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

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Figure 4.
Figure 4.

Marginal discovery rates as a function of non-reference allele count in 43 samples, from the CEU simulation and from 1000 Genomes Project data evaluated at HapMap 2 sites not in HapMap 3, on the 43 sequenced samples overlapping HapMap 2.

This Article

  1. Genome Res. 21: 952-960

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