I am analysing data which I have mapped to the reference genome using HISAT2. I estimated the expression using Stringtie.
Now I want to run DESeq2 on this data. Works well so far. But I am not sure how I have to "model" my experimental design.
I have:
- 5 x biol. replicates "Control (no treatment)"
- 5 x biol. replicates "Treatment low dosage (chemical compound)"
- 5 x biol. replicates "Treatment high dosage (chemical compound)"
Do I have to compare control<>low dosage
and control<>high dosage
individually or is there a better way to model the "gradient" of treatment using DESEq2?