Resource Centre
Learning 
Which library prep workflow is right for my experiment?
Video 
Using ultra-long-read Oxford Nanopore sequencing to detect complex structural variants in leukaemia
Video 
Using long-read sequencing for translational health research
Video 
Unlocking isoform programs underlying brain development with long-read single-cell RNA sequencing | LC26
Video 
Understanding population-scale structural variation using long-read genomics | LC26
Video 
Translating long-read sequencing into a scalable NHS bioinformatics workflow | LC26
Publication 
Transcriptome profiling of paediatric extracranial solid tumours and lymphomas enables rapid low‑cost diagnostic classification
Video 
Third-generation homozygosity analysis | LC26
Video 
Third-generation cytogenetic analysis
Publication 
Targeted sequencing and iterative assembly of near-complete genomes
Video 
Targeted nanopore sequencing and an integrated analysis framework for neurogenomic disease | LC26
Video 
Targeted adaptive sampling for pharmacogenomics and genome-wide variant analysis
Publication 
Targeted adaptive sampling enables clinical pharmacogenomics testing and genome-wide genotyping
Video 
Studying disease-causing transposable element insertions using Oxford Nanopore sequencing
Video 
Streamlined glioma diagnosis from FFPE tissue: one assay, lower cost, and faster turnaround time
Video 
Stencilling accessible chromatin fibres reveals haplotype-specific regulation
Learning 
Start the timer: how do I prepare a sequencing library in ten minutes?
Video 
Squiggles to the rescue: metagenomics-based pathogen surveillance | LC26
Video 
Single-molecule DNA methylation reveals unique epigenetic identity profiles of T helper cells
Video 
Single-cell transcriptome sequencing
