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Detection of genotyping errors by Hardy-Weinberg equilibrium testing.

机译:通过Hardy-Weinberg平衡测试检测基因分型错误。

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摘要

Genotyping data sets may contain errors that, in some instances, lead to false conclusions. Deviation from Hardy-Weinberg equilibrium (HWE) in random samples may be indicative of problematic assays. This study has analysed 107,000 genotypes generated by TaqMan, RFLP, sequencing or mass spectrometric methods from 443 single-nucleotide polymorphisms (SNPs). These SNPs are distributed both within genes and in intergenic regions. Genotype distributions for 36 out of 313 assays (11.5%) whose minor allele frequencies were >0.05 deviated from HWE (P<0.05). Some of the possible reasons for this deviation were explored: assays for five SNPs proved nonspecific, and genotyping errors were identified in 21 SNPs. For the remaining 10 SNPs, no reasons for deviation from HWE were identified. We demonstrate the successful identification of a proportion of nonspecific assays, and assays harbouring genotyping error. Consequently, our current high-throughput genotyping system incorporates tests for both assay specificityand deviation from HWE, to minimise the genotype error rate and therefore improve data quality.
机译:基因分型数据集可能包含错误,在某些情况下会导致错误的结论。随机样品中哈迪-温伯格平衡(HWE)的偏离可能表明测定存在问题。这项研究分析了TaqMan,RFLP,测序或质谱法从443个单核苷酸多态性(SNP)产生的107,000个基因型。这些SNP既分布在基因内,又分布在基因间区域。 313个分析中的36个(11.5%)的基因型分布与HWE相比,其次要等位基因频率> 0.05(P <0.05)。探索了造成这种偏离的一些可能原因:对5个SNP的测定证明是非特异性的,并且在21个SNP中鉴定出基因分型错误。对于其余的10个SNP,没有发现偏离HWE的原因。我们证明了一部分非特异性测定的成功鉴定,以及具有基因分型错误的测定。因此,我们当前的高通量基因分型系统结合了针对检测特异性和与HWE的偏差的测试,以最大程度地减少基因型错误率,从而提高数据质量。

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