The graphical scenario is presented for M = 10, 000 SNPs; K = 25 annotations; % of annotated SNPs in A1-A6 (u) = 10%; % of overlap between A1-A2, A3-A4, A5-A6 (v) = 50%; A7–A15 are noise SNPs, approximately 20% of which are randomly annotated; blue SNPs are non-null for trait P1 and their GWAS p-values are generated from Beta(α1 = 0.4, 1) distribution; orange SNPs are non-null for trait P2 and their GWAS p-values are generated from Beta(α2 = 0.4, 1) distribution; all other SNPs are null for both traits and their GWAS p-values are generated from U[0, 1] distribution for both traits.</p
Disease models for the two pairs of SNPs that contribute to the simulated outcome. Numeric values (e...
<p>Results for rare variants are shown in red; for the top hit among common variants, results are sh...
<p>Data were simulated based on real data by random selection of 1, 5 or 10 genotyped SNPs at either...
<p>(A) 20% associated SNPs for each phenotype and 75% extra overlaps between and and between and ...
<p>(A) QQ plot of -log10 p values from SNP set tests using different SNP weights under the null simu...
<p>The true positive rate (TPR, row 1), false discovery rate (FDR, row 2) and false positive rate (F...
<p>(A) Histogram of randomly-selected SNPs and highly-selected SNPs, both generated under a null mod...
Quantitative traits are simulated to have broad-sense heritability of H2 = 0.2 with only contributio...
Comparison of (A) AUC, (B) statistical power to detect true marginal and joint risk-associated SNPs ...
Quantitative traits are simulated to have broad-sense heritability of H2 = 0.2 with only contributio...
<p>(A) Extraction of 90 SNPs within 889 model TFBSs of four gap genes from 213 polymorphic individua...
In this work, we define PVE as the total proportion of phenotypic variance that is explained by spar...
<p>Regions of 100 SNPs were simulated from phased 1000 Genomes data in 5,000 individuals, excluding ...
2000 simulated phenotypes for each species and the corresponding causal SNPs information
<p>(a) From our simulated case-control studies, we randomly-sampled markers in order to mimic the as...
Disease models for the two pairs of SNPs that contribute to the simulated outcome. Numeric values (e...
<p>Results for rare variants are shown in red; for the top hit among common variants, results are sh...
<p>Data were simulated based on real data by random selection of 1, 5 or 10 genotyped SNPs at either...
<p>(A) 20% associated SNPs for each phenotype and 75% extra overlaps between and and between and ...
<p>(A) QQ plot of -log10 p values from SNP set tests using different SNP weights under the null simu...
<p>The true positive rate (TPR, row 1), false discovery rate (FDR, row 2) and false positive rate (F...
<p>(A) Histogram of randomly-selected SNPs and highly-selected SNPs, both generated under a null mod...
Quantitative traits are simulated to have broad-sense heritability of H2 = 0.2 with only contributio...
Comparison of (A) AUC, (B) statistical power to detect true marginal and joint risk-associated SNPs ...
Quantitative traits are simulated to have broad-sense heritability of H2 = 0.2 with only contributio...
<p>(A) Extraction of 90 SNPs within 889 model TFBSs of four gap genes from 213 polymorphic individua...
In this work, we define PVE as the total proportion of phenotypic variance that is explained by spar...
<p>Regions of 100 SNPs were simulated from phased 1000 Genomes data in 5,000 individuals, excluding ...
2000 simulated phenotypes for each species and the corresponding causal SNPs information
<p>(a) From our simulated case-control studies, we randomly-sampled markers in order to mimic the as...
Disease models for the two pairs of SNPs that contribute to the simulated outcome. Numeric values (e...
<p>Results for rare variants are shown in red; for the top hit among common variants, results are sh...
<p>Data were simulated based on real data by random selection of 1, 5 or 10 genotyped SNPs at either...