I'm looking for some help analysing the profile of a 10x genomics 3' scRNA library prep, run on a 1-6000bp HS fragment analyser (attached pic). The second of my libraries doesn't have a 'smooth' profile and I was hoping for some insight as to why this might be! Will it affect sequencing?
For reference, this data was obtained from differentiating hiPSCs at different time-points.
Thanks!
For reference, this data was obtained from differentiating hiPSCs at different time-points.
Thanks!
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