RNA-seq is an important tool for understanding the complex biology of gene regulation and assists in understanding gene expression from ultra-low, high-quality total RNA or intact cells (both bulk or single cell). Our core SMART and LNA technologies have been incorporated into several of our kits to perform either full-length or 3' differential expression RNA-seq using an oligo(dT) priming approach. This approach allows examination of gene expression of the cell population and provides information about isoforms, splice variants, and SNPs. Automation tools can help facilitate this understanding by giving researchers reliable, efficient, and cost-effective high-throughput methods to process more samples.
Automating full-length single-cell RNA-seq libraries
Register to learn about important considerations for optimizing the automation of single-cell NGS on the Beckman Coulter Biomek.
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