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
