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Chunk #32 — Introduction — Sample sizes and power for GWAS

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The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data.
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large number of effectively independent LD regions in the genome (regions of linkage disequilibrium, with correlated SNPs) and the number of detectable causal loci per phenotype (which is typically small). The first series of studies identifying genetic markers for MRI phenotypes that replicated across independent samples, used a Norwegian discovery sample and replicated the findings in the ADNI or PING cohorts (Joyner et al. 2009; Rimol et al. 2010; Bakken et al. 2012).