On-demand webinar

Single-cell whole transcriptome analysis using random priming

Perform whole transcriptome analysis with SMART-Seq technology, now with the option for random priming. Our highly senstive SMART-Seq Stranded Kit identifies more genes and yields reproducible results even when starting from as little as 1–1,000 cells. In this short on-demand webinar, our R&D group leader, Dr. Nathalie Bolduc, highlights key benefits and discusses example data obtained with the kit.

Nathalie Bolduc, Ph.D.
R&D group leader

The pairing of random priming with proven SMART-Seq technology enables improved and accurate detection of:

  • coding and noncoding RNA
  • long noncoding RNA with more unique genes
  • non-polyadenylated RNAs