Resource Centre
Application note 
Application note: long cDNA sequencing reads enable transcriptome analysis at isoform resolution
Poster 
Poster: open access Oxford Nanopore datasets for reproducible benchmarking, sequence exploration, and testing
Poster 
Poster: EPI2ME end-to-end workflows for biopharma quality control of plasmids and mRNA
Publication 
Contaminating plasmid sequences and disrupted vector genomes in the liver following adeno-associated virus gene therapy
Publication 
Twist-ONT: combining nanopore sequencing with the Twist comprehensive viral research panel
Publication 
RAPID: a targeted long-read RNA workflow for functional resolution of splicing variants in rare disease
Publication 
Nanopore-based RNA methylation profiling of a circulating lung cancer biomarker
Publication 
Long-read transcriptomics of a diverse human cohort reveals ancestry bias in gene annotation
Publication 
Nanopore direct RNA sequencing reveals METTL2A-mediated m3C sites in poly(A) RNA
Publication 
Decoding the human PBMC isonome: isoform-level resolution with single-cell long-read transcriptomics
Poster 
A multi-omic investigation of gene dysregulation in a complex chromothripsis-like translocation event using Oxford Nanopore sequencing
Publication Deep intronic SVA_E insertion identified as the most common pathogenic variant associated with Canavan disease: a diagnostic blind spot
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
Workflow Workflow overview: direct RNA sequencing
Publication 
Deregulating m6A regulators leads to altered RNA biology in glioma cell lines
Publication 
Isoform-level profiling of m6A epitranscriptomic signatures in human brain
White paper 
White paper: RNA and cDNA sequencing
Getting started guide 
Getting started guide: bulk transcriptomics
Publication 
A founder BRCA1 exonic duplication involving breakpoint in T2T reference genome-specific region results in constitutional fusion transcript