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Figure 1 | BMC Proceedings

Figure 1

From: Detecting disease rare alleles using single SNPs in families and haplotyping in unrelated subjects from the Genetic Analysis Workshop 17 data

Figure 1

Genome-wide linear mixed effects additive model association test results of 200 replications of family-based cohort data on Q2 residuals. None of the SNPs’ −log10p mean values passed the 5.4 genome-wide threshold. Sens. = sensitivity. Red triangles mark chromosomes that were simulated with Q2 causative SNPs (72 of them in 13 genes).

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BMC Proceedings

ISSN: 1753-6561

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