I have scRNA-seq data for 4 groups Treatment 1, Control 1, Treatment 2, Control 2.
My goal is to compare gene expression in each cell type between Treatment 1 and Control 1, between Treatment 2 and Control 2, and between Treatment 1 and Treatment 2.
Should I perform QC, Normalization, and clustering on the combined 4 scRNA-seq datasets and then do DE analysis in each identified cluster?
Any suggestions?
Hello, I have more or less same experimental setting and was wondering how you proceeded with your analysis? Can I reach its GitHub repository to see codes or paper to see comparisons on plots?
Open a new question, with details.