Resource Centre
Publication 
Transcriptome profiling for precision cancer medicine using shallow nanopore cDNA sequencing
Publication 
TEQUILA-seq: a versatile and low-cost method for targeted long-read RNA sequencing
Case study 
Case study: solving the parent-of-origin effect in retinoblastoma to determine disease severity
Video NCM 2022: Finding the needle — haplotype-resolved discovery and annotation of clinically relevant genetic and epigenetic variants using whole-genome nanopore sequencing
Publication 
Long-read sequencing of diagnosis and post-therapy medulloblastoma reveals complex rearrangement patterns and epigenetic signatures
Video London Calling 2024 technology update
Bioinformatics tool 
IsoTV: processing and visualizing functional features of translated transcript isoforms
Publication 
Intraoperative DNA methylation classification of brain tumors impacts neurosurgical strategy
Case study 
Case study: improving the characterisation of acute paediatric leukaemia worldwide
Case study 
Case study: accurate identification of cancer-predisposing deep intronic variants in tumour-suppressor genes with Oxford Nanopore sequencing
White paper 
White paper: cancer research