Resource Centre
Poster )
Poster: resolving challenging medically relevant genes in the human genome with native Oxford Nanopore reads
Poster )
Poster: rapid whole-genome sequencing, de novo assembly, and characterisation of bacterial isolates
Poster )
Poster: structural and epigenetic characterisation of D4Z4 arrays in FSHD using Oxford Nanopore multiomic sequencing
Poster )
Poster: rapid and scalable whole-genome microbial isolate sequencing
Poster )
Poster: Oxford Nanopore Adaptive Sampling for tumour-only SNV, SV, and CNV profiling in one assay
Poster )
Poster: digital panels enable targeted enrichment of haematological cancer-associated genomic regions during sequencing
Poster )
Poster: comprehensive resolution of challenging genomic variants with Oxford Nanopore de novo genome assemblies
Poster Poster: open access Oxford Nanopore datasets for reproducible benchmarking, sequence exploration, and testing
Poster )
Poster: genomic insights into the biology of complex microbiomes with Oxford Nanopore metagenomic sequencing
Poster )
Poster: comprehensive pharmacogenomics profiling using Oxford Nanopore digital panels or hybridisation capture
Poster )
Poster: EPI2ME end-to-end workflows for biopharma quality control of plasmids and mRNA
Poster )
Poster: EPI2ME – an extensible product for applied bioinformatics to make sense of your sequencing
Poster )
Poster: end-to-end workflow for haplotype-resolved genetic and epigenetic variant calling using Oxford Nanopore sequencing
Poster )
Poster: performance of Oxford Nanopore whole-genome methylation sequencing in human genetics applications
Poster )
Poster: structural and epigenetic profiling of D4Z4 arrays in FSHD using Oxford Nanopore sequencing
Poster )
Poster: DNA extraction from dried blood spots for Oxford Nanopore sequencing
Poster Scalable pharmacogenomics (PGx) using targeted long-read genotyping panels
Poster )
Resolving challenging medically-relevant genes using nanopore sequencing
Poster A multi-omic investigation of gene dysregulation in a complex chromothripsis-like translocation event using Oxford Nanopore sequencing
Poster )
Comprehensive resolution of challenging genomic variation with Oxford Nanopore telomere-to-telomere assemblies
