I'm wondering if this pipeline will work if my reads contains only UMI at one end?
What read structure is needed to run this successfully?
My current read looks like [Nanopore primer] -- [barcode] -- [custom primer] -- [ds-cDNA insert] -- [TSO/UMI] -- [barcode] -- [Nanopore primer].
How should I adjust the config to run this?
Hi team,
I'm wondering if this pipeline will work if my reads contains only UMI at one end? What read structure is needed to run this successfully? My current read looks like [Nanopore primer] -- [barcode] -- [custom primer] -- [ds-cDNA insert] -- [TSO/UMI] -- [barcode] -- [Nanopore primer]. How should I adjust the config to run this?
Thank you.
Alex