The QIIME2 version I’m using is 2019.10 and the sequences were generated by Novaseq.
May I know does it means my sequences had been quality filtered?
Do I still need to proceed dada2/ deblur?
This doesn't surprise me - the quality profiles for novaseq often look quite different than a miseq run, for example.
Maybe, but the best way to check is to ask your sequencing center.
Most likely, yes - but check with your sequencing center first to see if any quality control or filtering has occurred with these reads - that will impact your decision for DADA2 vs deblur.
May I know are the parameters I chose are good to go?
Besides, I've come across a forum that discussed about the similar issue as I am facing now and It was recommended to enforce monotonicity in the fitted error model by changing the error model matrix. May I know is this a necessary step?
Hi @pyee0417 - unfortunately there isn’t formal support for NovaSeq data with DADA2, so you are on your own there. As suggested in that post you linked to, your best bet will be to run DADA2 in R. Fortunately you already have DADA2 installed in your QIIME 2 environment.