Trying to figure out Quality Control for RNA-SEQ. I ran FASTQC on the first batch and the same sample, forward strand looks the same as on each lane. The same with the reverse. Is this normal?
Plus it looks kind of like this:
![I have a huge peak on per sequence GC content]
![enter image description here]
Per base and per sequence quality score look alright.
I read all over the internet but those problems seem to be too specific.