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Comparison of analyses of the QTLMAS XII common dataset. II: genome-wide association and fine mapping.QTLMAS XII公共数据集分析的比较。II:全基因组关联分析和精细定位。
BMC Proc. 2009 Feb 23;3 Suppl 1(Suppl 1):S2. doi: 10.1186/1753-6561-3-s1-s2.
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Bayesian variable and model selection methods for genetic association studies.用于基因关联研究的贝叶斯变量与模型选择方法。
Genet Epidemiol. 2009 Jan;33(1):27-37. doi: 10.1002/gepi.20353.
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Statistical Methods for Mapping Multiple QTL.多位点数量性状基因座定位的统计方法
Int J Plant Genomics. 2008;2008:286561. doi: 10.1155/2008/286561.
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Breeding designs for recombinant inbred advanced intercross lines.重组自交高级互交系的育种设计。
Genetics. 2008 Jun;179(2):1069-78. doi: 10.1534/genetics.107.083873. Epub 2008 May 27.
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Naive application of permutation testing leads to inflated type I error rates.单纯应用置换检验会导致第一类错误率膨胀。
Genetics. 2008 Jan;178(1):609-10. doi: 10.1534/genetics.107.074609.
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Quantifying evidence for candidate gene polymorphisms: Bayesian analysis combining sequence-specific and quantitative trait loci colocation information.量化候选基因多态性的证据:结合序列特异性和数量性状基因座共定位信息的贝叶斯分析。
Genetics. 2007 Dec;177(4):2399-416. doi: 10.1534/genetics.106.069955.
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WOMBAT: a tool for mixed model analyses in quantitative genetics by restricted maximum likelihood (REML).WOMBAT:一种通过限制最大似然法(REML)进行数量遗传学混合模型分析的工具。
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A validated whole-genome association study of efficient food conversion in cattle.一项经过验证的牛高效食物转化全基因组关联研究。
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基于重采样模型平均的结构群体映射。

Mapping in structured populations by resample model averaging.

机构信息

Wellcome Trust Centre for Human Genetics, Roosevelt Dr., Oxford OX3 7BN, United Kingdom.

出版信息

Genetics. 2009 Aug;182(4):1263-77. doi: 10.1534/genetics.109.100727. Epub 2009 May 27.

DOI:10.1534/genetics.109.100727
PMID:19474203
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2728864/
Abstract

Highly recombinant populations derived from inbred lines, such as advanced intercross lines and heterogeneous stocks, can be used to map loci far more accurately than is possible with standard intercrosses. However, the varying degrees of relatedness that exist between individuals complicate analysis, potentially leading to many false positive signals. We describe a method to deal with these problems that does not require pedigree information and accounts for model uncertainty through model averaging. In our method, we select multiple quantitative trait loci (QTL) models using forward selection applied to resampled data sets obtained by nonparametric bootstrapping and subsampling. We provide model-averaged statistics about the probability of loci or of multilocus regions being included in model selection, and this leads to more accurate identification of QTL than by single-locus mapping. The generality of our approach means it can potentially be applied to any population of unknown structure.

摘要

高度重组的种群来源于近交系,如高级互交系和异质群体,可以比标准互交更准确地定位基因座。然而,个体之间存在的不同程度的亲缘关系使分析变得复杂,可能导致许多假阳性信号。我们描述了一种不需要系谱信息的方法,并通过模型平均来处理模型不确定性。在我们的方法中,我们使用向前选择选择多个数量性状基因座(QTL)模型,向前选择应用于通过非参数引导抽样和抽样获得的重采样数据集。我们提供了关于基因座或多基因座区域被模型选择包括的概率的模型平均统计信息,这比单基因座映射更能准确地识别 QTL。我们方法的通用性意味着它可能适用于任何未知结构的群体。