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. 2018 Oct 29;35(11):1901–1906. doi: 10.1093/bioinformatics/bty898

Fig. 1.

Fig. 1.

Results from simGWAS (sG) are visually similar to those from HAPGEN+SNPTEST (HG). The figure shows ∼350 SNPs from around the causal variants in the simulated region under scenario 4, with 5000 cases and 5000 controls. Points show the median −log10(P value) for each SNP, and ranges the IQR across 1000 simulations. Location of causal variants are marked with dotted lines