Entering edit mode
3.7 years ago
boymin2020
▴
80
Hi all,
Recently, I have been debugging my pipeline for nanopore sequencing data. The input data provided from my cooperators is hundreds of fastq files. Should I concentrate them to one file with the "cat" shell command for the downstream analysis?
Thanks,
Thank you for your reply. As this is the first step in my pipeline, I think there was no need to post the details here.