首页> 外文期刊>Clinical Chemistry: Journal of the American Association for Clinical Chemists >Analytical Validation of the Tag-It High-Throughput Microsphere-Based Universal Array Genotyping Platform: Application to the Multiplex Detection of a Panel of Thrombophilia-Associated Single-Nucleotide Polymorphisms
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Analytical Validation of the Tag-It High-Throughput Microsphere-Based Universal Array Genotyping Platform: Application to the Multiplex Detection of a Panel of Thrombophilia-Associated Single-Nucleotide Polymorphisms

机译:Tag-It高通量微球为基础的通用阵列基因分型平台的分析验证:应用于血友病相关的单核苷酸多态性面板的多重检测。

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Background: We have developed a novel, microsphere-based universal array platform referred to as the Tag-It? platform. This platform is suitable for high-throughput clinical genotyping applications and was used for multiplex analysis of a panel of thrombophilia-associated single-nucleotide polymorphisms (SNPs).Methods: Genomic DNA from 132 patients was amplified by multiplex PCR using 6 primer sets, followed by multiplex allele-specific primer extension using 12 universally tagged genotyping primers. The products were then sorted on the Tag-It array and detected by use of the Luminex xMAP? system. Genotypes were also determined by sequencing.Results: Empirical validation of the universal array showed that the highest nonspecific signal was 3.7% of the specific signal. Patient genotypes showed 100% concordance with direct DNA sequencing data for 736 SNP determinations.Conclusions: The Tag-It microsphere-based universal array platform is a highly accurate, multiplexed, high-throughput SNP-detection platform.
机译:背景:我们已经开发了一种新颖的基于微球的通用阵列平台,称为Tag-It?平台。该平台适用于高通量临床基因分型应用,并用于一组与血友病相关的单核苷酸多态性(SNP)的多重分析。方法:采用6个引物组,通过多重PCR扩增了132例患者的基因组DNA。通过使用12种普遍标记的基因分型引物对等位基因特异性引物进行多重延伸。然后将产品在Tag-It阵列上分类,并使用Luminex xMAP?进行检测。系统。结果:通用阵列的经验验证表明,最高的非特异性信号是特异性信号的3.7%。患者基因型与736个SNP测定的直接DNA测序数据显示出100%的一致性。结论:基于Tag-It微球的通用阵列平台是一种高精度,多重,高通量SNP检测平台。

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