In the SureSelect RNA sequencing runs, all RNA samples were dried by vacuum centrifugation before resuspension using 19 μl RNASeq Fragmentation Mix. Fragmentation, generation of adapter-ligated cDNA libraries, hybridisation, PCR and all post-reaction clean-up steps were performed according to the SureSelectXT Automated RNA Target Enrichment protocol. All recommended quality steps were performed.
Do you have any questions about this protocol?
Post your question to gather feedback from the community. We will also invite the authors of this article to respond.