Resource Centre
Brochure )
Brochure: EPI2ME — data analysis for all levels of expertise
White paper )
White paper: cancer research
Case study )
Case study: accurate identification of cancer-predisposing deep intronic variants in tumour-suppressor genes with Oxford Nanopore sequencing
Case study )
Case study: solving the parent-of-origin effect in retinoblastoma to determine disease severity
Case study )
Case study: improving the characterisation of acute paediatric leukaemia worldwide
Video )
London Calling 2024 technology update
Publication )
TEQUILA-seq: a versatile and low-cost method for targeted long-read RNA sequencing
Publication )
Long-read sequencing of diagnosis and post-therapy medulloblastoma reveals complex rearrangement patterns and epigenetic signatures
Publication )
Transcriptome profiling for precision cancer medicine using shallow nanopore cDNA sequencing
Video )
NCM 2022: Finding the needle — haplotype-resolved discovery and annotation of clinically relevant genetic and epigenetic variants using whole-genome nanopore sequencing
Video )
NCM 2022: Clinical and functional significance of germline variation in cancer susceptibility and disease
Publication )
Rapid-CNS2: Rapid comprehensive adaptive nanopore-sequencing of CNS tumors, a proof of concept study
Publication )
ACME: an Affinity-based Cas9 Mediated Enrichment method for targeted nanopore sequencing
Publication )
Whole genome assembly of human papillomavirus by nanopore long-read sequencing
Publication )
Accurate detection of circulating tumor DNA using nanopore consensus sequencing
Publication Single-molecule RNA sequencing reveals IFNγ-induced differential expression of immune escape genes in merkel cell polyomavirus–positive MCC cell lines
Publication )
Extrachromosomal amplification of human papillomavirus episomes as a mechanism of cervical carcinogenesis
Publication )
Intraoperative DNA methylation classification of brain tumors impacts neurosurgical strategy
Publication )
Nanopore sequencing methods detect cell-free DNA associated with minimal residual disease and central nervous system infiltration in pediatric acute lymphoblastic leukemia
Publication )
High resolution copy number inference in cancer using short-molecule nanopore sequencing
