Hey Qiime2 Community!
I am trying to create a fasta file from a .qza file. I am trying to compare a bunch of samples from different primer sets so I am trimming them first with cutadapt and then need the fasta file. I am using Qiime2 version 2024.5. I uploaded the fasta sequences with these commands:
qiime tools import --type SampleData[SequencesWithQuality] --input-path $1 --output-path 2_demux_output_file.qza --input-format SingleEndFastqManifestPhred33V2
and then trimmed the reads using:
qiime cutadapt trim-single --i-demultiplexed-sequences 2_demux_output_file.qza --p-adapter TTACCGCGGCKGCTGRCAC ATTAGAWACCCBNGTAGTCC --p-match-read-wildcards --p-match-adapter-wildcards --verbose --o-trimmed-sequences trimmed_remove_primers_wild.qza
qiime cutadapt trim-single --i-demultiplexed-sequences trimmed_remove_primers_wild.qza --p-front GTGYCAGCMGCCGCGGTAA GGACTACNVGGGTWTCTAAT --p-match-read-wildcards --p-match-adapter-wildcards --p-discard-untrimmed --verbose --o-trimmed-sequences primers_removed_final.qza
And then I try to visualize it with:
qiime demux summarize --i-data primers_removed_final.qza --o-visualization trimmed_4_demux_output_visfile.qzv
But this does not provide me with the fasta file. I do not want to run DADA2 or Deblur on the sequences (I know how to get sequence files after running those commands) because I just want to look at them post trim from this file. How to I get the fasta file from primers_removed_final.qza? I don't need the count file or anything. Just the fasta file created. Any help would be greatly appreciated. Thanks
Hannah