Joint Analysis of Multiple Traits in Rare Variant Association Studies

被引:12
|
作者
Wang, Zhenchuan [1 ]
Wang, Xuexia [2 ]
Sha, Qiuying [1 ]
Zhang, Shuanglin [1 ]
机构
[1] Michigan Technol Univ, Dept Math Sci, 1400 Townsend Dr, Houghton, MI 49931 USA
[2] Univ Wisconsin, Joseph J Zilber Sch Publ Hlth, Milwaukee, WI 53201 USA
关键词
Rare variants; multiple traits; association studies; multiple correlated phenotypes; pleiotropy; PRINCIPAL-COMPONENTS; DETECTING ASSOCIATION; GENETIC ASSOCIATION; SEMIPARAMETRIC TEST; COMMON DISEASES; GENOMIC CONTROL; MODEL APPROACH; SEQUENCE; PLEIOTROPY; STRATIFICATION;
D O I
10.1111/ahg.12149
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The joint analysis of multiple traits has recently become popular since it can increase statistical power to detect genetic variants and there is increasing evidence showing that pleiotropy is a widespread phenomenon in complex diseases. Currently, the majority of existing methods for the joint analysis of multiple traits test association between one common variant and multiple traits. However, the variant-by-variant methods for common variant association studies may not be optimal for rare variant association studies due to the allelic heterogeneity as well as the extreme rarity of individual variants. Current statistical methods for rare variant association studies are for one single trait only. In this paper, we propose an adaptive weighting reverse regression (AWRR) method to test association between multiple traits and rare variants in a genomic region. AWRR is robust to the directions of effects of causal variants and is also robust to the directions of association of traits. Using extensive simulation studies, we compare the performance of AWRR with canonical correlation analysis (CCA), Single-TOW, and the weighted sum reverse regression (WSRR). Our results show that, in all of the simulation scenarios, AWRR is consistently more powerful than CCA. In most scenarios, AWRR is more powerful than Single-TOW and WSRR.
引用
收藏
页码:162 / 171
页数:10
相关论文
共 50 条
  • [1] Joint Analysis of Multiple Traits Using "Optimal" Maximum Heritability Test
    Wang, Zhenchuan
    Sha, Qiuying
    Zhang, Shuanglin
    PLOS ONE, 2016, 11 (03):
  • [2] Association analysis of multiple traits by an approach of combining P values
    Chen, Lili
    Wang, Yong
    Zhou, Yajing
    JOURNAL OF GENETICS, 2018, 97 (01) : 79 - 85
  • [3] Power Comparisons of Methods for Joint Association Analysis of Multiple Phenotypes
    Zhu, Huanhuan
    Zhang, Shuanglin
    Sha, Qiuying
    HUMAN HEREDITY, 2015, 80 (03) : 144 - 152
  • [4] A Nonparametric Regression Approach to Control for Population Stratification in Rare Variant Association Studies
    Sha, Qiuying
    Zhang, Kui
    Zhang, Shuanglin
    SCIENTIFIC REPORTS, 2016, 6
  • [5] Joint Analysis of Multiple Phenotypes in Association Studies based on Cross-Validation Prediction Error
    Yang, Xinlan
    Zhang, Shuanglin
    Sha, Qiuying
    SCIENTIFIC REPORTS, 2019, 9 (1)
  • [6] Rare variant association test with multiple phenotypes
    Lee, Selyeong
    Won, Sungho
    Kim, Young Jin
    Kim, Yongkang
    Kim, Bong-Jo
    Park, Taesung
    GENETIC EPIDEMIOLOGY, 2017, 41 (03) : 198 - 209
  • [7] Rare-variant genome-wide association studies: a new frontier in genetic analysis of complex traits
    Wagner, Michael J.
    PHARMACOGENOMICS, 2013, 14 (04) : 413 - 424
  • [8] Association analysis of rare and common variants with multiple traits based on variable reduction method
    Chen, Lili
    Wang, Yong
    Zhou, Yajing
    GENETICS RESEARCH, 2018, 100
  • [9] Controlling for human population stratification in rare variant association studies
    Bouaziz, Matthieu
    Mullaert, Jimmy
    Bigio, Benedetta
    Seeleuthner, Yoann
    Casanova, Jean-Laurent
    Alcai, Alexandre
    Abel, Laurent
    Cobat, Aurelie
    SCIENTIFIC REPORTS, 2021, 11 (01)
  • [10] Genetic Association With Multiple Traits in the Presence of Population Stratification
    Yan, Ting
    Li, Qizhai
    Li, Yuanzhang
    Li, Zhaohai
    Zheng, Gang
    GENETIC EPIDEMIOLOGY, 2013, 37 (06) : 571 - 580