Dear scverse team,
I just saw the cellrank tool, and find it very interesting and exciting!
I would like to apply it to one of the data sets and have two questions to the experts:
Does the data need to be in a specific format? Which RNA count data in the h5ad object is used - the processed or the raw counts or? Basically the question is how applicable is it to ‘any’ dataset?
Any objections/ concerns around single cell and single nuclei data sets? Or doesnt it matter?
Thanks a lot and looking forward to your input,