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