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Development of an automated SNP analysis method using a paramagnetic beads handling robot

机译:使用顺磁珠处理机器人开发自动SNP分析方法

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Biological and medical importance of the single nucleotide polymorphism (SNP) has led to development of a wide variety of methods for SNP typing. Aiming for establishing highly reliable and fully automated SNP typing, I we have developed the adapter ligation method in combination with the paramagnetic beads handling technology, Magtrationo((R)). The method utilizes sequence specific ligation between the fluorescently labeled adapter and the sample DNAs at the cohesive end produced by a type IIS restriction enzyme. Evaluation of the method using human genomic DNA showed clear discrimination of the three genotypes without ambiguity using the same reaction condition for any SNPs examined. The operations following PCR amplification were automatically performed by the Magtration based robot that we have previously developed. Multiplex typing of two SNPs in a, single reaction by using four fluorescent dyes was successfully preformed at the almost same sensitivity and reliability as the single typing. These results demonstrate that the automated paramagnetic beads handling technology, Magtration((R)), is highly adaptable to the automated SNP analysis and that our method best fits to an automated in-house SNP typing for laboratory and medical uses.
机译:单核苷酸多态性(SNP)的生物学和医学重要性导致了各种各样的SNP分型方法的发展。为了建立高度可靠且全自动的SNP分型,我们开发了结合顺磁性珠粒处理技术Magtrationo(R)的衔接子连接方法。该方法利用了荧光标记的衔接子与由IIS型限制酶产生的内聚末端的样品DNA之间的序列特异性连接。使用人类基因组DNA对该方法进行的评估表明,对于所检查的任何SNP,使用相同的反应条件,可以清楚地区分三种基因型。 PCR扩增后的操作由我们先前开发的基于Magtration的机器人自动执行。通过使用四种荧光染料在单个反应中成功完成了两个SNP的多重分型,其灵敏度和可靠性几乎与单一分型相同。这些结果表明,自动顺磁珠处理技术Magtration(R)非常适合自动SNP分析,并且我们的方法最适合实验室和医学用途的自动内部SNP分型。

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