Resource Centre
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Assessing the readiness of Oxford Nanopore sequencing for clinical genomics applications
- Variant calling
- Human genomics
- PromethION
- MinKNOW
- SNVs
November 4 2024
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Getting started guide: single-cell transcriptomics
- Variant calling
- Single cell
- RNA
- cDNA
- Fusion transcript
- Transcriptome
November 1 2024
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Benchmarking reveals superiority of deep learning variant callers on bacterial nanopore sequence data
- Variant calling
- Microbiology
- Bacteria
- Whole genome
- MinION
- GridION
October 10 2024
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High-coverage nanopore sequencing of samples from the 1000 Genomes Project to build a comprehensive catalogue of human genetic variation
- Variant calling
- Human genomics
- PromethION
- Methylation
- Structural variation
- Whole genome
October 2 2024
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Long-read whole-genome sequencing-based concurrent haplotyping and aneuploidy profiling of single cells
- Variant calling
- Bioinformatics
- Single cell
- Phasing
- PromethION
September 25 2024
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NCM 2024 technology update
- Variant calling
- Nanopore Community Meeting
- Bioinformatics
- Methylation
- Transcriptomics
- Whole genome
September 16 2024
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Targeted long-read sequencing as a single assay improves diagnosis of spastic-ataxia disorders
- Variant calling
- Targeted
- Human genomics
- Clinical research
- Long-read
- Structural variation
September 6 2024
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DeepSomatic: accurate somatic small variant discovery for multiple sequencing technologies
- Variant calling
- Bioinformatics
- Cancer research
- Phasing
August 19 2024
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Workflow: human variant calling
- Variant calling
- Human genomics
- Clinical research
- Cancer research
- PromethION
- Whole genome
July 5 2024
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Unlocking the banana pangenome: harnessing genetic diversity
- Variant calling
- Plant
- Population genomics
- Phasing
- Assembly
- Bioinformatics
May 24 2024
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Towards personalised medicine for breast cancer in the Caribbean: a pilot study
- Variant calling
- Cancer research
- Population genomics
- PromethION
- EPI2ME
- London Calling
May 24 2024
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Targeted sequencing of the entire blood group genome by adaptive sampling
- Variant calling
- Phasing
- Immunology
- London Calling
May 24 2024
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Shining light on a dark mystery: melanoma in bullhead benthic fish in Lake Memphremagog
- Variant calling
- London Calling
- Animal
- Bioinformatics
- Assembly
- Cancer research
May 24 2024
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Long-read sequencing for pathogenic and novel variation discovery in rare diseases
- Variant calling
- Bioinformatics
- Phasing
- Clinical research
- Human genomics
- Epigenetics
May 24 2024
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Innovating and improving genome diagnostics using targeted long-read sequencing
- Variant calling
- Clinical research
- Human genomics
- GridION
- Adaptive sampling
- London Calling
May 24 2024
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Importance of adaptive sampling in nanopore long-read sequencing in pharmacogenetics
- Variant calling
- Bioinformatics
- Clinical research
- Human genomics
- Epigenetics
- London Calling
May 24 2024
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iDTECT® Integration Site Analysis assay: a paradigm shift for the quality control of biologics in rare diseases
- Variant calling
- Microbiology
- Plasmid
- London Calling
- Animal
- Bioinformatics
May 24 2024
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How to sequence microbial isolates with the NO-MISS workflow
- Variant calling
- Infectious disease
- London Calling
- Microbiology
- Clinical research
- Assembly
May 24 2024
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How to get started with nanopore sequencing and plan your experiment
- Variant calling
- Epigenetics
- Human genomics
- Clinical research
- MinION Mk1B
- GridION
May 24 2024
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How to extract high-quality DNA and RNA
- Variant calling
- Human genomics
- Plant
- Animal
- Microbiology
- Microbiome
May 24 2024