Resource Centre
Publication )
Long-read spatial transcriptomics of patient-derived ccRCC organoids identifies heterogeneity and transcriptional remodelling following treatment
Publication )
RAPID: a targeted long-read RNA workflow for functional resolution of splicing variants in rare disease
Publication )
Long-read transcriptomics of a diverse human cohort reveals ancestry bias in gene annotation
Publication )
Transcriptome-wide profiling of alternative splicing regulators with CRISPore-seq
Publication )
Decoding the human PBMC isonome: isoform-level resolution with single-cell long-read transcriptomics
Publication )
Long-read genome sequencing and multi-omics in ageing and neurodegeneration
Publication )
Identification of non-coding causative variant underlying Warsaw Breakage syndrome using long-read based genomic sequencing and transcriptome analysis
Publication )
Long-read single-cell genome, transcriptome and open chromatin profiling links genotype to phenotypes
Case study )
Case study: unravelling tumour biology with single-cell Oxford Nanopore sequencing
White paper )
White paper: RNA and cDNA sequencing
Getting started guide )
Getting started guide: bulk transcriptomics
Workflow )
Workflow overview: bulk transcriptomics
Publication )
Spatial isoform sequencing at sub-micrometer single-cell resolution reveals novel patterns of spatial isoform variability in brain cell types
Webinar )
Integrative multiomics approaches in oncology and rare disease research
Poster Transcriptome-wide expression and RNA modifications with full-length native RNA and cDNA sequencing
Video )
Towards routine modopathy diagnostics: advances and clinical application of direct RNA sequencing
Video )
Single-cell transcriptome sequencing
Video )
Pediatric leukemias: clinical validation of Oxford Nanopore-based gene expression profiling
Video )
Neural transcriptomic and epitranscriptomic modifications by fentanyl and xylazine
Video )
Nanopore sequencing of intact, aminoacylated tRNA
