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A Bayesian approach to efficient differential allocation for resampling-based significance testing

机译:基于重采采样的重要性测试的高效差分分配的贝叶斯方法

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Background Large-scale statistical analyses have become hallmarks of post-genomic era biological research due to advances in high-throughput assays and the integration of large biological databases. One accompanying issue is the simultaneous estimation of p-values for a large number of hypothesis tests. In many applications, a parametric assumption in the null distribution such as normality may be unreasonable, and resampling-based p-values are the preferred procedure for establishing statistical significance. Using resampling-based procedures for multiple testing is computationally intensive and typically requires large numbers of resamples. Results We present a new approach to more efficiently assign resamples (such as bootstrap samples or permutations) within a nonparametric multiple testing framework. We formulated a Bayesian-inspired approach to this problem, and devised an algorithm that adapts the assignment of resamples iteratively with negligible space and running time overhead. In two experimental studies, a breast cancer microarray dataset and a genome wide association study dataset for Parkinson's disease, we demonstrated that our differential allocation procedure is substantially more accurate compared to the traditional uniform resample allocation. Conclusion Our experiments demonstrate that using a more sophisticated allocation strategy can improve our inference for hypothesis testing without a drastic increase in the amount of computation on randomized data. Moreover, we gain more improvement in efficiency when the number of tests is large. R code for our algorithm and the shortcut method are available at http://people.pcbi.upenn.edu/~lswang/pub/bmc2009/ .
机译:背景技术由于高通量测定的进展以及大型生物数据库的整合,大规模统计分析已成为基因组后生物学研究的标志。一个随附的问题是同时估计大量假设试验的p值。在许多应用中,诸如正常性的空分布中的参数假设可能是不合理的,并且基于重采样的p值是用于建立统计显着性的优选过程。使用基于重采样的多个测试程序是计算密集的,通常需要大量的重建。结果我们提出了一种新方法,可以在非参数多个测试框架内更有效地将重建(例如引导样本或置换)进行更有效地分配。我们制定了贝叶斯激发了这个问题的启发方法,并设计了一种算法,它适应迭代的差分分配,空间和运行时间开销。在两项实验研究中,乳腺癌微阵列数据集和帕金森病的基因组宽协会研究数据集,我们证明了与传统的统一重组分配相比,我们的差分分配程序基本上更准确。结论我们的实验表明,使用更复杂的分配策略可以改善我们对假设测试的推断,而无需随机数据的计算量的急剧增加。此外,当测试数量大时,我们提高了更高的效率。我们的算法和快捷方式方法的R代码可在http://people.pcbi.upenn.edu/~lswang/pub/bmc2009/获取。

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