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Combining allele-specific fluorescent probes and restriction assay in real-time PCR to achieve SNP scoring beyond allele ratios of 1:1000.

机译:将等位基因特异的荧光探针和限制性内切酶检测结合在实时PCR中,以实现等位基因比例超过1:1000的SNP得分。

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摘要

TaqMan-nuclease assays are widely used for the qualitative detection of single nucleotide polymorphisms (SNPs) and the determination of biallelic states in pooled or heterozygous DNA samples. These assays are highly specific, reproducible, and suitable for high-throughput approaches. A crucial limitation of this method, and others, is the detection qf minor allele frequencies with detection limits of generally 3% to 9% for minor allele contributions. Here we describe the combination of customized TaqMan-nuclease assay and allele-specific restriction to increase the sensitivity of this method, allowing the qualitative detection of allele contributions as low as 0.05%.
机译:TaqMan核酸酶测定法广泛用于定性检测单核苷酸多态性(SNP)和确定合并的或杂合的DNA样品中的双等位基因状态。这些测定具有高度特异性,可重复性,适用于高通量方法。该方法及其他方法的一个关键限制是检测qf次要等位基因频率,对于次要等位基因贡献,检测极限通常为3%到9%。在这里,我们描述了定制的TaqMan核酸酶测定法和等位基因特异性限制的结合,以提高该方法的敏感性,从而使等位基因贡献的定性检测低至0.05%。

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