Sequential Sentinel SNP Regional Association Plots (SSS‐RAP): An Approach for Testing Independence of SNP Association Signals Using Meta‐Analysis Data

Genome‐Wide Association Studies (GWAS) frequently incorporate meta‐analysis within their framework. However, conditional analysis of individual‐level data, which is an established approach for fine mapping of causal sites, is often precluded where only group‐level summary data are available for analysis. Here, we present a numerical and graphical approach, “sequential sentinel SNP regional association plot” (SSS‐RAP), which estimates regression coefficients (beta) with their standard errors using the meta‐analysis summary results directly. Under an additive model, typical for genes with small effect, the effect for a sentinel SNP can be transformed to the predicted effect for a possibly dependent SNP through a 2×2 2‐SNP haplotypes table. The approach assumes Hardy–Weinberg equilibrium for test SNPs. SSS‐RAP is available as a Web‐tool (http://apps.biocompute.org.uk/sssrap/sssrap.cgi). To develop and illustrate SSS‐RAP we analyzed lipid and ECG traits data from the British Women's Heart and Health Study (BWHHS), evaluated a meta‐analysis for ECG trait and presented several simulations. We compared results with existing approaches such as model selection methods and conditional analysis. Generally findings were consistent. SSS‐RAP represents a tool for testing independence of SNP association signals using meta‐analysis data, and is also a convenient approach based on biological principles for fine mapping in group level summary data.

[1]  John P. A. Ioannidis,et al.  The Emergence of Networks in Human Genome Epidemiology: Challenges and Opportunities , 2007, Epidemiology.

[2]  Santiago Rodríguez,et al.  Cubic exact solutions for the estimation of pairwise haplotype frequencies: implications for linkage disequilibrium analyses and a web tool 'CubeX' , 2007, BMC Bioinformatics.

[3]  Henggui Zhang,et al.  Integration of Genetics into a Systems Model of Electrocardiographic Traits Using HumanCVD BeadChip , 2012, Circulation. Cardiovascular genetics.

[4]  D. Lawlor,et al.  Geographical variation in cardiovascular disease, risk factors, and their control in older women: British Women's Heart and Health Study , 2003, Journal of epidemiology and community health.

[5]  Paolo Vineis,et al.  A road map for efficient and reliable human genome epidemiology , 2006, Nature Genetics.

[6]  P. Donnelly,et al.  A Flexible and Accurate Genotype Imputation Method for the Next Generation of Genome-Wide Association Studies , 2009, PLoS genetics.

[7]  Tom R. Gaunt,et al.  Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip. , 2009, American journal of human genetics.

[8]  Sharon R Grossman,et al.  Integrating common and rare genetic variation in diverse human populations , 2010, Nature.

[9]  M. McCarthy,et al.  An evaluation of HapMap sample size and tagging SNP performance in large-scale empirical and simulated data sets , 2005, Nature Genetics.

[10]  R. Lewontin The Interaction of Selection and Linkage. I. General Considerations; Heterotic Models. , 1964, Genetics.

[11]  P. McKeigue,et al.  Problems of reporting genetic associations with complex outcomes , 2003, The Lancet.

[12]  Anne Cambon-Thomsen,et al.  Assessing the impact of biobanks , 2003, Nature Genetics.

[13]  W. G. Hill,et al.  Linkage disequilibrium in finite populations , 1968, Theoretical and Applied Genetics.

[14]  Dolores Corella,et al.  Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans , 2008, Nature Genetics.

[15]  Tom R. Gaunt,et al.  Analysis of Potential Genomic Confounding in Genetic Association Studies and an Online Genomic Confounding Browser (GCB) , 2011, Annals of human genetics.

[16]  L. Cardon,et al.  Association study designs for complex diseases , 2001, Nature Reviews Genetics.

[17]  D. Altshuler,et al.  A map of human genome variation from population-scale sequencing , 2010, Nature.

[18]  Fotios Drenos,et al.  Application of statistical and functional methodologies for the investigation of genetic determinants of coronary heart disease biomarkers: lipoprotein lipase genotype and plasma triglycerides as an exemplar , 2010, Human molecular genetics.

[19]  Manuel A. R. Ferreira,et al.  PLINK: a tool set for whole-genome association and population-based linkage analyses. , 2007, American journal of human genetics.