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Dear Support Team,
I have RNA-seq data from 50 samples. I would like to run RUVSeq to correct the unwanted variables. I wonder if there is a general guide about how to choose k number during RUVg? The online documentation used 1, but I saw some discussion about using other numbers...
Thanks a lot!
C.
Thank you for the quick response!
I saw an general increase in within sample dispersion on PCA plot with increased k. Also, when k=1, the within sample dispersion increases when compared with non-corrected sample. Is it normal?
Thanks a lot!
C.