Resource Centre
Publication 
Exon skipping as a potential diagnostic biomarker in colorectal cancer: an integrated epigenomic-transcriptomic analysis
Publication 
Long-read spatial transcriptomics of patient-derived ccRCC organoids identifies heterogeneity and transcriptional remodelling following treatment
Publication 
Transcriptional readthrough precedes alternative splicing programs triggered in CML cells by imatinib
Publication 
Nanopore sequencing reveals novel alternative splice variants of EZH2 in paediatric medulloblastoma
Workflow 
Workflow overview: direct RNA sequencing
Publication 
A single-cell, long-read, isoform-resolved case-control study of FTD reveals cell-type-specific and broad splicing dysregulation in human brain
Getting started guide 
Getting started guide: bulk transcriptomics
Publication 
Single-cell and spatial alternative splicing analysis with nanopore long-read sequencing
Publication 
A systematic benchmark of nanopore long-read RNA sequencing for transcript-level analysis in human cell lines
Publication 
Targeted long-read sequencing as a single assay improves diagnosis of spastic-ataxia disorders
Workflow 
Workflow overview: single-cell transcriptomics
Brochure 
Brochure: multiomic sequencing
Publication 
MrHAMER2: high-accuracy long-read RNA sequencing to decode isoform-specific variation in viral transcripts during latency
Publication 
Genetic regulation of nascent RNA maturation revealed by direct RNA nanopore sequencing
Publication 
Applications of nanopore sequencing in precision cancer medicine
Video 
London Calling 2024 technology update
Case study 
Case study: mapping RNA modifications in the human brain with full-length transcript sequencing
Case study 
Case study: powered by long nanopore reads, liver transcriptome analysis reveals new clues about cancer
Video 
NCM 2023 Houston: Unraveling complex Mendelian diseases with nanopore sequencing
Video 
NCM 2023 Houston: Haplotypes, isoforms, and fusions: towards a richer cancer transcriptome
