Linear mixed models for association analysis of quantitative traits with next-generation sequencing data

被引:4
作者
Chiu, Chi-yang [1 ,2 ]
Yuan, Fang [3 ]
Zhang, Bingsong [4 ]
Yuan, Ao [4 ]
Li, Xin [4 ]
Fang, Hong-Bin [4 ]
Lange, Kenneth [5 ]
Weeks, Daniel E. [6 ,7 ]
Wilson, Alexander F. [2 ]
Bailey-Wilson, Joan E. [2 ]
Musolf, Anthony M. [2 ]
Stambolian, Dwight [8 ]
Lakhal-Chaieb, M'Hamed Lajmi [9 ]
Cook, Richard J. [10 ]
McMahon, Francis J. [11 ,12 ]
Amos, Christopher I. [13 ]
Xiong, Momiao [14 ]
Fan, Ruzong [2 ,4 ]
机构
[1] Univ Tennessee, Hlth Sci Ctr, Div Biostat, Dept Prevent Med, Memphis, TN USA
[2] NHGRI, Computat & Stat Genom Branch, NIH, Bethesda, MD 20892 USA
[3] Kunming Med Univ, Sch Basic Med, Dept Biochem & Mol Biol, Kunming, Yunnan, Peoples R China
[4] Georgetown Univ, Med Ctr, Dept Biostat Bioinformat & Biomath, 4000 Reservoir Rd NW,Bldg D-180, Washington, DC 20057 USA
[5] Univ Calif Los Angeles, David Geffen Sch Med, Dept Human Genet, Los Angeles, CA 90095 USA
[6] Univ Pittsburgh, Grad Sch Publ Hlth, Dept Biostat, Pittsburgh, PA 15261 USA
[7] Univ Pittsburgh, Grad Sch Publ Hlth, Dept Human Genet, Pittsburgh, PA 15261 USA
[8] Univ Penn, Dept Genet, Philadelphia, PA 19104 USA
[9] Univ Laval, Dept Math & Stat, Quebec City, PQ, Canada
[10] Univ Waterloo, Dept Stat & Actuarial Sci, Waterloo, ON, Canada
[11] NIMH, Human Genet Branch, NIH, Bethesda, MD 20892 USA
[12] NIMH, Genet Basis Mood & Anxiety Disorders Sect, NIH, Bethesda, MD 20892 USA
[13] Baylor Coll Med, Dept Med, Houston, TX 77030 USA
[14] Univ Texas Houston, Human Genet Ctr, Houston, TX USA
基金
美国国家卫生研究院;
关键词
common variants; complex diseases; functional data analysis; functional linear mixed models; linear mixed models; rare variants; COMMON DISEASES; RARE VARIANTS; LINKAGE; MYOPIA;
D O I
10.1002/gepi.22177
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We develop linear mixed models (LMMs) and functional linear mixed models (FLMMs) for gene-based tests of association between a quantitative trait and genetic variants on pedigrees. The effects of a major gene are modeled as a fixed effect, the contributions of polygenes are modeled as a random effect, and the correlations of pedigree members are modeled via inbreeding/ kinship coefficients. F-statistics and. 2 likelihood ratio test (LRT) statistics based on the LMMs and FLMMs are constructed to test for association. We show empirically that the F-distributed statistics provide a good control of the type I error rate. The F-test statistics of the LMMs have similar or higher power than the FLMMs, kernel-based famSKAT (family-based sequence kernel association test), and burden test famBT (family-based burden test). The F-statistics of the FLMMs perform well when analyzing a combination of rare and common variants. For small samples, the LRT statistics of the FLMMs control the type I error rate well at the nominal levels alpha = 0.01 and 0.05. For moderate/ large samples, the LRT statistics of the FLMMs control the type I error rates well. The LRT statistics of the LMMs can lead to inflated type I error rates. The proposed models are useful in whole genome and whole exome association studies of complex traits.
引用
收藏
页码:189 / 206
页数:18
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