Bias-reduced estimators and confidence intervals for odds ratios in genome-wide association studies.

Genome-wide association studies (GWAS) provide an important approach to identifying common genetic variants that predispose to human disease. A typical GWAS may genotype hundreds of thousands of single nucleotide polymorphisms (SNPs) located throughout the human genome in a set of cases and controls. Logistic regression is often used to test for association between a SNP genotype and case versus control status, with corresponding odds ratios (ORs) typically reported only for those SNPs meeting selection criteria. However, when these estimates are based on the original data used to detect the variant, the results are affected by a selection bias sometimes referred to the "winner's curse" (Capen and others, 1971). The actual genetic association is typically overestimated. We show that such selection bias may be severe in the sense that the conditional expectation of the standard OR estimator may be quite far away from the underlying parameter. Also standard confidence intervals (CIs) may have far from the desired coverage rate for the selected ORs. We propose and evaluate 3 bias-reduced estimators, and also corresponding weighted estimators that combine corrected and uncorrected estimators, to reduce selection bias. Their corresponding CIs are also proposed. We study the performance of these estimators using simulated data sets and show that they reduce the bias and give CI coverage close to the desired level under various scenarios, even for associations having only small statistical power.

[1]  F. Galton Regression Towards Mediocrity in Hereditary Stature. , 1886 .

[2]  W. G. Cochran Some Methods for Strengthening the Common χ 2 Tests , 1954 .

[3]  P. Armitage Tests for Linear Trends in Proportions and Frequencies , 1955 .

[4]  E. C. Capen,et al.  Competitive Bidding in High-Risk Situations , 1971 .

[5]  R. Tsay Nonlinearity tests for time series , 1986 .

[6]  John Whitehead,et al.  On the bias of maximum likelihood estimation following a sequential test , 1986 .

[7]  Alan Agresti,et al.  Categorical Data Analysis , 1991, International Encyclopedia of Statistical Science.

[8]  Y. Benjamini,et al.  Controlling the false discovery rate: a practical and powerful approach to multiple testing , 1995 .

[9]  N Risch,et al.  The Future of Genetic Studies of Complex Human Diseases , 1996, Science.

[10]  D Siegmund,et al.  Upward bias in estimation of genetic effects. , 2002, American journal of human genetics.

[11]  Lei Sun,et al.  Reduction of selection bias in genomewide studies by resampling , 2005, Genetic epidemiology.

[12]  Shelley B. Bull,et al.  Locus-Specific Heritability Estimation via the Bootstrap in Linkage Scans for Quantitative Trait Loci , 2006, Human Heredity.

[13]  G. Abecasis,et al.  Joint analysis is more efficient than replication-based analysis for two-stage genome-wide association studies , 2006, Nature Genetics.

[14]  Lihong Qi,et al.  Aspects of the design and analysis of high-dimensional SNP studies for disease risk estimation. , 2006, Biostatistics.

[15]  Chad Garner,et al.  Upward bias in odds ratio estimates from genome‐wide association studies , 2007, Genetic epidemiology.

[16]  Qizhai Li,et al.  Flexible design for following up positive findings. , 2007, American journal of human genetics.

[17]  W. Willett,et al.  A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer , 2007, Nature Genetics.

[18]  C. Gieger,et al.  Genomewide association analysis of coronary artery disease. , 2007, The New England journal of medicine.

[19]  Lester L. Peters,et al.  Genome-wide association study identifies novel breast cancer susceptibility loci , 2007, Nature.

[20]  J. Pritchard,et al.  Overcoming the winner's curse: estimating penetrance parameters from case-control data. , 2007, American journal of human genetics.

[21]  Simon C. Potter,et al.  Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls , 2007, Nature.