Low-coverage sequencing: Implications for design of complex trait association studies

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Figure 7.
Figure 7.

Power of association mapping by sequencing depth and number of individuals sequenced. We simulated 1500 cases and 1500 controls, assuming a single causal variant with causal allele frequency 0.5%, 1%, or 3%. We sequenced all 3000 individuals or a random subset of 400, 1000, or 2000 individuals (equal number of cases and controls) at depths ranging from 2×–30×. Power was estimated using an empirical threshold determined from 500 null sets to ensure familywise type-I error of 5%.

This Article

  1. Genome Res. 21: 940-951

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