On the choice of degrees of freedom for testing gene-gene interactions

被引:6
|
作者
Ueki, Masao [1 ]
机构
[1] Tohoku Univ, Grad Sch Med, Tohoku Med Megabank Org, Aoba Ku, Sendai, Miyagi 9808573, Japan
关键词
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.
引用
收藏
页码:4934 / 4948
页数:15
相关论文
共 50 条
  • [31] Testing Gene-Gene Interactions Based on a Neighborhood Perspective in Genome-wide Association Studies
    Guo, Yingjie
    Cheng, Honghong
    Yuan, Zhian
    Liang, Zhen
    Wang, Yang
    Du, Debing
    FRONTIERS IN GENETICS, 2021, 12
  • [32] FASTCHI: AN EFFICIENT ALGORITHM FOR ANALYZING GENE-GENE INTERACTIONS
    Zhang, Xiang
    Zou, Fei
    Wang, Wei
    PACIFIC SYMPOSIUM ON BIOCOMPUTING 2009, 2009, : 528 - +
  • [33] Pharmacogenomics of Hypertension and Preeclampsia: Focus on Gene-Gene Interactions
    Luizon, Marcelo R.
    Pereira, Daniela A.
    Sandrim, Valeria C.
    FRONTIERS IN PHARMACOLOGY, 2018, 9
  • [34] Neighborhood-based clustering of gene-gene interactions
    Diaz-Diaz, Norberto
    Rodriguez-Baena, Domingo S.
    Nepomuceno, Isabel
    Aguilar-Ruiz, Jesus S.
    INTELLIGENT DATA ENGINEERING AND AUTOMATED LEARNING - IDEAL 2006, PROCEEDINGS, 2006, 4224 : 1111 - 1120
  • [35] Pathway-Guided Identification of Gene-Gene Interactions
    Wang, Xin
    Zhang, Daowen
    Tzeng, Jung-Ying
    ANNALS OF HUMAN GENETICS, 2014, 78 (06) : 478 - 491
  • [36] Investigating the Role of Gene-Gene Interactions in TB Susceptibility
    Daya, Michelle
    van der Merwe, Lize
    van Helden, Paul D.
    Moeller, Marlo
    Hoal, Eileen G.
    PLOS ONE, 2015, 10 (04):
  • [37] Identification of multiple gene-gene interactions for ordinal phenotypes
    Kyunga Kim
    Min-Seok Kwon
    Sohee Oh
    Taesung Park
    BMC Medical Genomics, 6
  • [38] Detecting gene-gene interactions: MDR versus CART
    不详
    GENETIC EPIDEMIOLOGY, 2004, 27 (03) : 263 - 264
  • [39] Gene-gene Interactions in Paget's Disease of Bone
    Guay-Belanger, Sabrina
    Simonyan, David
    Gagnon, Edith
    Morissette, Jean
    Brown, Jacques P.
    Michou, Laetitia
    JOURNAL OF BONE AND MINERAL RESEARCH, 2014, 29 : S129 - S129
  • [40] Identification of multiple gene-gene interactions for ordinal phenotypes
    Kim, Kyunga
    Kwon, Min-Seok
    Oh, Sohee
    Park, Taesung
    BMC MEDICAL GENOMICS, 2013, 6