Resource Centre
Workflow 
Workflow overview: single-cell transcriptomics
Workflow 
Workflow overview: direct RNA sequencing
Workflow 
Workflow overview: bulk transcriptomics
Publication 
Widespread occurrence of hybrid internal-terminal exons in human transcriptomes
Video 
Webinar: Rapid leukemia classification using nanopore sequencing
Case study 
Wastewater sequencing — an early warning system for infectious disease outbreaks
Publication 
In Vivo Validation of Alternative FDXR Transcripts in Human Blood in Response to Ionizing Radiation
Publication 
Virtual Nanopore Day, Switzerland
Publication 
Virtual Nanopore Day, Singapore
Video 
Virtual Nanopore Day, Michigan
Video 
Virtual Nanopore Day, LA
Publication 
Varicella-zoster virus VLT-ORF63 fusion transcript induces broad viral gene expression during reactivation from neuronal latency
Bioinformatics tool 
Using SPAdes de novo assembler
Publication 
Using nanopore RNA-Seq to HLA genotype and correlate donor HLA expression with flow cytometric crossmatch results
Video 
Using full-length transcript sequencing to reveal the fate of mRNA in aging seeds
Publication 
Using direct RNA nanopore sequencing to deconvolute viral transcriptomes
Publication 
Using deep long-read RNAseq in Alzheimer’s disease brain to assess clinical relevance of RNA isoform diversity
Video 
Uncovering RNA splicing’s cell-specific impact on clonal blood disorders with GoT-Splice
Poster 
Uncovering the full-length extracellular transcriptome in human blood plasma using long-read cDNA sequencing
Case study 
Case study: ultra-rich nanopore data offers unprecedented insights into the transcriptomes of single cells
