Fig. 2
From: Resolving complex structural genomic rearrangements using a randomized approach
Overview of computational strategy for identifying SV in whole genome sequences. a SVelter first scans the genome and identifies clusters of aberrant read characteristics. These are used to create a putative set of BP positions. b The segments between BPs are then iteratively rearranged and scored against null models of sequence expectations. c The final converged structure is reported as the predicted structural rearrangement for the region