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Perturbation analysis: a simple method for filtering SNPs with erroneous genotyping in genome-wide association studies.

机译:扰动分析:在全基因组关联研究中使用错误的基因分型过滤SNP的简单方法。

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摘要

We introduce a simple and yet scientifically objective criterion for identifying SNPs with genotyping errors due to poor clustering. This yields a metric for assessing the stability of the assigned genotypes by evaluating the extent of discordance between the calls made with the unperturbed and perturbed intensities. The efficacy of the metric is evaluated by: (1) estimating the extent of over-dispersion of the Hardy-Weinberg equilibrium chi-square test statistics; (2) an interim case-control study, where we investigated the efficacy of the introduced metric and standard quality control filters in reducing the number of SNPs with evidence of phenotypic association which are attributed to genotyping errors; (3) investigating the call and concordance rates of SNPs identified by perturbation analysis which have been genotyped on both Affymetrix and Illumina platforms. Removing SNPs identified by the extent of discordance can reduce the degree of over-dispersion of the HWE test statistic. Sensible use of perturbation analysis in an association study can correctly identify SNPs with problematic genotyping, reducing the number required for visual inspection. SNPs identified by perturbation analysis had lower call and concordance rates, and removal of these SNPs significantly improved the performance for the remaining SNPs.
机译:我们引入了一个简单而科学的客观标准来识别由于聚类不良而导致基因分型错误的SNP。这产生了一种度量,用于通过评估以未扰动强度和扰动强度进行的调用之间的不一致程度来评估分配的基因型的稳定性。该度量的有效性通过以下方式评估:(1)估计Hardy-Weinberg平衡卡方检验统计量的过度分散程度; (2)一项中期病例对照研究,我们调查了引入的度量标准和标准质量控制过滤器在减少SNP数量方面的功效,并减少了由于基因型错误导致的表型关联的证据; (3)研究通过扰动分析确定的SNP的调用率和一致性率,这些SNP在Affymetrix和Illumina平台上均已进行了基因分型。删除由不一致程度确定的SNP可以减少HWE测试统计数据的过度分散程度。在关联研究中合理使用扰动分析可以正确地识别出有问题的基因分型的SNP,从而减少了目视检查所需的数量。通过扰动分析确定的SNP具有较低的召集率和一致性率,并且删除这些SNP可以显着提高其余SNP的性能。

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