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The Characterization of Twenty Sequenced Human Genomes

Figure 1

Average per-genome overlap between SNVs in genomic databases and SNVs identified by whole-genome sequencing.

On average, 3,473,639 SNVs were observed in each genome (Table S2). A per-genome average of 87.28% of these SNVs were present in the dbSNP database (version 129, validated) (Table S3).

Figure 1

doi: https://doi.org/10.1371/journal.pgen.1001111.g001