Dear @davidebolo1993 ,
Thanks your for this useful tool. I have a question about simulating illumina sequencing data using VISOR SHORtS. Firt, using the same insertion bed file for simulating long-read and short-read sequencing data, i found that most of insertion could not be simulated in short-read data, like that
I would say that this is expected since short reads have limitations with large SVs and are splitted at breakpoints. Highlighting soft-clipped bases should help.
Dear @davidebolo1993 , Thanks your for this useful tool. I have a question about simulating illumina sequencing data using VISOR SHORtS. Firt, using the same insertion bed file for simulating long-read and short-read sequencing data, i found that most of insertion could not be simulated in short-read data, like that
![image](https://user-images.githubusercontent.com/47030888/202351332-e65bd45d-b6ec-45a2-858d-3801c5b2bc4f.png)
VISOR HACk -g ref.fa -b ins.bed -o ./ins.hack.out
VISOR SHORtS -s ins.hack.out/ -b shorts.laser.simple.chr1.bed -g ref.fa -o ./SR.ins.laser.out --threads 10 --coverage 50
Do you have any suggestions on that? Thank you so much Lixin