02 October 2017 1 554 Report

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 

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