SNP detection and genotyping from low-coverage sequencing data on multiple diploid samples

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Figure 3.
Figure 3.

SNP discovery power for different sequencing strategies as a function of the non-reference allele frequency in the population. The continuous lines show empirical results from the simulation with the allele frequency estimated from all 3000 simulated haplotypes, and the dashed lines present calculations based on sampling with marginal discovery rates per sample from Figure 2.

This Article

  1. Genome Res. 21: 952-960

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