Resource Centre
Workflow Workflow overview: single-cell transcriptomics
Publication 
Simultaneously detecting methylation and genetic variations of BCR-ABL1 fusion gene by nanopore Cas9-targeted sequencing
Case study Case study: powered by long nanopore reads, liver transcriptome analysis reveals new clues about cancer
Video NCM 2021: Phasing analysis of lung cancer genomes using PromethION R10.4
Case study 
Nanopore sequencing improves the characterisation of mutations driving blood cancer
Video London Calling 2024 technology update
Case study 
Case study: improving the characterisation of acute paediatric leukaemia worldwide
Getting started guide 
Getting started guide: single-cell transcriptomics
Bioinformatics tool 
Detection of alternative isoforms of gene fusions from long-read RNA-seq with FLAIR-fusion
Publication 
Combining panel-based and whole-transcriptome-based gene fusion detection by long-read sequencing
Case study 
Case study: is the end to the diagnostic odyssey within reach?
Bioinformatics tool 
AERON: Transcript quantification and gene-fusion detection using long reads