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. Author manuscript; available in PMC: 2017 Dec 18.
Published in final edited form as: Nat Methods. 2016 Oct 10;13(11):953–958. doi: 10.1038/nmeth.4028

Figure 2.

Figure 2

Characterization of Simul-seq whole-genome data. (a) Coverage distributions for Simul-seq and DNA-seq genomes of the same individual11. (b) Lorenz curves for the cumulative fraction of the covered genome versus the cumulative fraction of total mapped bases. Black line indicates the theoretical limit for independent sampling. (c) Comparison of single-nucleotide variant (SNV) calls between Simul-seq and DNA-seq genomes. (d) Comparison of insertion and deletions (indels) calls and size distributions between Simul-seq and DNA-seq genomes.