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High-Performance Multiplex SNP Analysis of Three Hemochromatosis-Related Mutations With Capillary Array Electrophoresis Microplates

机译:用毛细管阵列电泳微孔板对三种血色素沉着相关突变的高效能多重单核苷酸多态性分析

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摘要

An assay is described for high-throughput single nucleotide polymorphism (SNP) genotyping on a microfabricated capillary array electrophoresis (CAE) microchip. The assay targets the three common variants at the HFE locus associated with the genetic disease hereditary hemochromatosis (HHC). The assay employs allele-specific PCR (ASPCR) for the C282Y (845g->a), H63D (187c->g), and S65C (193a->t) variants using fluorescently-labeled energy-transfer (ET) allele-specific primers. Using a 96-channel radial CAE microplate, the labeled ASPCR products generated from 96 samples in a reference Caucasian population are simultaneously separated with single-base-pair resolution and genotyped in under 10 min. Detection is accomplished with a laser-excited rotary four-color fluorescence scanner. The allele-specific amplicons are differentiated on the basis of both their size and the color of the label emission. This study is the first demonstration of the combined use of ASPCR with ET primers and microfabricated radial CAE microplates to perform multiplex SNP analyses in a clinically relevant population.
机译:描述了一种在微细毛细管阵列电泳(CAE)微芯片上进行高通量单核苷酸多态性(SNP)基因分型的测定方法。该测定法针对与遗传疾病遗传性血色素沉着病(HHC)相关的HFE基因座的三个常见变异。该方法使用荧光标记的能量转移(ET)等位基因特异的C282Y(845g-> a),H63D(187c-> g)和S65C(193a-> t)变体采用等位基因特异性PCR(ASPCR)底漆。使用96通道放射状CAE微孔板,以单碱基对分辨率同时分离从参考白种人人群中的96个样品产生的标记ASPCR产物,并在10分钟内进行基因分型。用激光激发的旋转四色荧光扫描仪完成检测。等位基因特异性扩增子基于其大小和标记发射的颜色进行区分。这项研究是ASPCR与ET引物和微型放射状CAE微孔板结合使用以在临床相关人群中进行多重SNP分析的第一个证明。

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