How do I analyse my microbiome run 150x2 with 9nt overlap in dada2 denoise_pair, if overlap default is min 12nt?

Hi @c_malossi,

I'm assuming you're doing 515F-806R 2x150 sequencing?

It's pretty widely accepted to just use forward reads for this purpose, so no need to modify the trim length. Here's a more detailed forum post on the issue:

Best,
Justine

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