I have trouble for importing my fastq files as they are already filtered, trimmed etc I don’t know which command should I use in order to import my data and finish my analysis.
I don’t have access to the raw data so I can’t do the pipeline from the beginning.
Thank you for your help, Amélie.
I think you could import these files with using the
Let me know how well this guide works for you!
Thank you for your reply, but to create the manifest file I have to specify if the reads are forward or reverse. As they are already assembled, I don’t know what I should do…
We have some notes on how to do this import here. @colinbrislawn is correct that you would use the fastq manifest format - you’ll just indicate “forward” for the direction of those files. Let us know if you run into any issues.
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