TY - JOUR T1 - Using imputed genotype data in the joint score tests for genetic association and gene-environment interactions in case-control studies JF - bioRxiv DO - 10.1101/062075 SP - 062075 AU - Minsun Song AU - William Wheeler AU - Neil E. Caporaso AU - Maria Teresa Landi AU - Nilanjan Chatterjee Y1 - 2016/01/01 UR - http://biorxiv.org/content/early/2016/07/04/062075.abstract N2 - Background Genome-wide association studies (GWAS) are now routinely imputed for untyped SNPs based on various powerful statistical algorithms for imputation trained on reference datasets. The use of predicted allele count for imputed SNPs as the dosage variable is known to produce valid score test for genetic association.Methods In this paper, we investigate how to best handle imputed SNPs in various modern complex tests for genetic association incorporating gene-environment interactions. We focus on case-control association studies where inference in an underlying logistic regression model can be performed using alternative methods that rely on varying degree on an assumption of gene-environment independence in the underlying population. As increasingly large scale GWAS are being performed through consortia effort where it is preferable to share only summary-level information across studies, we also describe simple mechanisms for implementing score-tests based on standard meta-analysis of “one-step” maximum-likelihood estimates across studies.Results Applications of the methods in simulation studies and a dataset from genome-wide association study of lung cancer illustrate ability of the proposed methods to maintain type-I error rates for underlying testing procedures. For analysis of imputed SNPs, similar to typed SNPs, retrospective methods can lead to considerable efficiency gain for modeling of gene-environment interactions under the assumption of gene-environment independence.Conclusions Proposed methods allow valid analysis of imputed SNPs in case-control studies of gene-environment interaction using alternative strategies that had been earlier available only for genotyped SNPs. ER -