Joint Analysis of Multiple Traits Using "Optimal" Maximum Heritability Test
被引:21
|
作者:
Wang, Zhenchuan
论文数: 0引用数: 0
h-index: 0
机构:
Michigan Technol Univ, Dept Math Sci, Houghton, MI 49931 USAMichigan Technol Univ, Dept Math Sci, Houghton, MI 49931 USA
Wang, Zhenchuan
[1
]
Sha, Qiuying
论文数: 0引用数: 0
h-index: 0
机构:
Michigan Technol Univ, Dept Math Sci, Houghton, MI 49931 USAMichigan Technol Univ, Dept Math Sci, Houghton, MI 49931 USA
Sha, Qiuying
[1
]
Zhang, Shuanglin
论文数: 0引用数: 0
h-index: 0
机构:
Michigan Technol Univ, Dept Math Sci, Houghton, MI 49931 USAMichigan Technol Univ, Dept Math Sci, Houghton, MI 49931 USA
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.
机构:
Univ Sci, Dept Math Phys & Stat, Philadelphia, PA 19104 USA
Univ Chicago, Dept Human Genet, Chicago, IL 60637 USAUniv Sci, Dept Math Phys & Stat, Philadelphia, PA 19104 USA
Papachristou, Charalampos
Ober, Carole
论文数: 0引用数: 0
h-index: 0
机构:
Univ Chicago, Dept Human Genet, Chicago, IL 60637 USAUniv Sci, Dept Math Phys & Stat, Philadelphia, PA 19104 USA
Ober, Carole
Abney, Mark
论文数: 0引用数: 0
h-index: 0
机构:
Univ Chicago, Dept Human Genet, Chicago, IL 60637 USAUniv Sci, Dept Math Phys & Stat, Philadelphia, PA 19104 USA
机构:
Seoul Natl Univ, Dept Stat, Seoul, South KoreaSeoul Natl Univ, Dept Stat, Seoul, South Korea
Huh, Iksoo
Kwon, Min-Seok
论文数: 0引用数: 0
h-index: 0
机构:
Seoul Natl Univ, Interdisciplinary Program Bioinformat, Seoul, South KoreaSeoul Natl Univ, Dept Stat, Seoul, South Korea
Kwon, Min-Seok
Park, Taesung
论文数: 0引用数: 0
h-index: 0
机构:
Seoul Natl Univ, Dept Stat, Seoul, South Korea
Seoul Natl Univ, Interdisciplinary Program Bioinformat, Seoul, South KoreaSeoul Natl Univ, Dept Stat, Seoul, South Korea
机构:
Cardiff Univ, MRC, Ctr Neuropsychiat Genet & Genom, Sch Med, Cardiff, S Glam, Wales
Cardiff Univ, Inst Psychol Med & Clin Neurosci, Cardiff, S Glam, WalesNIA, Mol Genet Sect, Neurogenet Lab, NIH, Bethesda, MD 20892 USA
Moskvina, Valentina
Durr, Alexandra
论文数: 0引用数: 0
h-index: 0
机构:
Univ Paris 06, Ctr Rech, Inst Cerveau & Moelle Epiniere, UMR S975, Paris, France
Hop La Pitie Salpetriere, AP HP, Dept Genet, Paris, France
INSERM, UMR S975, Paris, France
CNRS, UMR 7225, Paris, FranceNIA, Mol Genet Sect, Neurogenet Lab, NIH, Bethesda, MD 20892 USA
Durr, Alexandra
Holmans, Peter
论文数: 0引用数: 0
h-index: 0
机构:
Cardiff Univ, MRC, Ctr Neuropsychiat Genet & Genom, Sch Med, Cardiff, S Glam, Wales
Cardiff Univ, Inst Psychol Med & Clin Neurosci, Cardiff, S Glam, WalesNIA, Mol Genet Sect, Neurogenet Lab, NIH, Bethesda, MD 20892 USA
Holmans, Peter
Kilarski, Laura L.
论文数: 0引用数: 0
h-index: 0
机构:
Cardiff Univ, MRC, Ctr Neuropsychiat Genet & Genom, Sch Med, Cardiff, S Glam, Wales
Cardiff Univ, Inst Psychol Med & Clin Neurosci, Cardiff, S Glam, WalesNIA, Mol Genet Sect, Neurogenet Lab, NIH, Bethesda, MD 20892 USA
机构:
Univ Paris 06, Ctr Rech, Inst Cerveau & Moelle Epiniere, UMR S975, Paris, France
Hop La Pitie Salpetriere, AP HP, Dept Genet, Paris, France
INSERM, UMR S975, Paris, France
CNRS, UMR 7225, Paris, FranceNIA, Mol Genet Sect, Neurogenet Lab, NIH, Bethesda, MD 20892 USA
Brice, Alexis
Ylikotila, Pauli
论文数: 0引用数: 0
h-index: 0
机构:
Turku Univ Hosp, Dept Neurol, Turku, Finland
Univ Turku, SF-20500 Turku, FinlandNIA, Mol Genet Sect, Neurogenet Lab, NIH, Bethesda, MD 20892 USA