Skip to main content
. Author manuscript; available in PMC: 2021 Apr 14.
Published in final edited form as: Nat Methods. 2020 Jun 1;17(6):629–635. doi: 10.1038/s41592-020-0837-5

Extended Data Fig. 1. Sample bioanalyzer traces for libraries from TAP-seq and 10X Genomics.

Extended Data Fig. 1

a. Standard 10X Genomics protocol. b. TAP-seq library using panel 1 and cDNA from 10X Genomics K562 cells as input material. Strong peaks in TAP-seq profile correspond to highly expressed genes in the primer panel (HBG1, HBG2, HBE1), as validated by sub-cloning of bands and Sanger sequencing (not shown). c-f. Remaining target gene panels applied to different cell types and cell lines.