Dear all , I'm very naive regarding bioinformatic tools. I need to trim my sanger sequences to remove bad quality 5' and 3' ends and then I will join thiese sequences in order to create a long contig ( each PCR is a piece of a viral genome and I need to recostrunct the whole genome starting from these pcr that I have done with a walk by walk strategy). I tried some tools in galaxy but I'm not able to do the quality treaming of my sequences ( in fastqc i ever see the bad quality ends after the use of trimmomatic or trim galore or others tools. could you suggest me -the right way to do that in galaxy -than I would like to use cap3 to crate the contig ( it's ok?)
suggestions thankss a lot! Petrus