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一种利用来自相关基因组扫描的信息在数量性状基因座分析中更新推断的经验贝叶斯方法。

An empirical Bayes method for updating inferences in analysis of quantitative trait loci using information from related genome scans.

作者信息

Zhang Kui, Wiener Howard, Beasley Mark, George Varghese, Amos Christopher I, Allison David B

机构信息

Department of Biostatistics, Section of Statistical Genetics, University of Alabama, Birmingham 35294, USA.

出版信息

Genetics. 2006 Aug;173(4):2283-96. doi: 10.1534/genetics.106.057448. Epub 2006 Jun 4.

Abstract

Individual genome scans for quantitative trait loci (QTL) mapping often suffer from low statistical power and imprecise estimates of QTL location and effect. This lack of precision yields large confidence intervals for QTL location, which are problematic for subsequent fine mapping and positional cloning. In prioritizing areas for follow-up after an initial genome scan and in evaluating the credibility of apparent linkage signals, investigators typically examine the results of other genome scans of the same phenotype and informally update their beliefs about which linkage signals in their scan most merit confidence and follow-up via a subjective-intuitive integration approach. A method that acknowledges the wisdom of this general paradigm but formally borrows information from other scans to increase confidence in objectivity would be a benefit. We developed an empirical Bayes analytic method to integrate information from multiple genome scans. The linkage statistic obtained from a single genome scan study is updated by incorporating statistics from other genome scans as prior information. This technique does not require that all studies have an identical marker map or a common estimated QTL effect. The updated linkage statistic can then be used for the estimation of QTL location and effect. We evaluate the performance of our method by using extensive simulations based on actual marker spacing and allele frequencies from available data. Results indicate that the empirical Bayes method can account for between-study heterogeneity, estimate the QTL location and effect more precisely, and provide narrower confidence intervals than results from any single individual study. We also compared the empirical Bayes method with a method originally developed for meta-analysis (a closely related but distinct purpose). In the face of marked heterogeneity among studies, the empirical Bayes method outperforms the comparator.

摘要

针对数量性状基因座(QTL)定位的个体基因组扫描常常存在统计功效低以及QTL位置和效应估计不精确的问题。这种缺乏精确性导致QTL位置的置信区间很大,这对于后续的精细定位和位置克隆来说是个难题。在初次基因组扫描后对后续跟进区域进行优先级排序以及评估明显连锁信号的可信度时,研究人员通常会检查相同表型的其他基因组扫描结果,并通过主观直观的整合方法非正式地更新他们对于自身扫描中哪些连锁信号最值得置信和跟进的看法。一种认可这种一般范式的合理性但正式借鉴其他扫描信息以增强客观性置信度的方法会很有益处。我们开发了一种经验贝叶斯分析方法来整合来自多个基因组扫描的信息。通过将来自其他基因组扫描的统计数据作为先验信息纳入,对从单个基因组扫描研究中获得的连锁统计量进行更新。该技术并不要求所有研究具有相同的标记图谱或共同的估计QTL效应。然后,更新后的连锁统计量可用于估计QTL的位置和效应。我们基于可用数据中的实际标记间距和等位基因频率,通过广泛的模拟来评估我们方法的性能。结果表明,经验贝叶斯方法能够考虑研究间的异质性,更精确地估计QTL位置和效应,并且提供比任何单个单独研究结果更窄的置信区间。我们还将经验贝叶斯方法与最初为荟萃分析开发的一种方法(目的密切相关但不同)进行了比较。在研究间存在显著异质性的情况下,经验贝叶斯方法优于比较方法。

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本文引用的文献

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