Hi everybody,
It is my first time that I make DNA libraries for RNA sequencing. After using the ScriptSeq V2 library preparation kit I ended up with the attached results. I have run one sample with different concentrations on the High sensitivity DNA chip. Actually I do not have any idea if these peaks are OK or not.
I would really appreciate if someone gives me an advise or explanation, I am running out of time for this project!
It is my first time that I make DNA libraries for RNA sequencing. After using the ScriptSeq V2 library preparation kit I ended up with the attached results. I have run one sample with different concentrations on the High sensitivity DNA chip. Actually I do not have any idea if these peaks are OK or not.
I would really appreciate if someone gives me an advise or explanation, I am running out of time for this project!
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