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Taking your single-cell sequencing to new lengths with Oxford Nanopore

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The analysis of genomic heterogeneity at the single-cell level has provided new insights into many research areas, including cancer research, cell development and function, and immunology. However, the use of short-read sequencing limits the ability to identify isoforms, alternative splicing, variants, and other biologically important features. Nanopore sequencing resolves this challenge by enabling the analysis of full-length transcripts to gain a deeper understanding of complex biology.

Join this Knowledge Exchange to learn more about implementing the Oxford Nanopore single-cell sequencing workflow — from library preparation to data analysis — with our in-house experts. The presentations will be followed by a live Q&A session.

You will hear about:

  • Best practices for library preparation with 10x Genomics full-length cDNA

  • Easy-to-implement data analysis with our EPI2ME workflow: wf-single-cell

  • Example data analysis outputs, including UMAPs and tertiary analysis compatible files

Please note, this Knowledge Exchange will broadcast at 7am (GMT)/3pm (SGT) and 4pm (GMT)/12pm (EDT). You can select the one suitable for you below.

Meet the speakers

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