Using qiime (or mothur) with 16S V1-V3 data
I have Illumina PE reads of 16S V1-V3 data. I've already merged the reads and would like to analyse it using Qiime (or mothur). I assume the standard workflows have to be adapted as they rely on 16S V4 databases. Can anyone suggest a workflow which is specifically adjusted for V1-V3 data?
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If your database contains the full sequence of 16S genes then no changes in the workflow would be needed. See for example
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