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
