...
首页> 外文期刊>Bioinformatics >Quick calculation for sample size while controlling false discovery rate with application to microarray analysis
【24h】

Quick calculation for sample size while controlling false discovery rate with application to microarray analysis

机译:快速计算样品量,同时控制错误发现率,并将其应用于微阵列分析

获取原文
获取原文并翻译 | 示例
           

摘要

Motivation: Sample size calculation is important in experimental design and is even more so in microarray or proteomic experiments since only a few repetitions can be afforded. In the multiple testing problems involving these experiments, it is more powerful and more reasonable to control false discovery rate (FDR) or positive FDR (pFDR) instead of type I error, e.g. family-wise error rate (FWER). When controlling FDR, the traditional approach of estimating sample size by controlling type I error is no longer applicable. Results: Our proposed method applies to controlling FDR. The sample size calculation is straightforward and requires minimal computation, as illustrated with two sample t-tests and F-tests. Based on simulation with the resultant sample size, the power is shown to be achievable by the q-value procedure. Availability: A Matlab code implementing the described methods is available upon request. Contact: pliu@iastate.edu Supplementary information: Supplementary data are available at Bioinformatics online.
机译:动机:样本量的计算在实验设计中很重要,在微阵列或蛋白质组学实验中更是如此,因为只能进行几次重复。在涉及这些实验的多种测试问题中,控制错误发现率(FDR)或正FDR(pFDR)代替I型错误(例如I型错误)更加有效和合理。家庭错误率(FWER)。当控制FDR时,通过控制I型错误来估计样本量的传统方法不再适用。结果:我们提出的方法适用于控制FDR。样本数量的计算非常简单,并且需要最少的计算,如两个样本t检验和F检验所示。基于结果样本大小的仿真,表明功率可以通过q值过程获得。可用性:可根据要求提供实现所描述方法的Matlab代码。联系人:pliu@iastate.edu补充信息:补充数据可从Bioinformatics在线获得。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号