Resource Centre
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Workflow overview: single-cell transcriptomics
- PromethION 24/48
- Single cell
- Transcriptome
- Cancer research
- Clinical research
- cDNA
February 24 2025
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Workflow overview: plant genome assembly
- PromethION 24/48
- Assembly
- DNA
- Epigenetics
- Kits
- Library prep
February 17 2025
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The mutational and clonality profile of HGSOC is established early in tumour development and conserved throughout therapy resistance
- PromethION 24/48
- Cancer research
- Long-read
- Structural variation
February 19 2025
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The implementation of genome sequencing in rare genetic diseases diagnosis: a pilot study from the Hong Kong genome project
- PromethION 24/48
- Human genomics
- SNVs
- Structural variation
January 28 2025
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Targeted long-read sequencing as a single assay improves diagnosis of spastic-ataxia disorders
- PromethION 24/48
- Targeted
- Human genomics
- Clinical research
- Long-read
- Variant calling
February 25 2025
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A systematic benchmark of nanopore long-read RNA sequencing for transcript-level analysis in human cell lines
- PromethION 24/48
- Long-read
- Isoforms
- Splice variation
- Transcriptome
- cDNA
March 13 2025
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Structural patterns and transcriptional effects of integrated Epstein-Barr virus revealed by long-read sequencing and RNA-sequencing in NPC
- PromethION 24/48
- Cancer research
- Virus
- Fusion transcript
- Structural variation
February 17 2025
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Singleton rapid long-read genome sequencing as first-tier genetic test for critically ill children with suspected genetic diseases
- PromethION 24/48
- Clinical research
- Human genomics
- Structural variation
February 27 2025
Research focus: pharmacogenomics
- PromethION 24/48
- Clinical research
- Human genomics
- Targeted
- DNA
- Adaptive sampling
March 11 2025
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Rapid brain tumour classification from sparse epigenomic data
- PromethION 24/48
- Cancer research
- Methylation
- cfDNA
- Real-time
- MinION
February 28 2025
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Workflow overview: plant Pore-C
- PromethION 24/48
- Workflow
- Plant
- Assembly
- Library prep
- Bioinformatics
March 18 2022
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Application note: Oxford Nanopore sequencing provides superior MAG recovery and strain-level resolution from a complex microbiome
- PromethION 24/48
- Metagenomics
- Microbiome
- Microbiology
- Infectious disease
- Bacteria
March 17 2025
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NCM 2023 Singapore: Novel algorithms for long read analysis and applications
- PromethION 24/48
- Assembly
- Bioinformatics
- Cancer research
- Human genomics
- Plant
September 27 2023
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NCM 2023 Singapore: Direct detection of DNA modifications in human cancer genomes
- PromethION 24/48
- Bioinformatics
- Cancer research
- Chromatin conformation
- Epigenetics
- Gene expression
September 27 2023
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NCM 2023 Houston: Unraveling complex Mendelian diseases with nanopore sequencing
- PromethION 24/48
- Bioinformatics
- Clinical research
- Human genomics
- SNVs
- Splice variation
December 6 2023
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NCM 2023 Houston: Nanopore sequencing reveal structural heterogeneity in canine osteosarcoma
- PromethION 24/48
- Animal
- Bioinformatics
- Cancer research
- Phasing
- SNVs
December 6 2023
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NCM 2023 Houston: Haplotypes, isoforms, and fusions: towards a richer cancer transcriptome
- PromethION 24/48
- Bioinformatics
- Cancer research
- Human genomics
- Phasing
- SNVs
December 6 2023
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Multisite long-read sequencing reveals the early contribution of somatic structural variations to HBV-related hepatocellular carcinoma tumorigenesis
- PromethION 24/48
- Cancer research
- Virus
- Structural variation
- SNVs
March 4 2025
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Long-read sequencing of 945 Han individuals identifies structural variants associated with phenotypic diversity and disease susceptibility
- PromethION 24/48
- Human genomics
- Structural variation
February 10 2025
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Long read sequencing enhances pathogenic and novel variation discovery in patients with rare diseases
- PromethION 24/48
- Human genomics
- Clinical research
- Long-read
- Structural variation
March 14 2025