首页> 外文期刊>Genetics: A Periodical Record of Investigations Bearing on Heredity and Variation >Rapid and Robust Resampling-Based Multiple-Testing Correction with Application in a Genome-Wide Expression Quantitative Trait Loci Study
【24h】

Rapid and Robust Resampling-Based Multiple-Testing Correction with Application in a Genome-Wide Expression Quantitative Trait Loci Study

机译:基于快速和稳健的基于重采样的多重测试校正及其在基因组范围内表达定量性状位点研究中的应用

获取原文
获取原文并翻译 | 示例
           

摘要

Genome-wide expression quantitative trait loci (eQTL) studies have emerged as a powerful tool to understand the genetic basis of gene expression and complex traits. In a typical eQTL study, the huge number of genetic markers and expression traits and their complicated correlations present a challenging multiple-testing correction problem. The resampling-based test using permutation or bootstrap procedures is a standard approach to address the multiple-testing problem in eQTL studies. A brute force application of the resampling-based test to large-scale eQTL data sets is often computationally infeasible. Several computationally efficient methods have been proposed to calculate approximate resampling-based P-values. However, these methods rely on certain assumptions about the correlation structure of the genetic markers, which may not be valid for certain studies. We propose a novel algorithm, rapid and exact multiple testing correction by resampling (REM), to address this challenge. REM calculates the exact resampling-based P-values in a computationally efficient manner. The computational advantage of REM lies in its strategy of pruning the search space by skipping genetic markers whose upper bounds on test statistics are small. REM does not rely on any assumption about the correlation structure of the genetic markers. It can be applied to a variety of resampling-based multiple-testing correction methods including permutation and bootstrap methods. We evaluate REM on three eQTL data sets (yeast, inbred mouse, and human rare variants) and show that it achieves accurate resampling-based P-value estimation with much less computational cost than existing methods. The software is available at http://csbio.unc.edu/eQTL.
机译:全基因组表达定量性状基因座(eQTL)研究已成为了解基因表达和复杂性状遗传基础的有力工具。在一项典型的eQTL研究中,大量的遗传标记和表达特征及其复杂的相关性提出了具有挑战性的多重测试校正问题。使用置换或引导程序的基于重采样的测试是解决eQTL研究中的多重测试问题的标准方法。将基于重采样的测试强行应用于大规模eQTL数据集通常在计算上是不可行的。已经提出了几种计算上有效的方法来计算基于近似重采样的P值。但是,这些方法依赖于有关遗传标记相关结构的某些假设,对于某些研究可能无效。我们提出了一种新颖的算法,即通过重新采样(REM)进行快速准确的多次测试校正,以解决这一挑战。 REM以计算有效的方式计算基于精确重采样的P值。 REM的计算优势在于它通过跳过测试统计量上限较小的遗传标记来修剪搜索空间的策略。 REM不依赖于关于遗传标记的相关结构的任何假设。它可以应用于多种基于重采样的多重测试校正方法,包括置换和自举方法。我们在三个eQTL数据集(酵母,近交小鼠和人类稀有变体)上评估了REM,并显示与现有方法相比,它可以实现精确的基于重采样的P值估算,且计算成本低得多。该软件可从http://csbio.unc.edu/eQTL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