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Qvalue methods may not always control false discovery rate in genomic applications

机译:Qvalue方法可能无法始终控制基因组应用程序中的错误发现率

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The qvalue method by Storey (2002, 2003) has been proved to be theoretically sound for controlling false discovery rate in many high throughput genomic applications. However, empirical evidences suggest that this method can be more stringent than other methods, such as Bonferroni adjustment and the FDR method by Benjamini and Hochberg (1995). We compare these methods for detection of gene differential expression in microarray data analysis. For microarray experiment with the purpose of gene discovery, where many genes are expected to be differentially expressed across different experimental conditions, the qvalue method generally performs well. However, for experiments with only a few genes expected to be differentially expressed, the qvalue method performs much worse than other methods. Some insights are provided to examine this discrepancy. Adjustments to q-value method are recommended to accommodate many applications.
机译:Storey(2002,2003)的qvalue方法已被证明在许多高通量基因组应用中用于控制错误发现率在理论上是合理的。但是,经验证据表明,该方法可能比其他方法更为严格,例如Benjamini和Hochberg(1995)的Bonferroni调整和FDR方法。我们比较了这些方法在微阵列数据分析中检测基因差异表达的方法。对于以基因发现为目的的微阵列实验,预计许多基因会在不同的实验条件下差异表达,因此qvalue方法通常表现良好。但是,对于只有少数几个基因有望被差异表达的实验,qvalue方法的性能要比其他方法差很多。提供了一些见解来检查这种差异。建议调整q值方法以适应许多应用。

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