A High-throughput Real-time PCR Approach to Pharmacogenomics Studies

T. Hartshorne, F. Le, Jordan Lang, H. Leong, K. Hayashibara, D. Dewolf, Elliot J Shelton
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引用次数: 10

Abstract

Advances in personalized medicine have led to an increase in pharmacogenomics studies that involve testing individuals for drug metabolism enzyme and transporter gene polymorphisms implicated in drug response. As a consequence, there is a growing demand for affordable, easy to use technologies with fast sample-to-results workflows that can accommodate testing customizable sets of target gene variants and a changeable number of samples. Additionally, data analysis tools are needed to facilitate translation of an individual’s genetic information to their diploid content of gene-level star allele haplotypes, which can be correlated with drug metabolism enzyme phenotypes. Here we describe the development of a comprehensive pharmacogenomics experiments workflow solution to meet this need. High quality data was generated from purified buccal swab DNAs run with TaqMan® SNP genotyping and copy number assays in OpenArray® and 384-well plate formats, respectively, on the QuantStudio™ 12K Flex system. Data analysis was accomplished using TaqMan® Genotyper™ Software to examine SNP genotyping assay results and CopyCaller® Software to examine copy number assay results, followed by translation of this genetic data for individual samples to star allele genotypes using the recently developed AlleleTyper™ Software. The specific TaqMan® SNP Genotyping and Copy Number Assays to gene variants used can be tailored to suit the needs of a given pharmacogenomics study. This low cost, high throughput pharmacogenomics workflow can be completed in a single day, from sample preparation to data analysis.
药物基因组学研究的高通量实时PCR方法
个性化医疗的进步导致了药物基因组学研究的增加,这些研究涉及检测与药物反应有关的药物代谢酶和转运基因多态性。因此,对价格合理、易于使用的技术的需求不断增长,这些技术具有快速的样品到结果工作流程,可以适应测试可定制的目标基因变体集和可变数量的样品。此外,还需要数据分析工具来将个体的遗传信息翻译成与药物代谢酶表型相关的基因水平星型等位基因单倍型的二倍体含量。在这里,我们描述了一个全面的药物基因组学实验工作流程解决方案的发展,以满足这一需求。纯化的口腔拭子dna在QuantStudio™12K Flex系统上分别以OpenArray®和384孔板格式进行TaqMan®SNP基因分型和拷贝数分析,产生高质量的数据。使用TaqMan®Genotyper™软件检查SNP基因分型分析结果和CopyCaller®软件检查拷贝数分析结果完成数据分析,然后使用最近开发的AlleleTyper™软件将单个样品的遗传数据翻译为等位基因型。特定的TaqMan®SNP基因分型和拷贝数测定可用于基因变异,以适应特定药物基因组学研究的需要。这种低成本、高通量的药物基因组学工作流程可以在一天内完成,从样品制备到数据分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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