Joint Analysis of Multiple Traits Using "Optimal" Maximum Heritability Test

被引:21
|
作者
Wang, Zhenchuan [1 ]
Sha, Qiuying [1 ]
Zhang, Shuanglin [1 ]
机构
[1] Michigan Technol Univ, Dept Math Sci, Houghton, MI 49931 USA
来源
PLOS ONE | 2016年 / 11卷 / 03期
关键词
RARE VARIANTS; PRINCIPAL-COMPONENTS; GENETIC ASSOCIATION; CORRELATED PHENOTYPES; DETECTING ASSOCIATION; QUANTITATIVE TRAITS; SEMIPARAMETRIC TEST; COMMON DISEASES; GENOMIC CONTROL; MODEL APPROACH;
D O I
10.1371/journal.pone.0150975
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
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, most of existing methods use all of the traits for testing the association between multiple traits and a single variant. However, those methods for association studies may lose power in the presence of a large number of noise traits. In this paper, we propose an "optimal" maximum heritability test (MHT-O) to test the association between multiple traits and a single variant. MHT-O includes a procedure of deleting traits that have weak or no association with the variant. Using extensive simulation studies, we compare the performance of MHT-O with MHT, Trait-based Association Test uses Extended Simes procedure (TATES), SUM_SCORE and MANOVA. Our results show that, in all of the simulation scenarios, MHT-O is either the most powerful test or comparable to the most powerful test among the five tests we compared.
引用
收藏
页数:12
相关论文
共 50 条
  • [21] A powerful association test of multiple genetic variants using a random-effects model
    Cheng, K. F.
    Lee, J. Y.
    Zheng, W.
    Li, C.
    STATISTICS IN MEDICINE, 2014, 33 (11) : 1816 - 1827
  • [22] Power Comparisons of Methods for Joint Association Analysis of Multiple Phenotypes
    Zhu, Huanhuan
    Zhang, Shuanglin
    Sha, Qiuying
    HUMAN HEREDITY, 2015, 80 (03) : 144 - 152
  • [23] MF-TOWmuT: Testing an optimally weighted combination of common and rare variants with multiple traits using family data
    Gao, Cheng
    Sha, Qiuying
    Zhang, Shuanglin
    Zhang, Kui
    GENETIC EPIDEMIOLOGY, 2021, 45 (01) : 64 - 81
  • [24] Joint multiple quantitative trait loci mapping for allometries of body compositions and metabolic traits to body weights in broiler
    Zhou, X.
    Zhang, Y.
    Zhang, H.
    Du, J.
    Ye, J.
    Xu, Y.
    Yang, R.
    ANIMAL, 2020, 14 (06) : 1120 - 1127
  • [25] Estimation and Partition of Heritability in Human Populations Using Whole-Genome Analysis Methods
    Vinkhuyzen, Anna A. E.
    Wray, Naomi R.
    Yang, Jian
    Goddard, Michael E.
    Visscher, Peter M.
    ANNUAL REVIEW OF GENETICS, VOL 47, 2013, 47 : 75 - +
  • [26] Genetic Variance Components Estimation for Binary Traits Using Multiple Related Individuals
    Papachristou, Charalampos
    Ober, Carole
    Abney, Mark
    GENETIC EPIDEMIOLOGY, 2011, 35 (05) : 291 - 302
  • [27] An Empirical Bayes risk prediction model using multiple traits for sequencing data
    Li, Gengxin
    Cui, Yuehua
    Zhao, Hongyu
    STATISTICAL APPLICATIONS IN GENETICS AND MOLECULAR BIOLOGY, 2015, 14 (06) : 551 - 573
  • [28] An Efficient Stepwise Statistical Test to Identify Multiple Linked Human Genetic Variants Associated with Specific Phenotypic Traits
    Huh, Iksoo
    Kwon, Min-Seok
    Park, Taesung
    PLOS ONE, 2015, 10 (09):
  • [29] On a semiparametric test to detect associations between quantitative traits and candidate genes using unrelated individuals
    Zhang, SL
    Zhu, XF
    Zhao, HY
    GENETIC EPIDEMIOLOGY, 2003, 24 (01) : 44 - 56
  • [30] Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease
    Keller, Margaux F.
    Saad, Mohamad
    Bras, Jose
    Bettella, Francesco
    Nicolaou, Nayia
    Simon-Sanchez, Javier
    Mittag, Florian
    Buechel, Finja
    Sharma, Manu
    Gibbs, J. Raphael
    Schulte, Claudia
    Moskvina, Valentina
    Durr, Alexandra
    Holmans, Peter
    Kilarski, Laura L.
    Guerreiro, Rita
    Hernandez, Dena G.
    Brice, Alexis
    Ylikotila, Pauli
    Stefansson, Hreinn
    Majamaa, Kari
    Morris, Huw R.
    Williams, Nigel
    Gasser, Thomas
    Heutink, Peter
    Wood, Nicholas W.
    Hardy, John
    Martinez, Maria
    Singleton, Andrew B.
    Nalls, Michael A.
    HUMAN MOLECULAR GENETICS, 2012, 21 (22) : 4996 - 5009