Hello Qiime2 Community! I’m beginner in qiime2.
So, I have a question: I did my 16S rRNA sequencing using a kind of primier to bacteria and archaea. In this situation I did the qiime analysis using DADA2 and taken a table.tsv with all ASV to bacteria and archaea. But now, I want to analyze separately these two groups. There one way to separe this information in the DADA2 process? Or past the end analysis?