Hi,
I got these results in tape station (attached).
The small RNA library size should be around 173bp, so I think that libraries 28, 31, 34, 36, 37 also have an adapter dimer.
I am going to allocate about 10M reads per library. Do you think that with this read number, I will have enough small RNA depth even if I sequence the adapter dimers?
I can size-select on a gel but that will force me to do it for all libraries and I wish to avoid that.
What is your advice?
Iddo