Resource Centre
Application note 
Application note: long cDNA sequencing reads enable transcriptome analysis at isoform resolution
Learning 
Which library prep workflow is right for my experiment?
Video 
Utility of long-read whole-genome sequencing across diverse clinical genomic investigations: a single- center experience | LC26
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 
Ultra-rapid genomic profiling of pediatric brain tumors using whole-genome and targeted long-read sequencing | LC26
Video 
Translating long-read sequencing into a scalable NHS bioinformatics workflow | LC26
Video 
Third-generation homozygosity analysis | LC26
Video 
Targeted nanopore sequencing for newborn screening in a small population | LC26
Video 
Structural variant discovery in MENA individuals using Oxford Nanopore technology reveals clinically relevant variation | LC26
Learning 
Start the timer: how do I prepare a sequencing library in ten minutes?
Poster 
Poster: resolving challenging medically relevant genes in the human genome with native Oxford Nanopore reads
Video 
Reconstruction of chromosome-scale copy number profiles of tumor genomes with long-read sequencing | LC26
Video 
Rapid diagnosis of acute leukemia with integrated epigenomic and genomic profiling | LC26
Video 
RAPID: a targeted long-read RNA workflow for functional resolution of splicing variants in rare disease | LC26
Video 
Population-scale long-read methylation signatures for rare disease classification | LC26
Video 
Oxford Nanopore sequencing to handle missing heritability in rare diseases | LC26
Video 
Oxford Nanopore sequencing of the UK Biobank | LC26
Video 
Nanopore sequencing enables scalable, end-to-end quality control and capsid library profiling of recombinant AAV vectors | LC26
Video 
Nanopore-only telomere-to-telomere assembly of isochromosome 17q in childhood medulloblastoma | LC26
