Entering edit mode
21 months ago
Sebastian Hesse
▴
350
For proteome differential expression analysis I am using LIMMA. The MassSpec data were quantified by MaxQuant and given to me as a table. For graphical analysis (PCA, clustering) I use VSN (variant stabilising) normalised and batch effective t corrected data.
Now I would like to perform differential expression analysis using LIMMA.
Could you advise me if I should use the original data only or e.g., VSN normalised (BUT NOT BATCH CORRECTED) data as input for limma?
Thank you!