<p>(A) Histogram of randomly-selected SNPs and highly-selected SNPs, both generated under a null model and uncorrected for multiple testing. The selected SNPs were obtained by taking the most significant SNP from a set of 1,400 null SNPs. The random SNPs were obtained by randomly-selecting a marker from the 198k SNPs. The 200 presented data points were generated from 200 iterations of the simulation. (B) Distribution of −log(<i>P</i>-value) for global likelihood ratio test from the observed method and the permuted method that mimic Lesnick's model selection scheme (see <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0002707#s4" target="_blank">Materials and Methods</a>). <i>P</i>-values were tallied from 500 observed m...
<p>(A) Recovery of global features of simulated ARGs from sequence data. This plot is based on sets ...
<p>Simulation Results: Parameter estimates resulting from simulation for the model with and without ...
<p>In scenario I, only phenotype 1 is associated with the SNP. <i>rG</i> = 1 or −1 does not affect t...
The graphical scenario is presented for M = 10, 000 SNPs; K = 25 annotations; % of annotated SNPs in...
<p>(A) 20% associated SNPs for each phenotype and 75% extra overlaps between and and between and ...
<p>Simulation study 2: Mean number of pathways and SNPs selected by each model at each effect size, ...
<p>The figure plots the mean (A) genotype error and (B) clone frequency error as a function of the...
<p>OR is tabulated for each genotype of causal SNPs as in Namkung <i>et al.</i><a href="http://www.p...
<p>(A) QQ plot of -log10 p values from SNP set tests using different SNP weights under the null simu...
<p>The first to third columns denote the effect sizes of SNP1, SNP2 and interaction in pure samples ...
<p>The true positive rate (TPR, row 1), false discovery rate (FDR, row 2) and false positive rate (F...
<p>144 genes are selected from the Broad data set. Each gene has exactly rare variants, . For each ...
<p>(A) Extraction of 90 SNPs within 889 model TFBSs of four gap genes from 213 polymorphic individua...
<p>Before carrying out these steps, a large pool of haplotypes (<i>n</i> = 15,000) was simulated. Gi...
<p>Shown here are representative examples of simulation results for available software including the...
<p>(A) Recovery of global features of simulated ARGs from sequence data. This plot is based on sets ...
<p>Simulation Results: Parameter estimates resulting from simulation for the model with and without ...
<p>In scenario I, only phenotype 1 is associated with the SNP. <i>rG</i> = 1 or −1 does not affect t...
The graphical scenario is presented for M = 10, 000 SNPs; K = 25 annotations; % of annotated SNPs in...
<p>(A) 20% associated SNPs for each phenotype and 75% extra overlaps between and and between and ...
<p>Simulation study 2: Mean number of pathways and SNPs selected by each model at each effect size, ...
<p>The figure plots the mean (A) genotype error and (B) clone frequency error as a function of the...
<p>OR is tabulated for each genotype of causal SNPs as in Namkung <i>et al.</i><a href="http://www.p...
<p>(A) QQ plot of -log10 p values from SNP set tests using different SNP weights under the null simu...
<p>The first to third columns denote the effect sizes of SNP1, SNP2 and interaction in pure samples ...
<p>The true positive rate (TPR, row 1), false discovery rate (FDR, row 2) and false positive rate (F...
<p>144 genes are selected from the Broad data set. Each gene has exactly rare variants, . For each ...
<p>(A) Extraction of 90 SNPs within 889 model TFBSs of four gap genes from 213 polymorphic individua...
<p>Before carrying out these steps, a large pool of haplotypes (<i>n</i> = 15,000) was simulated. Gi...
<p>Shown here are representative examples of simulation results for available software including the...
<p>(A) Recovery of global features of simulated ARGs from sequence data. This plot is based on sets ...
<p>Simulation Results: Parameter estimates resulting from simulation for the model with and without ...
<p>In scenario I, only phenotype 1 is associated with the SNP. <i>rG</i> = 1 or −1 does not affect t...