Hi, sorry I am a little confused, and I think the documentation has been updated.
If I am planning on running this pipeline on Takara SMART-BCR with UMIs. I think that I use the clontech_umi_bcr in the profile option.
Do I need to provide any other parameters - previously there was an expectation to use c-primers and linker sequences.
I plan to run this on a HPC, using singularity via SLURM - the FASTQ files total a size of around 60gb, and was run on a P2 flow cell. Is there any guidance on the amount of resources I need to request on the HPC to process this?
Thank you in advance for the advice.