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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 sensitive 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.
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
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