Resource Centre
369 results
Getting started guide: bulk transcriptomics
- Cancer research
- RNA
- cDNA
- Transcriptome
- Transcriptomics
- Fusion transcript
- Human genomics
- Clinical research
- Splice variation
- Isoforms
- Extraction
- Library prep
- PromethION
December 9 2024
Antibiotic-mediated selection of randomly mutagenised and cytokine-expressing oncolytic viruses
- Cancer research
- Biopharma
- Virus
- MinION
November 28 2024
Rapid intraoperative amplicon sequencing of CNS tumour markers
- Cancer research
- Amplicons
- Flongle
- MinION
November 7 2024
Nanopore sequencing for T-cell receptor rearrangement analysis in cutaneous T-cell lymphoma
- Cancer research
- Human genomics
November 1 2024
Getting started guide: single-cell transcriptomics
- Cancer research
- Single cell
- RNA
- cDNA
- Fusion transcript
- Transcriptome
- Transcriptomics
- Human genomics
- Clinical research
- Variant calling
- Extraction
- Structural variation
- Bioinformatics
- EPI2ME
- Gene expression
- Gene fusions
- Immunology
- Isoforms
- Kits
- Library prep
- P2
- PromethION
- PromethION 2 Integrated
- Sample prep
- SNVs
November 1 2024
Diagnosing intravascular B-cell lymphoma using nanopore sequencing of cell-free DNA from cerebrospinal fluid
- Cancer research
- Human genomics
- Methylation
- MinION Mk1B
October 28 2024
High-resolution measurement of individual telomere lengths with Telo-seq
- Cancer research
- Human genomics
- DNA
October 22 2024
Novel nanopore sequencing method for determining Human Papillomavirus integrations in tumours without the need for whole genome sequencing
- Cancer research
- Human genomics
- Targeted
- Amplicons
- MinION
October 19 2024
Long-read sequencing of an advanced cancer cohort resolves rearrangements, unravels haplotypes, and reveals methylation landscapes
- Cancer research
- PromethION
- Structural variation
- Methylation
- Phasing
- Epigenetics
- Long-read
October 14 2024
Real-time genomic characterisation of paediatric acute leukaemia using adaptive sampling
- Cancer research
- Targeted
- Adaptive sampling
- P2 Solo
- MinION
October 13 2024
Webinar: transforming cancer care - redefining cancer characterisation and predisposition insights through nanopore sequencing
- Cancer research
- Webinar
October 10 2024
The interplay of mutagenesis and ecDNA shapes urothelial cancer evolution
- Cancer research
- Structural variation
- PromethION
- MinKNOW
- Q20+
October 9 2024
Development and extensive sequencing of a broadly-consented Genome in a Bottle matched tumour-normal pair for somatic benchmarks
- Cancer research
- Human genomics
- PromethION
September 22 2024
The potential of therapeutic mRNA — and how to measure it
- Cancer research
- Biopharma
- Clinical research
- MinION
- GridION
- Q-Line
- Targeted
September 18 2024
NESSI-Seq: novel cfDNA methylation assays for biomarker discovery and precision medicine
- Cancer research
- Biopharma
- Bioinformatics
- Human genomics
- PromethION
- Epigenetics
- SNVs
- Phasing
- Structural variation
- Targeted
- Whole genome
September 18 2024
Unraveling gene expression patterns in pediatric germ cell tumors: a nanopore sequencing approach
- Cancer research
- Bioinformatics
- MinION
- Gene expression
- Transcriptomics
September 17 2024
Transforming cancer care: redefining cancer characterization and predisposition insights through nanopore sequencing
- Cancer research
- Human genomics
- MinION
- Flongle
- Epigenetics
- SNVs
- Phasing
- Structural variation
- Targeted
September 17 2024
Showcase: Carrier screening
- Cancer research
- Clinical research
- Bioinformatics
- Human genomics
- Population genomics
- MinION
- GridION
- EPI2ME
- GridION Q
- SNVs
- Phasing
- Structural variation
- Targeted
September 17 2024
Nanopore-based random genomic sampling for intraoperative diagnosis of brain tumors and beyond
- Cancer research
- Clinical research
- Human genomics
- MinION
- P2
- Epigenetics
- Structural variation
- Whole genome
September 17 2024
Diverse structural variants cluster near breakage-fusion-bridge site in cancer genomes
- Cancer research
- Human genomics
- Infectious disease
- Population genomics
- P2
- Assembly
- Fusion transcript
- SNVs
- Phasing
- Structural variation
- Transcriptomics
- Whole genome
September 17 2024