Hi,
My dataset contains single-cell data with the following 6 treatments:
A
A+B
A+B+C
A+C
A+C+D
A+B+C+D
I would like to know the genes specifically induced by B. I wonder if it is okay and more robust to perform pairwise comparisons as below and get the aggregated output of significant genes induced by B in all conditions?
A vs A+B
A+C vs A+C+B
A+C+D vs A+C+D+B
Thanks!