Hello! Sorry if this has been discussed somewhere already.
I've put together a galaxy pipeline for ChIP-seq analysis and now need to run it on 32 different samples. I've launched it, but matching the file names such as "peaks on data 132" back to originally uploaded fastq files with meaningful names is tedious and almost impossible.
Could you please advise on how to keep meaningful names on all files throughout the analysis?
Thanks in advance Olga