Join our upcoming webinar to see how seqWell’s plexWell technology has benefited Addgene and the fight against COVID19. Click HERE to register today!




Sequencing of transcripts from single cells has emerged as a powerful tool for understanding the heterogenenous nature of cell function.

Current approaches to single-cell RNAseq (scRNA-seq) vary from single cell encapsulation and 3’-end sequencing to partitioning of single cells and sequencing full length cDNA. seqWell’s normalizing NGS library preparation technology, plexWell™, has shown to improve full-length scRNA-seq analysis.

Looking for more information?

For more information about our plexWell kits used with amplified cDNA, please email us at [email protected] to work with one of our product specialists.

scRNA-Seq Resources

Learn more about this highlighted sequencing application from our 2019 AGBT poster:

AGBT 2019 plexWell scRNA-Seq Poster