Resource Centre
Publication 
Yaniv Erlich: A vision for Ubiquitous Sequencing
Workflow Workflow overview: direct RNA sequencing
Workflow 
Workflow overview: bulk transcriptomics
Case study 
Wastewater sequencing — an early warning system for infectious disease outbreaks
Publication 
Utilising nanopore direct RNA sequencing of blood from patients with sepsis for discovery of co- and post-transcriptional disease biomarkers
Bioinformatics tool 
Using SPAdes de novo assembler
Video 
Using nanopore sequencing for mRNA vaccine quality control: a journey from R&D to GMP
Publication 
Using deep long-read RNAseq in Alzheimer’s disease brain to assess clinical relevance of RNA isoform diversity
Video 
Unraveling gene expression patterns in pediatric germ cell tumors: a nanopore sequencing approach
Poster 
Unlocking Nanopore sequencing for managing food safety in the food industry
Poster 
Universal, amplicon-based sequencing method for Canine Morbillivirus (CDV)
Poster 
Uncovering the full-length extracellular transcriptome in human blood plasma using long-read cDNA sequencing
Bioinformatics tool 
Two-pass alignment using machine-learning-filtered splice junctions increases the accuracy of intron detection in long-read RNA sequencing
Publication 
Transcriptome-wide profiling of alternative splicing regulators with CRISPore-seq
Poster 
Transcriptome-wide expression and RNA modifications with full-length native RNA and cDNA sequencing
Publication 
Transcriptome variation in human tissues revealed by long-read sequencing
Publication 
Transcriptome profiling for precision cancer medicine using shallow nanopore cDNA sequencing
Publication 
Transcriptome profiling of paediatric extracranial solid tumours and lymphomas enables rapid low‑cost diagnostic classification
Poster 
Transcriptome profiling of Korean colon cancer by cDNA PCR Nanopore sequencing
Poster 
Transcriptome analysis using long nanopore reads