Closed aquagenomics closed 3 years ago
Hello @aquagenomics , I'm afraid these reads are not output to a file, only the taxonomy of the hits are counted and summarized in the report. You'll have to re-map the reads onto the assembled/reconstructed sequences and extract the unmapped reads.
@HRGV i think we can close this issue as there has been no recent activity
Many thanks for this great tool! I was wondering if it would be possible to extract the read sequences corresponding to those that are summarised in the final table (Taxonomic affiliation of unassembled SSU rRNA reads) of the report? I would like to investigate these further, but I couldn't find these sequences (or their fastq IDs) in any of the output files. Thank you!