Thank you so much for this amazing normalization tool. I would like to ask, I am currently trying to integrate 5 studies (batches) with varying number of samples (pancreatic cancer). I saw that some samples have lower sequencing depth than others following my QC filtering step.
Therefore, should I perform sctransform per sample, per batch or the merged dataset (all 5 studies, 68 samples).
Hi,
Thank you so much for this amazing normalization tool. I would like to ask, I am currently trying to integrate 5 studies (batches) with varying number of samples (pancreatic cancer). I saw that some samples have lower sequencing depth than others following my QC filtering step.
Therefore, should I perform sctransform per sample, per batch or the merged dataset (all 5 studies, 68 samples).
Thank you!
BW, Constantinos