Hi,
I am attempting to import a fastq file that appears to have sequences for multiple samples (this is from a published study where they analyzed using QIIME1). While I have both reverse and forward fastq files from NCBI/SRA, I don't have a barcodes file that i can use to demultiplex. The study provides a mapping file that looks like it was used in QIIME1 importing step, but is a tsv file that includes the headers sample, barcode sequence, linker primer sequence, reverse primer and some other descriptive metadata (see screenshot attached). Can this mapping file be used to demultiplex on QIIME2?
Thanks!