Despite the known relevance of genomic structural variants to pathogen behavior, cancer, development, and evolution, certain repeat based structural variants may evade detection by existing high-throu
The table shows for each sample the number of read pairs in unusual configuration indicating putative DNA sequence rearrangements. Dashes (-) indicate that no read pairs supported a sequence rearrange
Input data and bash scripts to create coordinates of segments on reference sequences. Usage:1. decompres and untar .gz files2. run get_ind_cov.sh - produces coverage files for each species2. run se
