Multiomics whole-genome characterisation of a cancer genome using Oxford Nanopore sequencing
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Comprehensive identification of somatic and single nucleotide variants (SNVs), structural variants (SVs), and copy number variants (CNVs), as well as epigenetic modifications (5mC and 5hmC) and chromatin accessibility from a single dataset.
Download the poster to find out about:
- Our end-to-end tumour-normal and tumour-only Oxford Nanopore sequencing workflow
- Accurate identification, phasing and annotation of somatic SNVs
- Purity estimation and joint haplotype-resolved somatic SV and CNV calling
- Multiomics analysis of PTEN in COLO829 including full-length transcriptome sequencing