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Hi,
I am trying to generate an OTU table using SingleM, but I think I am using the wrong command.
I ran:
singlem pipe
--reads sample_R1.fastq.gz sample_R2.fastq.gz
--otu-table output_directory/sample_OTUtable.csv
--threads 16
I expected an OTU table, but instead I got output like this:
gene sample sequence num_hits coverage taxonomy
This looks like gene-level sequence hits, not an OTU table.
Also, the genes are not unique, which makes me think something is wrong.
My question:
How should I correctly run SingleM to generate an OTU table?
Thank you!
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