Is there any way to generate a taxonomy table for all sequences through Mothur, using the one generated by Classify.seqs?
Following the Mothur SOP, I generated taxonomy for the unique sequences, but I’m interested in having a table for all the quality reads, and I’d prefer not to reclassify 12 million reads if I can avoid it.
I am trying to see the effects of doing some 3’ pre-trimming on the paired .fastq files, and comparing it without any preprocessing using the vanilla MiSeq SOP. I am hoping to be able to generate .taxonomy for every redundant fasta sequence in both datasets, and parsing out the trimmed-vs-vanilla differences read-by-read.
Many Thanks!