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Probe set filtering increases correlation between Affymetrix GeneChip and qRT-PCR expression measurements

机译:探针组过滤可提高Affymetrix基因芯片与qRT-PCR表达测量之间的相关性

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Background Affymetrix GeneChip microarrays are popular platforms for expression profiling in two types of studies: detection of differential expression computed by p-values of t -test and estimation of fold change between analyzed groups. There are many different preprocessing algorithms for summarizing Affymetrix data. The main goal of these methods is to remove effects of non-specific hybridization, and to optimally combine information from multiple probes annotated to the same transcript. The methods are benchmarked by comparison with reference methods, such as quantitative reverse-transcription PCR (qRT-PCR). Results We present a comprehensive analysis of agreement between Affymetrix GeneChip and qRT-PCR results. We analyzed the influence of filtering by fraction Present calls introduced by J.N. McClintick and H.J. Edenberg (2006) and 2 mapping procedures: updated probe sets definitions proposed by Dai et al. (2005) and our "naive mapping" method. Because of evolution of genome sequence annotations since the time when microarrays were designed, we also studied the effect of the annotation release date. These comparisons were prepared for 6 popular preprocessing algorithms (MAS5, PLIER, RMA, GC-RMA, MBEI, and MBEImm) in the 2 above-mentioned types of studies. We used data sets from 6 independent biological experiments. As a measure of reproducibility of microarray and qRT-PCR values, we used linear and rank correlation coefficients. Conclusions We show that filtering by fraction Present calls increased correlations for all 6 preprocessing algorithms. We observed the difference in performance of PM-MM and PM-only methods: using MM probes increased correlations in fold change studies, but PM-only methods proved to perform better in detection of differential expression. We recommend using GC-RMA for detection of differential expression and PLIER for estimation of fold change. The use of the more recent annotation improves the results in both types of studies, encouraging re-analysis of old data.
机译:背景Affymetrix GeneChip微阵列是在两种类型的研究中进行表达谱分析的流行平台:检测由t检验的p值计算的差异表达,以及估计分析组之间的倍数变化。有许多不同的预处理算法可用于汇总Affymetrix数据。这些方法的主要目标是消除非特异性杂交的影响,并以最佳方式组合来自多个标注有相同转录本的探针的信息。通过与参考方法(例如定量逆转录PCR(qRT-PCR))进行比较来对这些方法进行基准测试。结果我们对Affymetrix基因芯片与qRT-PCR结果之间的一致性进行了全面分析。我们分析了由J.N. McClintick和H.J. Edenberg(2006)和2种作图程序:Dai等人提出的更新的探针集定义。 (2005)和我们的“幼稚映射”方法。自从设计微阵列以来,由于基因组序列注释的演变,我们还研究了注释发布日期的影响。这些比较是针对上述两种研究类型中的6种流行的预处理算法(MAS5,PLIER,RMA,GC-RMA,MBEI和MBEImm)进行的。我们使用了来自6个独立生物学实验的数据集。为了衡量微阵列和qRT-PCR值的可重复性,我们使用了线性和秩相关系数。结论我们表明,按分数Present进行过滤会提高所有6种预处理算法的相关性。我们观察到了PM-MM和仅PM方法的性能差异:使用MM探针在倍数变化研究中增加了相关性,但事实证明,仅PM方法在检测差异表达方面表现更好。我们建议使用GC-RMA来检测差异表达,并使用PLIER来估计倍数变化。使用较新的注释可以改善两种研究的结果,并鼓励对旧数据进行重新分析。

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