Hi @fbeghini
I have a few questions again regarding the additional analysis and arguments:
-
If I want normalized output profiles(normalized in terms of metagenome sizes of fastq files) then would it be okay to use *marker_ab_table?
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–nreads: I have paired end fastq files and suppose that forward end file has 70 reads and reavers end has 70 so shall I put --nreads as 140 or just 70?
Thanks
Saraswati