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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.
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篇名 Genome-Wide Likelihood Ratio Tests under Heterogeneity
来源期刊 统计学期刊(英文) 学科 医学
关键词 GENETIC HETEROGENEITY Transmission HETEROGENEITY Complex Disease GENOME-WIDE ASSOCIATION Study GENETIC LINKAGE Analysis R Software PACKAGE
年,卷(期) 2018,(3) 所属期刊栏目
研究方向 页码范围 468-478
页数 11页 分类号 R73
字数 语种
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GENETIC
HETEROGENEITY
Transmission
HETEROGENEITY
Complex
Disease
GENOME-WIDE
ASSOCIATION
Study
GENETIC
LINKAGE
Analysis
R
Software
PACKAGE
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研究来源
研究分支
研究去脉
引文网络交叉学科
相关学者/机构
期刊影响力
统计学期刊(英文)
半月刊
2161-718X
武汉市江夏区汤逊湖北路38号光谷总部空间
出版文献量(篇)
584
总下载数(次)
0
总被引数(次)
0
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