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. 2019 Mar 5;8:e40538. doi: 10.7554/eLife.40538

Table 1. Power to detect simulated correlation QTL across a wide range of scenarios (n = 1000 for all simulations).

Simulation parameters
(1) Correlation QTL effect* x x x x x x x x
(2) Genotype predicts the mean of gene one expression levels (e.g., through an eQTL or proportion QTL) x x x
(3) Genotype predicts the mean of gene two expression levels x
(4) Genotype predicts the variance of gene one expression levels (e.g., through a varQTL) x x
(5) A variable that is random with respect to genotype predicts the mean of gene one expression levels(e.g., through technical, environmental, or cell type heterogeneity effects) x
(6) A variable that is random with respect to genotype predicts the mean of gene two expression levels x
(7) A variable that is random with respect to genotype predicts the variance of gene one expression levels(e.g., through technical, environmental, or cell type heterogeneity effects) x x
(8) A variable that is random with respect to genotype predicts the variance of gene two expression levels x
Results
Power (proportion of true positives detected, Bonferroni-corrected p<0.05) 0.5091 0.4934 0.5055 0.0716 0.0679 0.4998 0.0884 0.0533
False positive rate (proportion of true negatives detected, nominal p<0.05) 0.0519 0.0529 0.0494 0.0532 0.0507 0.0527 0.0529 0.0522

Simulated effect sizes were as follows: correlation QTL* = 0.3, mean effects = 1, variance effects  = 10. When Bonferroni-corrected p-values were used, the false positive rate was 0 across all simulation scenarios. Abbreviations: eQTL = expression QTL and vQTL = variance QTL.