Hello Qiime team,
I am very new to Qiime. I started following different workflows.
The first data-set I am doing hands on is qiime2-moving-pictures-tutorial.
The could follow reproduce most of the steps but I have a question related to biology behind.
Step1: involved importing the data where
--input-path parameter seld recognize the data type (fasta or fastq)
Step2: is demultiplexing using metadafile. Here I have problem. I simply tried to grep the barcode sequences from that raw data but I could not find it. Can you please explain me how barcodes and Primers are used to demultiplex the data?
looking forward for your feedback