Entering edit mode
6.8 years ago
nadia_boufaied
▴
10
Hi I am analysing singleCell RNAseq data, in one batch of cells I have more spike-in than in the others (a different concentration of spike_in has been added to the RNA). I was wondering what is the best procedure to normalise the data to be able to integrete these cells in the analysis Thank you Nadia
