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Feasibility of High-Throughput Genome-Wide Genotyping using DNA from Stored Buccal Cell Samples

机译:使用来自存储的颊细胞样品中的DNA进行高通量基因组全基因型分型的可行性

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摘要

It is unclear if buccal cell samples contain sufficient human DNA with adequately sized fragments for high throughput genetic bioassays. Yet buccal cell sample collection is an attractive alternative to gathering blood samples for genetic epidemiologists engaged in large-scale genetic biomarker studies. We assessed the genotyping efficiency (GE) and genotyping concordance (GC) of buccal cell DNA samples compared to corresponding blood DNA samples, from 32 Nurses’ Health Study (NHS) participants using the Illumina Infinium 660W-Quad platform. We also assessed how GE and GC accuracy varied as a function of DNA concentration using serial dilutions of buccal DNA samples. Finally we determined the nature and genomic distribution of discordant genotypes in buccal DNA samples. The mean GE of undiluted buccal cell DNA samples was high (99.32%), as was the GC between the paired buccal and blood samples (99.29%). GC between the dilutions versus the undiluted buccal DNA was also very high (>97%), though both GE and GC notably declined at DNA concentrations less than 5 ng/μl. Most (>95%) genotype determinations in buccal cell samples were of the “missing call” variety (as opposed to the “alternative genotype call” variety) across the spectrum of buccal DNA concentrations studied. Finally, for buccal DNA concentration above 1.7 ng/ul, discordant genotyping calls did not cluster in any particular chromosome. Buccal cell-derived DNA represents a viable alternative to blood DNA for genotyping on a high-density platform.
机译:目前尚不清楚颊细胞样品是否包含足够的人类DNA和足够大小的片段,可用于高通量遗传生物测定。然而,对于从事大规模遗传生物标记研究的遗传流行病学家来说,颊细胞样本采集是一种替代血液采集的有吸引力的选择。我们使用Illumina Infinium 660W-Quad平台评估了来自32名护士健康研究(NHS)参与者的颊细胞DNA样品与相应血液DNA样品的基因分型效率(GE)和基因分型一致性(GC)。我们还使用口腔DNA样品的连续稀释液评估了GE和GC的准确度如何随DNA浓度的变化而变化。最后,我们确定颊DNA样本中不一致基因型的性质和基因组分布。未稀释的颊细胞DNA样品的平均GE值很高(99.32%),配对的颊和血液样品之间的GC值也很高(99.29%)。稀释液与未稀释颊DNA之间的GC值也很高(> 97%),尽管当DNA浓度低于5 ng /μl时,GE和GC均显着下降。颊细胞样本中大多数(> 95%)基因型测定是在所研究的颊DNA浓度范围内属于“遗漏”变种(与“替代基因型称为”变种相反)。最后,对于高于1.7 ng / ul的颊含DNA浓度,不一致的基因分型方法没有聚集在任何特定的染色体中。颊细胞衍生的DNA代表了在高密度平台上进行基因分型的血液DNA的可行选择。

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