Main menu

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


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.

Watch 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.

Getting started

Buy a MinION starter pack Nanopore store Sequencing service providers Channel partners

Quick links

Intellectual property Cookie policy Corporate reporting Privacy policy Terms & conditions Accessibility

About Oxford Nanopore

Contact us News Media resources & contacts Investor centre Careers BSI 27001 accreditationBSI 90001 accreditationBSI mark of trust
English flag