Hello everyone!
I am new to handling ONT sequencing data. I am working with a fungus, and the MinION sequencing of its DNA resulted in 80 separate .fastq files (total: 17 GB).
My question concerns the initial Quality Control (QC) step using FastQC. Option A: Should I run FastQC on each of the 80 individual files, or Option B: Should I concatenate (merge) all 80 files into a single .fastq file and run FastQC only once?
Which workflow (A or B) is the most recommended at this point, before the genome assembly stage?"
I got it, thank you so much!! It helped a lot :)