Entering edit mode
8.0 years ago
xieshaojun0621
▴
210
Imaging I have a big insertion in the genome. Then if I sequence the sample and align the reads to the reference genome, I will get some split reads. I showed one example here.
My plan is to identify the insertion site using these split reads.
Could anyone give me some suggestions of how to do this?
Thanks. I'll try it.