Hi, I have a question regarding paired end FastQ files. I have two individual seq-round for the Read1 and for the Read2. How can I combine the reads from both of these runs into one outpout to run alignment pipeline? Thanks, Audrey
Use the Dataset Collections functions to run data in batch through tools. An explanation about how to build/use these within Galaxy is in a distinct tutorial, and others often include them in the analysis examples.
Galaxy tutorials: https://galaxyproject.org/learn/
Thanks! Jen, Galaxy team