Hi there,
I was able to generated loom file from my fastq ran by 10X, but looking at the .out log, there was a warning "no ambient RNA beads were found; maybe sample had too few cells?"
Should we worry or do something about this? And, what would be the impact of this in the downstream analysis or interpretation of the results?
Thank you so much for your help!
Hi there,
I was able to generated loom file from my fastq ran by 10X, but looking at the .out log, there was a warning "no ambient RNA beads were found; maybe sample had too few cells?"
Should we worry or do something about this? And, what would be the impact of this in the downstream analysis or interpretation of the results?
Thank you so much for your help!