Entering edit mode
3.5 years ago
robert.murphy
▴
90
I have a large metagenomic 16S amplicon sequencing dataset and am binning them into ASVs based off a SNP threshold. I want to ensure my binned ASVs are not an artefact of the sequencing error rate.
However I am at a loss as to how I would go about this given there are many parameters that given the error rate for any given run as extensively detailed here
Would anyone have advice on how I can go about determining per amplicon I can expect x number of errors?
How did you get your ASVs? Software like DADA2 or deblur, which perform and ASV-level binning, already try to corrects both PCR and sequencing errors.
Did you sequence, along with your samples, a mock community?