Figure 6
From: Methods for detecting associations between phenotype and aggregations of rare variants
MCMC results for analysis of quantitative trait Q2. Histogram showing the frequency with which each SNP was included in the subset of SNPs on which the optimal score statistic was calculated, aggregated across all 200 replicates. Results are for chromosome 6 (top), chromosome 17 (middle), and chromosome 21 (bottom). The x-axis indexes the SNPs on the given chromosome (each bar corresponds to a single SNP; bars are equally spaced for clarity). The y-axis shows the frequency with which the SNP was included in the optimal solution. Red x’s indicate positions of SNPs that are associated with the trait (according to GAW17 answers).