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.