Translational Genomics and Epigenomics Laboratory, Olivia Newton-John Cancer Research Institute, Heidelberg, Victoria 3084, Australia.
Bioinformatics Division, Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria 3052, Australia.
Nucleic Acids Res. 2019 Jul 9;47(12):6073-6083. doi: 10.1093/nar/gkz433.
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.
Nanostring nCounter 基因表达检测使用分子条码和单分子成像技术,在单个反应中检测和计数数百个独特的转录本。这些计数需要进行标准化,以调整样品量、检测效率等因素的影响。大多数用户采用 nSolver 分析软件中描述的标准化方法,该方法包括基于阴性对照探针观察值的背景校正、使用阳性对照探针观察值进行样本内标准化以及使用参考(管家)基因进行样本间标准化。在这里,我们提出了一种新的标准化方法,即去除不需要的变异-III(RUV-III),该方法充分利用了技术重复和合适的对照基因。当没有技术重复时,我们还提出了一种使用伪重复的方法。RUV-III 在四个不同的数据集上得到了验证。我们还就涉及该技术的研究的设计和分析提供了建议。