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