首页> 美国卫生研究院文献>PLoS Clinical Trials >Melt Analysis of Mismatch Amplification Mutation Assays (Melt-MAMA): A Functional Study of a Cost-Effective SNP Genotyping Assay in Bacterial Models
【2h】

Melt Analysis of Mismatch Amplification Mutation Assays (Melt-MAMA): A Functional Study of a Cost-Effective SNP Genotyping Assay in Bacterial Models

机译:失配扩增突变分析(Melt-MAMA)的熔体分析:在细菌模型中进行具有成本效益的SNP基因分型分析的功能研究

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Single nucleotide polymorphisms (SNPs) are abundant in genomes of all species and biologically informative markers extensively used across broad scientific disciplines. Newly identified SNP markers are publicly available at an ever-increasing rate due to advancements in sequencing technologies. Efficient, cost-effective SNP genotyping methods to screen sample populations are in great demand in well-equipped laboratories, but also in developing world situations. Dual Probe TaqMan assays are robust but can be cost-prohibitive and require specialized equipment. The Mismatch Amplification Mutation Assay, coupled with melt analysis (Melt-MAMA), is flexible, efficient and cost-effective. However, Melt-MAMA traditionally suffers from high rates of assay design failures and knowledge gaps on assay robustness and sensitivity. In this study, we identified strategies that improved the success of Melt-MAMA. We examined the performance of 185 Melt-MAMAs across eight different pathogens using various optimization parameters. We evaluated the effects of genome size and %GC content on assay development. When used collectively, specific strategies markedly improved the rate of successful assays at the first design attempt from ∼50% to ∼80%. We observed that Melt-MAMA accurately genotypes across a broad DNA range (∼100 ng to ∼0.1 pg). Genomic size and %GC content influence the rate of successful assay design in an independent manner. Finally, we demonstrated the versatility of these assays by the creation of a duplex Melt-MAMA real-time PCR (two SNPs) and conversion to a size-based genotyping system, which uses agarose gel electrophoresis. Melt-MAMA is comparable to Dual Probe TaqMan assays in terms of design success rate and accuracy. Although sensitivity is less robust than Dual Probe TaqMan assays, Melt-MAMA is superior in terms of cost-effectiveness, speed of development and versatility. We detail the parameters most important for the successful application of Melt-MAMA, which should prove useful to the wider scientific community.
机译:单核苷酸多态性(SNP)在所有物种的基因组中都很丰富,并且在广泛的科学学科中广泛使用的生物学信息标记。由于测序技术的进步,新近鉴定出的SNP标记以越来越高的速度公开获得。在装备精良的实验室中以及在发展中国家的情况下,对筛选样品种群的高效,具成本效益的SNP基因分型方法的需求很大。 Dual Probe TaqMan测定法功能强大,但成本高昂,需要专门的设备。错配扩增突变分析与熔体分析(Melt-MAMA)相结合,具有灵活性,效率和成本效益。然而,传统上,Melt-MAMA存在检定设计失败率高以及检定鲁棒性和灵敏度方面的知识空白的问题。在这项研究中,我们确定了改善Melt-MAMA成功的策略。我们使用各种优化参数检查了185种Melt-MAMA在8种不同病原体上的性能。我们评估了基因组大小和%GC含量对测定开发的影响。当共同使用时,特定的策略可将首次设计尝试中成功测定的比率从〜50%显着提高到〜80%。我们观察到,Melt-MAMA在广泛的DNA范围(约100 ng至约0.1 pg)中准确地确定了基因型。基因组大小和%GC含量以独立的方式影响成功的测定设计的速度。最后,我们通过创建双重Melt-MAMA实时PCR(两个SNP)并转换为基于大小的基因分型系统(使用琼脂糖凝胶电泳)证明了这些测定方法的多功能性。在设计成功率和准确性方面,Melt-MAMA可与Dual Probe TaqMan分析相媲美。尽管灵敏度不如Dual Probe TaqMan测定法强,但Melt-MAMA在成本效益,开发速度和多功能性方面均优越。我们详细介绍了成功应用Melt-MAMA最重要的参数,这些参数应被证明对更广泛的科学界有用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号