On the choice of degrees of freedom for testing gene-gene interactions
被引:6
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作者:
Ueki, Masao
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机构:
Tohoku Univ, Grad Sch Med, Tohoku Med Megabank Org, Aoba Ku, Sendai, Miyagi 9808573, JapanTohoku Univ, Grad Sch Med, Tohoku Med Megabank Org, Aoba Ku, Sendai, Miyagi 9808573, Japan
Ueki, Masao
[1
]
机构:
[1] Tohoku Univ, Grad Sch Med, Tohoku Med Megabank Org, Aoba Ku, Sendai, Miyagi 9808573, Japan
decomposition of type I error;
degrees of freedom;
gene-gene interaction;
prospective sampling;
retrospective sampling;
MULTIFACTOR-DIMENSIONALITY REDUCTION;
ASSOCIATION;
SELECTION;
TOOL;
D O I:
10.1002/sim.6264
中图分类号:
Q [生物科学];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
In gene-gene interaction analysis using single nucleotide polymorphism (SNP) data, empty cells arise in the genotype contingency table more frequently than in single SNP association studies. Empty cells lead to unidentifiable regression coefficients in regression model fitting. It is unclear whether the degrees of freedom (d.f.) for testing interactions are reduced for such sparse contingency tables. BooleanOperation based Screening and Testing is an exhaustive gene-gene interaction search method in which a fixed d.f. of four (the most conservative choice) is used in the chi-squared null distribution for the likelihood ratio test for gene-gene interactions under a logistic regression model. In this paper, the choice of d. f. is investigated theoretically by introducing a decomposition of type I error. An adaptive method using the observed d. f. can be less conservative than the fixed d. f. method, thereby enhancing power. In simulated data, type I error rates for the adaptive method were usually better controlled under various scenarios for Gaussian linear regression and logistic regression, including prospective and retrospective sampling designs, as well as for artificial data that mimic actual genome-wide SNPs. When the adaptive method was applied to public datasets generated from simulations, it exhibited an improvement in power over the fixed method. Copyright (C) 2014 John Wiley & Sons, Ltd.
机构:
Univ Washington, Dept Biostat, Seattle, WA 98195 USAUniv Washington, Dept Biostat, Seattle, WA 98195 USA
Hu, Jie Kate
Wang, Xianlong
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机构:
Fred Hutchinson Canc Res Ctr, Seattle, WA 98109 USAUniv Washington, Dept Biostat, Seattle, WA 98195 USA
Wang, Xianlong
Wang, Pei
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机构:
Fred Hutchinson Canc Res Ctr, Seattle, WA 98109 USA
Icahn Sch Med Mt Sinai, Icahn Inst Genom & Multiscale Biol, New York, NY USAUniv Washington, Dept Biostat, Seattle, WA 98195 USA
机构:
Harbor UCLA Med Ctr, Los Angeles Biomed Res Inst, Torrance, CA 90509 USA
Harbor UCLA Med Ctr, Dept Psychiat, Torrance, CA 90509 USAVita Genom Inc, Taipei, Taiwan
Tsai, Guochuan E.
Lin, Eugene
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机构:
Vita Genom Inc, Taipei, Taiwan
China Med Univ, Inst Clin Med Sci, Taichung, TaiwanVita Genom Inc, Taipei, Taiwan
机构:
Mem Univ Newfoundland, Fac Med, Disciplines Lab Med Genet & Pediat, St Johns, NF A1B 3V6, CanadaMem Univ Newfoundland, Fac Med, Disciplines Lab Med Genet & Pediat, St Johns, NF A1B 3V6, Canada
Xie, YG
Butt, C
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Mem Univ Newfoundland, Fac Med, Disciplines Lab Med Genet & Pediat, St Johns, NF A1B 3V6, CanadaMem Univ Newfoundland, Fac Med, Disciplines Lab Med Genet & Pediat, St Johns, NF A1B 3V6, Canada
Butt, C
Randell, E
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机构:
Mem Univ Newfoundland, Fac Med, Disciplines Lab Med Genet & Pediat, St Johns, NF A1B 3V6, CanadaMem Univ Newfoundland, Fac Med, Disciplines Lab Med Genet & Pediat, St Johns, NF A1B 3V6, Canada