Resource Centre
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
Video )
NCM 2023 Houston: GoT-Splice: unraveling cell-type-specific impact of splicing factor mutations
