Hi everyone
I have a list of paired-end files from Rad-Seq sequencing, for which the barcode (which were at the start of the sequences) were removed after demultiplexing. I was wondering though, I now intend to use the stacks series for a denovo map, but I noticed that my sequences all start with a part of the restriction site used (eg in my forward sequences it starts with TGCAG, and in reverse with CGG). Should I trim (with trimmomatic by example) my data before proceeding with the Stacks series ?
Thank you in advance!