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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.

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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.