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,
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boymin2020 •
We obviously don't know your pipeline, but indeed you can just concatenate the fastq files (or fastq.gz files) to a single file with cat.
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.
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