I need to analyze full length rRNA 16S sequences obtained from a PacBio machine. In order to check if I can do do it with qiime2 and get ASVs (instead of OTUs), I have check the version of the dada2 package installed within the dada2 plugin (last version of qiime2 available, 2019.1). Apparently the version of dada2 that we have is 1.6.0 (please see shell output below).
In the oficial web of dada2, they announce that it is posible to process dada2 reads after their last version, dada2 1.10 (https://benjjneb.github.io/dada2/index.html).
Sorry for the trivial question, but all this means that currently it is not possible to analize dada2 reads with qiime2-dada2, right? I am a bit confused becasue there are some threads in the qiime2 forum disscussing how to analyze PacBio reads within qiime2.
In case that the above were true, is it posible to use Deblur for PacBio? Any benckmarking analysis/pipeline is available for PacBio in qiime2?
Last question -just to understand things better-, is there any technical reason to dont update the dada2 plugin with the last version of the dada2 package available?
Thanks for all qiime2 and plugins developers and community for your immense contribution!
checking packages in qiime2 2019.1
(qiime2-2019.1) qiime2@qiime2core2019-1:~$ conda list
packages in environment at /home/qiime2/miniconda/envs/qiime2-2019.1:
Name Version Build Channel
q2-dada2 2019.1.0 py36_0 qiime2/label/r2019.1
bioconductor-dada2 1.6.0 r3.4.1_0 bioconda