Full genome sequencing identifies broad spectrum of genetic variants. (a) Coverage profiles of SHR and BN-Lx. (b) The amount of different types of genomic variants detected in BN-Lx and SHR. (c) The distribution of sizes of indels that were detected. Nd, not determined.
Simonis et al. Genome Biology 2012 13:r31 doi:10.1186/gb-2012-13-4-r31