Ontology highlight
ABSTRACT: Background
RNA sequencing has become the mainstay for studies of gene expression. Still, analysis of rare cells with random hexamer priming - to allow analysis of a broader range of transcripts - remains challenging.Results
We here describe a tagmentation-based, rRNA blocked, random hexamer primed RNAseq approach (T-RHEX-RNAseq) for generating stranded RNAseq libraries from very low numbers of FACS sorted cells without RNA purification steps.Conclusion
T-RHEX-RNAseq provides an easy-to-use, time efficient and automation compatible method for generating stranded RNAseq libraries from rare cells.
SUBMITTER: Gustafsson C
PROVIDER: S-EPMC10111750 | biostudies-literature | 2023 Apr
REPOSITORIES: biostudies-literature