I have run 3 sample using TruSeq genomic prep using both gel and non gel based methods. The resulting libraries when run on a bioanalyzer all looked like lane 6 of the attached document. Other libraries from the same order looked fine. The input DNA was of sufficient quantity and looked fine on a gel. I have also seen this pattern with one TruSeq RNA library prep sample. Has anyone else seen this?
Thanks,
Mike
Thanks,
Mike
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