Hey guys,
I'm simulating SVs on the human genome using svsim. The output files I'm using with vgsim to simulate sequencing reads. I have observed something I cannot make sense of:
depending on whether I use svsim in contig or whole genome mode, the result I get using wgsim on either files differs from each other. Shouldn't both output files from wgsim be completely identical?
Can you guys help me out?