Hi all. i am running qiime2 to analyse bacteria which target v3-v4 region .
What is the reason for such low number of merged and non chimeric sequences?
I looked at this after DADA2 where i trimmed my forward and reverse to around 220?
Hi all. i am running qiime2 to analyse bacteria which target v3-v4 region .
What is the reason for such low number of merged and non chimeric sequences?
I looked at this after DADA2 where i trimmed my forward and reverse to around 220?
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