Resource Centre
Publication )
Yaniv Erlich: A vision for Ubiquitous Sequencing
Workflow )
Workflow overview: direct RNA sequencing
Workflow )
Workflow overview: bulk transcriptomics
Learning )
Which library prep workflow is right for my experiment?
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
Video )
Unlocking isoform programs underlying brain development with long-read single-cell RNA sequencing | LC26
Poster )
Universal, amplicon-based sequencing method for Canine Morbillivirus (CDV)
Video )
Understanding the role of rRNA modifications in colorectal cancer | LC26
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
