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
Events )
Virtual Nanopore Day, Switzerland
Events )
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
