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TreeQTL: hierarchical error control for eQTL findings.TreeQTL:eQTL研究结果的分层错误控制
Bioinformatics. 2016 Aug 15;32(16):2556-8. doi: 10.1093/bioinformatics/btw198. Epub 2016 Apr 19.
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Fast and efficient QTL mapper for thousands of molecular phenotypes.适用于数千种分子表型的快速高效QTL定位器。
Bioinformatics. 2016 May 15;32(10):1479-85. doi: 10.1093/bioinformatics/btv722. Epub 2015 Dec 26.
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Accurate and fast multiple-testing correction in eQTL studies.在全基因组关联研究中进行准确快速的多重检验校正。
Am J Hum Genet. 2015 Jun 4;96(6):857-68. doi: 10.1016/j.ajhg.2015.04.012. Epub 2015 May 28.
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Human genomics. The Genotype-Tissue Expression (GTEx) pilot analysis: multitissue gene regulation in humans.人类基因组学。基因型-组织表达(GTEx)试点分析:人类多组织基因调控
Science. 2015 May 8;348(6235):648-60. doi: 10.1126/science.1262110. Epub 2015 May 7.
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HTSeq--a Python framework to work with high-throughput sequencing data.HTSeq——一个用于处理高通量测序数据的Python框架。
Bioinformatics. 2015 Jan 15;31(2):166-9. doi: 10.1093/bioinformatics/btu638. Epub 2014 Sep 25.
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The relevance of HLA sequencing in population genetics studies.HLA 测序在群体遗传学研究中的相关性。
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9
Transcriptome and genome sequencing uncovers functional variation in humans.转录组和基因组测序揭示了人类功能变异。
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The UCSC genome browser and associated tools.UCSC 基因组浏览器及相关工具。
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一种考虑变体间连锁不平衡的eQTL研究的高效多重检验调整方法。

An Efficient Multiple-Testing Adjustment for eQTL Studies that Accounts for Linkage Disequilibrium between Variants.

作者信息

Davis Joe R, Fresard Laure, Knowles David A, Pala Mauro, Bustamante Carlos D, Battle Alexis, Montgomery Stephen B

机构信息

Department of Genetics, Stanford University, Stanford, CA 94305, USA.

Department of Pathology, Stanford University, Stanford, CA 94305, USA.

出版信息

Am J Hum Genet. 2016 Jan 7;98(1):216-24. doi: 10.1016/j.ajhg.2015.11.021. Epub 2015 Dec 31.

DOI:10.1016/j.ajhg.2015.11.021
PMID:26749306
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4716687/
Abstract

Methods for multiple-testing correction in local expression quantitative trait locus (cis-eQTL) studies are a trade-off between statistical power and computational efficiency. Bonferroni correction, though computationally trivial, is overly conservative and fails to account for linkage disequilibrium between variants. Permutation-based methods are more powerful, though computationally far more intensive. We present an alternative correction method called eigenMT, which runs over 500 times faster than permutations and has adjusted p values that closely approximate empirical ones. To achieve this speed while also maintaining the accuracy of permutation-based methods, we estimate the effective number of independent variants tested for association with a particular gene, termed Meff, by using the eigenvalue decomposition of the genotype correlation matrix. We employ a regularized estimator of the correlation matrix to ensure Meff is robust and yields adjusted p values that closely approximate p values from permutations. Finally, using a common genotype matrix, we show that eigenMT can be applied with even greater efficiency to studies across tissues or conditions. Our method provides a simpler, more efficient approach to multiple-testing correction than existing methods and fits within existing pipelines for eQTL discovery.

摘要

在局部表达数量性状基因座(顺式eQTL)研究中进行多重检验校正的方法是统计功效和计算效率之间的权衡。Bonferroni校正虽然计算简单,但过于保守,且未考虑变异之间的连锁不平衡。基于置换的方法功效更强,不过计算强度要大得多。我们提出了一种名为eigenMT的替代校正方法,其运行速度比置换方法快500多倍,且调整后的p值与经验p值非常接近。为了在实现这种速度的同时还能保持基于置换方法的准确性,我们通过使用基因型相关矩阵的特征值分解来估计与特定基因关联测试的独立变异的有效数量,即Meff。我们采用相关矩阵的正则化估计器来确保Meff稳健,并产生与置换得到的p值非常接近的调整后p值。最后,使用一个常见的基因型矩阵,我们表明eigenMT可以更高效地应用于跨组织或条件的研究。我们的方法为多重检验校正提供了一种比现有方法更简单、更高效的途径,并且适合现有的eQTL发现流程。