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A new normalization for Nanostring nCounter gene expression data

机译:纳米突发性基因表达数据的新标准化

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The Nanostring nCounter gene expression assay uses molecular barcodes and single molecule imaging to detect and count hundreds of unique transcripts in a single reaction. These counts need to be normalized to adjust for the amount of sample, variations in assay efficiency and other factors. Most users adopt the normalization approach described in the nSolver analysis software, which involves background correction based on the observed values of negative control probes, a within-sample normalization using the observed values of positive control probes and normalization across samples using reference (housekeeping) genes. Here we present a new normalization method, Removing Unwanted Variation-III (RUV-III), which makes vital use of technical replicates and suitable control genes. We also propose an approach using pseudo-replicates when technical replicates are not available. The effectiveness of RUV-III is illustrated on four different datasets. We also offer suggestions on the design and analysis of studies involving this technology.
机译:纳米管道NCounter基因表达测定法使用分子条形码和单分子成像来检测并计数单一反应中的数百种独特的转录物。这些计数需要归一化以调整样品量,测定效率和其他因素的变化。大多数用户采用NSOLVER分析软件中描述的归一化方法,该方法涉及基于所观察到的负控制探针的值的背景校正,使用参考(管家)基因在样品中观察到的阳性控制探针和标准化的样本范围内的样本标准化。 。在这里,我们提出了一种新的归一化方法,去除不需要的变异-III(RUV-III),这使得可以实现技术复制和合适的对照基因。当技术复制不可用时,我们还提出了一种使用伪复制的方法。 Ruv-III的有效性在四个不同的数据集中示出。我们还提供了关于涉及这项技术的研究的设计和分析的建议。

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