首页> 外文期刊>RNA >Systematic evaluation of medium-throughput mRNA abundance platforms
【24h】

Systematic evaluation of medium-throughput mRNA abundance platforms

机译:中通量mRNA丰度平台的系统评估

获取原文
获取原文并翻译 | 示例
           

摘要

Profiling of mRNA abundances with high-throughput platforms such as microarrays and RNA-seq has become an important tool in both basic and biomedical research. However, these platforms remain prone to systematic errors and have challenges in clinical and industrial applications. As a result, it is standard practice to validate a subset of key results using alternate technologies. Similarly, clinical and industrial applications typically involve transitions from a high-throughput discovery platform to medium-throughput validation ones. These medium-throughput validation platforms have high technical reproducibility and reduced sample input needs, and low sensitivity to sample quality (e.g., for processing FFPE specimens). Unfortunately, while medium-throughput platforms have proliferated, there are no comprehensive comparisons of them. Here we fill that gap by comparing two key medium-throughput platforms - NanoString's nCounter Analysis System and ABI's OpenArray System - to gold-standard quantitative real-time RT-PCR. We quantified 38 genes and positive and negative controls in 165 samples. Signal:noise ratios, correlations, dynamic range, and detection accuracy were compared across platforms. All three measurement technologies showed good concordance, but with divergent price/time/sensitivity trade-offs. This study provides the first detailed comparison of medium-throughput RNA quantification platforms and provides a template and a standard data set for the evaluation of additional technologies.
机译:使用高通量平台(例如微阵列和RNA-seq)分析mRNA丰度已成为基础研究和生物医学研究的重要工具。但是,这些平台仍然容易出现系统错误,并且在临床和工业应用中都面临挑战。因此,使用替代技术来验证关键结果的子集是标准做法。同样,临床和工业应用通常涉及从高通量发现平台到中通量验证平台的过渡。这些中等通量验证平台具有很高的技术可重复性和减少的样品输入需求,并且对样品质量的敏感性较低(例如,用于处理FFPE样品)。不幸的是,尽管中吞吐量平台激增了,但还没有对其进行全面的比较。在这里,我们通过比较两个关键的中通量平台(NanoString的nCounter分析系统和ABI的OpenArray系统)与金标准的定量实时RT-PCR来填补这一空白。我们对165个样品中的38个基因以及阳性和阴性对照进行了定量。比较了跨平台的信噪比,相关性,动态范围和检测精度。三种测量技术都显示出良好的一致性,但是在价格/时间/灵敏度方面存在不同的取舍。这项研究提供了中通量RNA定量平台的首次详细比较,并提供了用于评估其他技术的模板和标准数据集。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

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