Clone-and haplotype-specific copy number variation inference in heterogeneous bulk tumour samples
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Characterise haplotype-specific large-scale copy number variations (CNVs) and novel hypo/hypermethylation in heterogeneous tumours via whole-genome nanopore sequencing.
Download the poster to discover:
- How cancer progression is associated with the accumulation of somatic mutations and clonal expansion
- A CNV analysis workflow using whole-genome nanopore sequencing, including allele phasing
- How long, direct nanopore sequencing reads facilitate haplotype-specific CNV and methylation analysis in tumour samples
