Haplotype-resolved analysis of cancer genomes and epigenomes using Oxford Nanopore sequencing

Comprehensive identification of somatic and germline single nucleotide variants, structural and copy number variants as well as epigenetic modifications (5mC and 5hmC) from a single dataset.

Download the poster to find out:

  • More about our end-to-end tumour-normal nanopore sequencing workflow
  • How it accurately identifies somatic single nucleotides and structural variation
  • How to jointly characterise genomic and epigenomic variants using a single dataset
  • More about genome-wide base-pair resolution 5mC and 5hmC profiling in cancer