the GWASs. Imputation methods of untyped SNPs based on the individual level of genotyped data are powerful tools. However, these methods are computationally expensive and cannot work in cases where only the summary level information, such as the allele frequency is available. In this study, we propose an approach of imputing the allele frequency of untyped SNPs in the sample using only the allele frequency of the most informative pair of SNPs. We apply and compare five information measures as multilocus information measures to determine the most informative pair of SNPs to impute the allele frequency of untyped SNPs. Our approach is simple, yet highly accurate in estimating the allele frequency of untyped SNPs.
机译:单核苷酸多态性(SNP)的等位基因频率是病例对照基因组广泛关联研究(GWAS)中重要的摘要信息,用于计算测试统计信息和等位基因比值比,这些比值用于识别重要的SNP或进行荟萃分析。由于时间和成本的限制,在大多数GWAS中使用的当前基因分型平台中,大部分已知SNP均未进行基因分型。基于基因型数据个体水平的无类型SNP的插补方法是强大的工具。但是,这些方法在计算上很昂贵,并且在只有摘要级别信息(例如等位基因频率)可用的情况下无法使用。在这项研究中,我们提出了一种仅使用信息最丰富的SNP对的等位基因频率来估算样品中未分型SNP的等位基因频率的方法。我们应用并比较了五个信息量度作为多位点信息量度,以确定最有信息量的SNP对,以估算未分型SNP的等位基因频率。我们的方法很简单,但是在估计未分型SNP的等位基因频率时非常准确。

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