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
Poster )
Detection of alternative isoforms of gene fusions using long-read Nanopore RNA-seq
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?
Brochure )
Brochure: multiomic sequencing
Bioinformatics tool )
AERON: Transcript quantification and gene-fusion detection using long reads
