Entering edit mode
3.3 years ago
Denis
▴
310
Hi,
I'm analysing amplicon data for an metagenomics study. I'm wondering if i have to use only read pairs containing primer sequences on the 5' end allowing some proportion of the mismatches in them of course? I think this step could help to remove PCR artifacts from the real biological data. Is it a useful approach for amplicon metagenomics?
