Hi @jairideout Thank you for your response!!
1.How did you generate the two files you’re trying to import? i.e. reference-hit.seqs.fa and reference-hit.biom
my data are demultiplexed merged pair end data, and each sample have one fasta.file or fastq.file.
deblur workflow --seqs-fp 01.CleanData --output-dir clean_data -t 250
2.Can you supply the first few lines of reference-hit.seqs.fa?
yes. the first line are the representative seqs as same as the second line....
For example, >atcg........................
atcg.........................
>ggct........................
ggct.........................
3.Can you run qiime feature-table summarize on the .qza file you imported the .biom file into, and send me the output? That’ll be a single .qzv file.
yes, I have the biom.qzv file, but i can not send you now, tomorrow when i go to the office, i will send it to you.
Thank you again.