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Integration of DNA ligation and rolling circle amplification for the homogeneous, end-point detection of single nucleotide polymorphisms

机译:DNA连接和滚环扩增的整合,可用于单核苷酸多态性的均一,终点检测

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Association studies using common sequence variants or single nucleotide polymorphisms (SNPs) may provide a powerful approach to dissect the genetic inheritance of common complex traits. Such studies necessitate the development of cost-effective, high throughput technologies for scoring SNPs. The method described in this paper for the co-detection of both alleles of a SNP in a single homogeneous reaction combines the specificity of a high fidelity DNA ligation step with the power of rolling circle amplification. The incorporation of Amplifluor? energy transfer primers enables signal detection in a homogeneous format, making this approach highly amenable to automation. The adaptation of the genotyping method for high throughput screening using conventional liquid handling systems is described.
机译:使用常见序列变异或单核苷酸多态性(SNP)的关联研究可能提供一种强有力的方法来剖析常见复杂性状的遗传遗传。这些研究需要开发具有成本效益的高通量技术来对SNP进行评分。本文描述的用于在单个均相反应中共同检测SNP的两个等位基因的方法将高保真DNA连接步骤的特异性与滚环扩增的能力结合在一起。合并Amplifluor吗?能量转移引物可实现均质格式的信号检测,从而使此方法高度适合自动化。描述了基因分型方法用于使用常规液体处理系统进行高通量筛选的方法。

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