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首页> 外文期刊>Open Journal of Statistics >Genome-Wide Likelihood Ratio Tests under Heterogeneity
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Genome-Wide Likelihood Ratio Tests under Heterogeneity

机译:异质性下的全基因组可能性比检验

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摘要

The commonly used statistical methods in medical research generally assume patients arise from one homogeneous population. However, the existence and importance of significant heterogeneity have been widely documented. It is well known that common and complex human diseases usually have heterogeneous disease etiology, which often involves interplay of multiple genetic and environmental factors, leading to latent population substructure. Genome-wide association studies (GWAS) is a useful tool to uncover genetic association with disease of interest, while linkage analysis is a commonly used method to identify statistical association between the inheritance of a human disease and inheritance of marker loci that are in linkage with disease causing loci. We propose a likelihood ratio test for genome-wide linkage analysis under genetic heterogeneity using family data. We derive a closed-form formula for the LRT test statistic and provide explicit asymptotic null distribution. The closed form asymptotic distribution allows easy determination of the asymptotic p-values. Our extensive simulation studies indicate that the proposed test has proper type I error and good power under genetic heterogeneity. In order to simplify application of the proposed method for non-statisticians, we develop an R package gLRTH to implement the proposed LRT for genome-wide linkage analysis as well as Qian and Shao’s LRT for GWAS under heterogeneity. The newly developed open source R package gLRTH is available at CRAN.
机译:医学研究中常用的统计方法通常假定患者来自一个同质人群。但是,大量异质性的存在和重要性已被广泛记录。众所周知,常见和复杂的人类疾病通常具有异质的病因,通常涉及多种遗传和环境因素的相互作用,导致潜在的人口亚结构。全基因组关联研究(GWAS)是揭示与所关注疾病的遗传关联的有用工具,而连锁分析则是鉴定人类疾病遗传与与之关联的标记基因座遗传之间统计关联的常用方法。引起疾病的位点。我们提出了使用家族数据进行遗传异质性下全基因组连锁分析的似然比检验。我们为LRT测试统计量导出一个封闭式公式,并提供显式渐近零分布。闭合形式的渐近分布允许轻松确定渐近p值。我们广泛的仿真研究表明,所提出的测试在遗传异质性下具有适当的I型错误和良好的功效。为了简化所提出​​的方法在非统计学家中的应用,我们开发了R包gLRTH来实现拟议的LRT用于全基因组连锁分析,以及Qian和Shao的LRT用于GWAS的异质性。新开发的开源R包gLRTH可在CRAN获得。

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