Resource Centre
27 results
Workflow: single-cell transcriptomics
- Single cell
- Transcriptome
- PromethION
- Cancer research
- Clinical research
- cDNA
- Workflow
- Human genomics
- Splice variation
- Gene fusions
- Gene expression
- Kits
February 20 2024
Third-generation Sequencing Reveals Extensive Polycistronism and Transcriptional Overlapping in a Baculovirus
- Microbiology
- Infectious disease
- RNA
- cDNA
- Transcriptome
- Gene fusions
June 5 2018
Single-cell multi-omics reveals elevated plasticity and stem-cell-like blasts relevant to the poor prognosis of KMT2A-rearranged leukemia
- Clinical research
- Cancer research
- Oncology
- Single cell
- Gene fusions
- RNA
- cDNA
- Targeted
- GridION
December 7 2020
Simultaneously detecting methylation and genetic variations of BCR-ABL1 fusion gene by nanopore Cas9-targeted sequencing
- Cancer research
- Gene fusions
- Targeted
- Methylation
- Epigenetics
- Structural variation
- GridION
June 22 2023
Case study: powered by long nanopore reads, liver transcriptome analysis reveals new clues about cancer
- Cancer research
- Transcriptome
- Isoforms
- Splice variation
- cDNA
- RNA
- Clinical research
- Human genomics
- Gene fusions
February 21 2024
Partner independent fusion gene detection by multiplexed CRISPR-Cas9 enrichment and long read nanopore sequencing
- Targeted
- Gene fusions
- Structural variation
- Human genomics
- Clinical research
- Cancer research
- gDNA
- DNA
- GridION
June 5 2020
NCM 2021: Resolution of complex human papillomavirus and human sequences
- Cancer research
- Clinical research
- Gene fusions
- Gene expression
- Human genomics
- Infectious disease
- Structural variation
- Long-read
- Whole genome
- Nanopore Community Meeting
December 2 2021
NCM 2021: Phasing analysis of lung cancer genomes using PromethION R10.4
- Cancer research
- Gene fusions
- Epigenetics
- Gene expression
- Whole genome
- PromethION
- Nanopore Community Meeting
December 2 2021
NCM 2021: Classification of pediatric acute leukaemia using full-length transcriptomics
- Bioinformatics
- Cancer research
- Clinical research
- Gene fusions
- Gene expression
- Human genomics
- Transcriptome
- MinION
- GridION
- Flongle
- Nanopore Community Meeting
December 2 2021
Nanopore sequencing improves the characterisation of mutations driving blood cancer
- Cancer research
- Targeted
- Gene fusions
- mRNA
- Splice variation
- cDNA
- RNA
June 16 2023
A nanopore sequencing–based assay for rapid detection of gene fusions
- Clinical research
- Human genomics
- Gene fusions
- Targeted
- Cancer research
- Real-time
- RNA
- cDNA
September 28 2018
Nanopore RNA-Seq to HLA genotype and correlate donor HLA expression with flow cytometric crossmatch results - Eric Weimer
- Microbiology
- RNA
- AMR
- Gene expression
- Gene fusions
- Targeted
- Structural variation
- DNA
- Whole genome
- Metagenomics
February 6 2020
Long read sequencing reveals a novel class of structural aberrations in cancers: identification and characterization of cancerous local amplifications
- Clinical research
- Cancer research
- Oncology
- Human genomics
- Long-read
- High-throughput
- PromethION
- gDNA
- DNA
- Structural variation
- SNVs
- Whole genome
- Transcriptome
- Gene fusions
- Epigenetics
- Gene expression
April 29 2019
London Calling 2024 technology update
- Adaptive sampling
- Assembly
- Automation
- Basecalling
- Bioinformatics
- Cancer research
- Chromatin conformation
- Data release
- Data storage
- Development
- Direct analysis
- DNA
- EPI2ME
- Epigenetics
- Flongle
- Flow cell
- Gene expression
- Gene fusions
- GridION
- GridION Q
- High-throughput
- Human genomics
- Identification
- Immunology
- Industrial diagnostics
- Infectious disease
- Isoforms
- Kits
- London Calling
- Long-read
- Methylation
- Microbiology
- Microbiome
- MinION
- MinION Mk1B
- MinION Mk1D
- MinKNOW
- Nanopore Community
- Oncology
- Outbreak
- Phasing
- Plasmid
- Portable
- PromethION
- PromethION 2 Integrated
- Q20+
- Q-Line
- Real-time
- RNA
- Short-read
- SNVs
- Splice variation
- Structural variation
- TurBOT
- 16S
May 24 2024
How to load a Flongle Flow Cell
- London Calling
- Animal
- Microbiology
- Bioinformatics
- Cancer research
- Chromatin conformation
- Clinical research
- Environment
- Epigenetics
- Gene fusions
- Gene expression
- Human genomics
- Identification
- Immunology
- Infectious disease
- Metagenomics
- Microbiome
- Plant
- Population genomics
- Reproductive medicine
- Transcriptome
- Flongle
May 20 2022
Nanopore sequencing of cervical cancers uncovers novel genomic, epigenomic, and transcriptomic features associated with HPV integration events
- Infectious disease
- Human genomics
- Cancer research
- Transcriptome
- Structural variation
- SNVs
- Phasing
- Assembly
- Gene fusions
- Epigenetics
- Bioinformatics
- Whole genome
- Transcriptomics
- PromethION
- London Calling
May 24 2021
A targeted nanopore sequencing-based test method for the rapid diagnosis of drug-resistant TB - Justin O'Grady
- RNA
- cDNA
- Gene expression
- Gene fusions
- Structural variation
- Whole genome
- DNA
- Metagenomics
February 28 2020
Improving nanopore read accuracy with the R2C2 method enables the sequencing of highly multiplexed full-length single-cell cDNA
- RNA
- cDNA
- Transcriptome
- Gene fusions
September 25 2018
High-throughput targeted long-read single cell sequencing reveals the clonal and transcriptional landscape of lymphocytes
- RNA
- cDNA
- Transcriptome
- Gene fusions
- Cancer research
- Oncology
- Long-read
- MinION
- Single cell
July 16 2019
Genomic BCR-ABL1 breakpoint characterization by a multi-strategy approach for personalized monitoring of residual disease in chronic myeloid leukemia patients
- Cancer research
- Oncology
- Human genomics
- Clinical research
- Long-read
- Portable
- Gene fusions
- Scalable
- gDNA
- DNA
- MinION
January 5 2018