Creation of consensus sequence #2
Description
Hello,
I have from nanopore technology reads that I want to trim the primers with your algorithm. Is strictly necessary for use it, create previously the consensus sequence for each sample? Or could be work without the consensus sequence per sample?.
I'm trying to understand the function of the consensus sequence into the analysis. Save time in the analysis or something more important?
In my case are short read (from 250 to 500 bp) is a little complicate create the consensus sequence per sample, because I have DNA from different species per sample.
Thank you very much in advantage