Figure 3.
Relationship between distribution of different types of sequence variants. Density of sequence variants was calculated in 1-Mb windows of the BN reference genome, normalized to the number of bases in the window that were covered at threefold coverage or greater in the SHR/OlaIpcv sequence. (A) Correlation between SNP density and indel density. (B) Correlation between number of deletions per megabase and SNP density. (C) Correlation between number of deletions per megabase and indel density.
