Yuan Joshua S, Reed Ann, Chen Feng, Stewart C Neal
Department of Plant Sciences, University of Tennessee, Knoxville, TN 37996, USA.
BMC Bioinformatics. 2006 Feb 22;7:85. doi: 10.1186/1471-2105-7-85.
Even though real-time PCR has been broadly applied in biomedical sciences, data processing procedures for the analysis of quantitative real-time PCR are still lacking; specifically in the realm of appropriate statistical treatment. Confidence interval and statistical significance considerations are not explicit in many of the current data analysis approaches. Based on the standard curve method and other useful data analysis methods, we present and compare four statistical approaches and models for the analysis of real-time PCR data.
In the first approach, a multiple regression analysis model was developed to derive DeltaDeltaCt from estimation of interaction of gene and treatment effects. In the second approach, an ANCOVA (analysis of covariance) model was proposed, and the DeltaDeltaCt can be derived from analysis of effects of variables. The other two models involve calculation DeltaCt followed by a two group t-test and non-parametric analogous Wilcoxon test. SAS programs were developed for all four models and data output for analysis of a sample set are presented. In addition, a data quality control model was developed and implemented using SAS.
Practical statistical solutions with SAS programs were developed for real-time PCR data and a sample dataset was analyzed with the SAS programs. The analysis using the various models and programs yielded similar results. Data quality control and analysis procedures presented here provide statistical elements for the estimation of the relative expression of genes using real-time PCR.
尽管实时定量聚合酶链反应(real-time PCR)已在生物医学领域广泛应用,但用于分析定量实时PCR的数据处理程序仍然缺乏;特别是在适当的统计处理方面。在当前许多数据分析方法中,置信区间和统计显著性的考量并不明确。基于标准曲线法和其他有用的数据分析方法,我们提出并比较了四种用于分析实时PCR数据的统计方法和模型。
在第一种方法中,开发了一个多元回归分析模型,通过估计基因与处理效应的相互作用来推导ΔΔCt。在第二种方法中,提出了一个协方差分析(ANCOVA)模型,ΔΔCt可通过变量效应分析得出。另外两种模型涉及先计算ΔCt,然后进行两组t检验和非参数类似的Wilcoxon检验。为所有四种模型开发了SAS程序,并展示了用于分析样本集的数据输出。此外,使用SAS开发并实施了一个数据质量控制模型。
针对实时PCR数据开发了带有SAS程序的实用统计解决方案,并使用SAS程序分析了一个样本数据集。使用各种模型和程序进行的分析产生了相似的结果。这里介绍的数据质量控制和分析程序为使用实时PCR估计基因相对表达提供了统计要素。