Hi,
I am trying to use doubletFinder package on my scRNAseq data that was obtained after super loading i.e. assumed higher % of doublets. In the package description and real data example the "% doublet formation rate" is set to 7.5% and stated that it needs to be tailored to your own dataset. However, how do you tailor it, are there any clues or tips for that? I would be super grateful for any advice on that. Many thanks in advance!
Hi, I am trying to use doubletFinder package on my scRNAseq data that was obtained after super loading i.e. assumed higher % of doublets. In the package description and real data example the "% doublet formation rate" is set to 7.5% and stated that it needs to be tailored to your own dataset. However, how do you tailor it, are there any clues or tips for that? I would be super grateful for any advice on that. Many thanks in advance!