- Product line overview
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- DNA-seq protocols
- Sign up: Total RNA sequencing of liquid biopsies
- Sign-up: MeD-Seq, a novel method to detect DNA methylation
- Sign up: automating full-length single-cell RNA-seq libraries
- Sign up: single-cell DNA-seq webinar
- Sign up: single-cell whole transcriptome analysis
- Single-cell RNA-seq
- Total RNA-seq
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- Targeted RNA-seq
Sign up to view our 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 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
Sign up to watch the video!
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