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Figure 2 | Journal of Biomedical Science

Figure 2

From: Identifying rare and common disease associated variants in genomic data using Parkinson's disease as a model

Figure 2

Power for detecting the disease gene (280 SNPs) for 5000 cases and 5000 controls. A. 50 rare causal variants (MAF < 1%) in a 1 MB (5086 non-causal SNPs) region of TGP sequencing data with relative risk (rr) of 1.5, 1.7 and 2. B. 70 rare causal variants (MAF < 1%) in a 1 MB (5086 non-causal SNPs) region of TGP sequencing data with rr of 1.5, 1.7 and 2. C. 50 rare causal variants in a 0.1 MB (524 non-causal SNPs) region of TGP sequencing data with rr of 1.5, 1.7 and 2. D. 70 rare causal variants in a 0.1 MB (524 non-causal SNPs) region of TGP sequencing data with rr of 1.5, 1.7 and 2.

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