Resource Centre
28 results
Getting started guide: single-cell transcriptomics
- Gene fusions
- Single cell
- RNA
- cDNA
- Fusion transcript
- Transcriptome
- Transcriptomics
- Cancer research
- Human genomics
- Clinical research
- Variant calling
- Extraction
- Structural variation
- Bioinformatics
- EPI2ME
- Gene expression
- Immunology
- Isoforms
- Kits
- Library prep
- P2
- PromethION
- PromethION 2 Integrated
- Sample prep
- SNVs
November 1 2024
London Calling 2024 technology update
- Gene fusions
- 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
- 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
Brochure: multiomic sequencing
- Gene fusions
- Human genomics
- Clinical research
- DNA
- gDNA
- cDNA
- RNA
- Direct analysis
- Transcriptome
- Epigenetics
- Methylation
- Whole genome
- Splice variation
- Isoforms
- Cancer research
- Single cell
March 13 2024
Case study: powered by long nanopore reads, liver transcriptome analysis reveals new clues about cancer
- Gene fusions
- Cancer research
- Transcriptome
- Isoforms
- Splice variation
- cDNA
- RNA
- Clinical research
- Human genomics
February 21 2024
Workflow: single-cell transcriptomics
- Gene fusions
- Single cell
- Transcriptome
- PromethION
- Cancer research
- Clinical research
- cDNA
- Workflow
- Human genomics
- Splice variation
- Gene expression
- Kits
February 20 2024
Simultaneously detecting methylation and genetic variations of BCR-ABL1 fusion gene by nanopore Cas9-targeted sequencing
- Gene fusions
- Cancer research
- Targeted
- Methylation
- Epigenetics
- Structural variation
- GridION
June 22 2023
Nanopore sequencing improves the characterisation of mutations driving blood cancer
- Gene fusions
- Cancer research
- Targeted
- mRNA
- Splice variation
- cDNA
- RNA
June 16 2023
Detection of alternative isoforms of gene fusions using long-read Nanopore RNA-seq
- Gene fusions
- London Calling
- Splice variation
- Transcriptome
May 19 2023
Detection of alternative isoforms of gene fusions from long-read RNA-seq with FLAIR-fusion
- Gene fusions
- Bioinformatics
- Transcriptome
- Long-read
August 3 2022
How to load a Flongle Flow Cell
- Gene fusions
- London Calling
- Animal
- Microbiology
- Bioinformatics
- Cancer research
- Chromatin conformation
- Clinical research
- Environment
- Epigenetics
- Gene expression
- Human genomics
- Identification
- Immunology
- Infectious disease
- Metagenomics
- Microbiome
- Plant
- Population genomics
- Reproductive medicine
- Transcriptome
- Flongle
May 20 2022
NCM 2021: Resolution of complex human papillomavirus and human sequences
- Gene fusions
- Cancer research
- Clinical research
- 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
- Gene fusions
- Cancer research
- Epigenetics
- Gene expression
- Whole genome
- PromethION
- Nanopore Community Meeting
December 2 2021
NCM 2021: Classification of pediatric acute leukaemia using full-length transcriptomics
- Gene fusions
- Bioinformatics
- Cancer research
- Clinical research
- Gene expression
- Human genomics
- Transcriptome
- MinION
- GridION
- Flongle
- Nanopore Community Meeting
December 2 2021
Nanopore sequencing of cervical cancers uncovers novel genomic, epigenomic, and transcriptomic features associated with HPV integration events
- Gene fusions
- Infectious disease
- Human genomics
- Cancer research
- Transcriptome
- Structural variation
- SNVs
- Phasing
- Assembly
- Epigenetics
- Bioinformatics
- Whole genome
- Transcriptomics
- PromethION
- London Calling
May 24 2021
Single-cell multi-omics reveals elevated plasticity and stem-cell-like blasts relevant to the poor prognosis of KMT2A-rearranged leukemia
- Gene fusions
- Clinical research
- Cancer research
- Oncology
- Single cell
- RNA
- cDNA
- Targeted
- GridION
December 7 2020
Partner independent fusion gene detection by multiplexed CRISPR-Cas9 enrichment and long read nanopore sequencing
- Gene fusions
- Targeted
- Structural variation
- Human genomics
- Clinical research
- Cancer research
- gDNA
- DNA
- GridION
June 5 2020
The architecture of SARS-CoV-2 transcriptome
- Gene fusions
- Microbiology
- Virus
- MinION
- Transcriptome
- Whole genome
- Isoforms
- Long-read
- Methylation
- Epigenetics
- RNA
- cDNA
- Direct analysis
- Infectious disease
March 15 2020
A targeted nanopore sequencing-based test method for the rapid diagnosis of drug-resistant TB - Justin O'Grady
- Gene fusions
- RNA
- cDNA
- Gene expression
- Structural variation
- Whole genome
- DNA
- Metagenomics
February 28 2020
Nanopore RNA-Seq to HLA genotype and correlate donor HLA expression with flow cytometric crossmatch results - Eric Weimer
- Gene fusions
- Microbiology
- RNA
- AMR
- Gene expression
- Targeted
- Structural variation
- DNA
- Whole genome
- Metagenomics
February 6 2020
AERON: Transcript quantification and gene-fusion detection using long reads
- Gene fusions
- RNA
- cDNA
- Gene expression
- Bioinformatics
- Transcriptome
- Long-read
January 27 2020