Literature DB >> 19397584

Improving power for testing genetic association in case-control studies by reducing the alternative space.

Jungnam Joo1, Minjung Kwak, Gang Zheng.   

Abstract

To detect association between a genetic marker and a disease in case-control studies, the Cochran-Armitage trend test is typically used. The trend test is locally optimal when the genetic model is correctly specified. However, in practice, the underlying genetic model, and hence the optimal trend test, are usually unknown. In this case, Pearson's chi-squared test, the maximum of three trend test statistics (optimal for the recessive, additive, and dominant models), and the test based on genetic model selection (GMS) are useful. In this article, we first modify the existing GMS method so that it can be used when the risk allele is unknown. Then we propose a new approach by excluding a genetic model that is not supported by the data. Using either the model selection or exclusion, the alternative space is reduced conditional on the observed data, and hence the power to detect a true association can be increased. Simulation results are reported and the proposed methods are applied to the genetic markers identified from the genome-wide association studies conducted by the Wellcome Trust Case-Control Consortium. The results demonstrate that the genetic model exclusion approach usually performs better than existing methods under its worst situation across scientifically plausible genetic models we considered.

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Year:  2009        PMID: 19397584     DOI: 10.1111/j.1541-0420.2009.01241.x

Source DB:  PubMed          Journal:  Biometrics        ISSN: 0006-341X            Impact factor:   2.571


  11 in total

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2.  Incorporating parental information into family-based association tests.

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3.  A new system identification approach to identify genetic variants in sequencing studies for a binary phenotype.

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Journal:  Hum Hered       Date:  2014-07-30       Impact factor: 0.444

4.  Robust tests for matched case-control genetic association studies.

Authors:  Yong Zang; Wing Kam Fung
Journal:  BMC Genet       Date:  2010-10-12       Impact factor: 2.797

5.  Emerging molecular technologies for identifying the risk of second cancers.

Authors:  Susan T Mayne; Stephen B Gruber
Journal:  Cancer Prev Res (Phila)       Date:  2009-07

6.  Case-Control Genome-wide Joint Association Study Using Semiparametric Empirical Model and Approximate Bayes Factor.

Authors:  Jinfeng Xu; Gang Zheng; Ao Yuan
Journal:  J Stat Comput Simul       Date:  2013-01-01       Impact factor: 1.424

7.  A rapid association test procedure robust under different genetic models accounting for population stratification.

Authors:  Wenan Chen; Xiangning Chen; Kellie J Archer; Nianjun Liu; Qizhai Li; Zhongming Zhao; Shumei Sun; Guimin Gao
Journal:  Hum Hered       Date:  2013-04-03       Impact factor: 0.444

8.  A Pragmatic Test for Detecting Association between a Dichotomous Trait and the Genotypes of Affected Families, Controls and Independent Cases.

Authors:  Meng Wang; William C L Stewart
Journal:  Front Genet       Date:  2017-05-09       Impact factor: 4.599

9.  Robust Association Tests for the Replication of Genome-Wide Association Studies.

Authors:  Jungnam Joo; Ju-Hyun Park; Bora Lee; Boram Park; Sohee Kim; Kyong-Ah Yoon; Jin Soo Lee; Nancy L Geller
Journal:  Biomed Res Int       Date:  2015-08-04       Impact factor: 3.411

10.  A new association test based on disease allele selection for case-control genome-wide association studies.

Authors:  Zhongxue Chen
Journal:  BMC Genomics       Date:  2014-05-12       Impact factor: 3.969

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