I got 4 files from illumina:
raw_1.fq.gz [Read 1 sequences with barcodes and primers]
raw_2.fq.gz [Read 2 sequences with barcodes and primers]
1.fq.gz [Read 1 sequences with barcode and primer removed]
2.fq.gz [Read 2 sequences with barcode and primer removed]
Could you please answer my two questions?
First is, while importing data on qiime2, should i use the upper two files with primers as the metadata file has the primer column too?
Second is, Should i use the commands related to Casava 1.8 paired-end demultiplexed fastq for importing data on Qiime2?
Please re-read the Code of Conduct's section on Patience. We strive to respond within one business day, and please remember that this is a free service for all users. One of our moderators will follow up with you when we are able. Thanks for your understanding!