Wang Huixia, He Xuming
Department of Statistics, North Carolina State University, Raleigh, North Carolina 27695, USA.
Biometrics. 2008 Jun;64(2):449-57. doi: 10.1111/j.1541-0420.2007.00903.x. Epub 2008 Mar 5.
Due to the small number of replicates in typical gene microarray experiments, the performance of statistical inference is often unsatisfactory without some form of information-sharing across genes. In this article, we propose an enhanced quantile rank score test (EQRS) for detecting differential expression in GeneChip studies by analyzing the quantiles of gene intensity distributions through probe-level measurements. A measure of sign correlation, delta, plays an important role in the rank score tests. By sharing information across genes, we develop a calibrated estimate of delta, which reduces the variability at small sample sizes. We compare the EQRS test with four other approaches for determining differential expression: the gene-specific quantile rank score test, the quantile rank score test assuming a common delta, a modified t-test using summarized probe-set-level intensities, and the Mack-Skillings rank test on probe-level data. The proposed EQRS is shown to be favorable for preserving false discovery rates and for being robust against outlying arrays. In addition, we demonstrate the merits of the proposed approach using a GeneChip study comparing gene expression in the livers of mice exposed to chronic intermittent hypoxia and of those exposed to intermittent room air.
由于典型基因微阵列实验中的重复样本数量较少,若不进行某种形式的基因间信息共享,统计推断的性能往往不尽人意。在本文中,我们提出了一种增强分位数秩得分检验(EQRS),通过探针水平测量分析基因强度分布的分位数,以检测基因芯片研究中的差异表达。符号相关性度量delta在秩得分检验中起着重要作用。通过跨基因共享信息,我们开发了一种delta的校准估计方法,该方法减少了小样本量时的变异性。我们将EQRS检验与其他四种确定差异表达的方法进行了比较:基因特异性分位数秩得分检验、假设共同delta的分位数秩得分检验、使用汇总探针集水平强度的修正t检验以及基于探针水平数据的Mack-Skillings秩检验。结果表明,所提出的EQRS在控制错误发现率和抵御异常阵列方面具有优势。此外,我们通过一项基因芯片研究展示了该方法的优点,该研究比较了暴露于慢性间歇性缺氧的小鼠肝脏与暴露于间歇性室内空气的小鼠肝脏中的基因表达。