Significance test and genome selection in bayesian shrinkage analysis.

International journal of plant genomics Pub Date : 2010-01-01 Epub Date: 2010-06-10 DOI:10.1155/2010/893206
Xiaohong Che, Shizhong Xu
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引用次数: 45

Abstract

Bayesian shrinkage analysis is the state-of-the-art method for whole genome analysis of quantitative traits. It can estimate the genetic effects for the entire genome using a dense marker map. The technique is now called genome selection. A nice property of the shrinkage analysis is that it can estimate effects of QTL as small as explaining 2% of the phenotypic variance in a typical sample size of 300-500 individuals. In most cases, QTL can be detected with simple visual inspection of the entire genome for the effect because the false positive rate is low. As a Bayesian method, no significance test is needed. However, it is still desirable to put some confidences on the estimated QTL effects. We proposed to use the permutation test to draw empirical thresholds to declare significance of QTL under a predetermined genome wide type I error. With the permutation test, Bayesian shrinkage analysis can be routinely used for QTL detection.

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贝叶斯收缩分析的显著性检验和基因组选择。
贝叶斯收缩分析是最先进的全基因组数量性状分析方法。它可以利用密集的标记图谱来估计整个基因组的遗传效应。这项技术现在被称为基因组选择。收缩分析的一个很好的特性是,它可以估计QTL的影响,在300-500个个体的典型样本量中,它可以解释2%的表型差异。在大多数情况下,QTL可以通过对整个基因组的简单目视检查来检测,因为假阳性率很低。作为贝叶斯方法,不需要显著性检验。然而,对估计的QTL效应有一定的信心仍然是可取的。我们建议使用排列检验来绘制经验阈值,以声明QTL在预定的全基因组I型误差下的显著性。有了排列检验,贝叶斯收缩分析可以常规用于QTL检测。
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