Resource Centre
Workflow )
Workflow overview: tumour-normal sequencing
Workflow )
Workflow overview: single-cell transcriptomics
Workflow )
Workflow overview: human variant calling
Workflow )
Workflow overview: bulk transcriptomics
Publication )
The whole is greater than the sum of its parts: long-read sequencing for solving clinical problems in haematology
Publication )
Whole genome sequencing reveals virulence potentials of Helicobacter pylori strain KE21 isolated from a Kenyan patient with gastric signet ring cell carcinoma
Publication )
Whole-genome sequencing with long reads reveals complex structure and origin of structural variation in human genetic variations and somatic mutations in cancer
Video )
Whole-genome insights: nanopore sequencing in neuropathology
Publication )
Whole genome assembly of human papillomavirus by nanopore long-read sequencing
Video )
Transforming tumor methylation profiling with Oxford Nanopore direct DNA sequencing
Webinar )
Transforming hereditary cancer sequencing with adaptive sampling target enrichment
Video )
Resolving complex genomic structures and regulation patterns in cervical cancer
Video )
Webinar: Rapid leukemia classification using nanopore sequencing
Video )
Parent-of-origin-aware genomic analysis infers segregation of pathogenic variants
Video )
Nanopore sequencing: insights from neonatal intensive care to cancer
Video )
Investigating epigenomic alterations in cancer with nanopore sequencing
Video )
Detecting, classifying, and monitoring CNS tumors with nanopore sequencing
Video )
Analysing complex somatic rearrangements in cancer using nanopore sequencing
Video )
Advancing long-read de novo genome assembly methods in clinical research
Knowledge exchange Adaptive sampling explained: the future of flexible target enrichment
