Resource Centre
Video 
William Jeck: Nanopore sequencing and rapid fusion testing – a ‘killer app’ in molecular pathology
Publication 
Whole-genome sequencing with long reads reveals complex structure and origin of structural variation in human genetic variations and somatic mutations in cancer
Publication 
Whole genome assembly of human papillomavirus by nanopore long-read sequencing
Publication 
In vivo genetic screen identifies a SLC5A3-dependent myo-inositol auxotrophy in acute myeloid leukemia
Publication 
Transcriptome profiling for precision cancer medicine using shallow nanopore cDNA sequencing
Publication 
Transcriptional silencing of ALDH2 in acute myeloid leukemia confers a dependency on Fanconi anemia proteins
Publication 
TP53 gene mutation analysis in chronic lymphocytic leukemia by nanopore MinION sequencing
Publication 
TEQUILA-seq: a versatile and low-cost method for targeted long-read RNA sequencing
Publication 
A survey of rare epigenetic variation in 23,116 human genomes identifies disease-relevant epivariations and novel CGG expansions
Publication 
Suberoyl bis-hydroxamic acid reactivates Kaposi’s sarcoma-associated herpesvirus through histone acetylation and induces apoptosis in lymphoma cells
Case study 
Case study: solving the parent-of-origin effect in retinoblastoma to determine disease severity
Publication Single-molecule RNA sequencing reveals IFNγ-induced differential expression of immune escape genes in merkel cell polyomavirus–positive MCC cell lines
Publication 
Single-cell multi-omics reveals elevated plasticity and stem-cell-like blasts relevant to the poor prognosis of KMT2A-rearranged leukemia
Video 
Simultaneous methylation and chromatin accessibility profiling on breast cancer models
Publication Simultaneous detection and comprehensive analysis of HPV and microbiome status of a cervical liquid-based cytology sample using Nanopore MinION sequencing
Publication 
Short and long-read genome sequencing methodologies for somatic variant detection; genomic analysis of a patient with diffuse large B-cell lymphoma
Publication 
Robust methylation-based classification of brain tumors using nanopore sequencing
Publication Real-time detection of BRAF V600E mutation from archival hairy cell leukemia FFPE tissue by nanopore sequencing
Publication 
Rapid identification of genomic structural variations with nanopore sequencing enables blood-based cancer monitoring
Publication 
Rapid-CNS2: Rapid comprehensive adaptive nanopore-sequencing of CNS tumors, a proof of concept study
