Resource Centre
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Workflow Tumour Normal Sequencing
- Workflow
- Structural variation
- SNVs
- Epigenetics
- Methylation
- Cancer research
August 4 2023
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Workflow Structural Variation
- Workflow
- Structural variation
- PromethION
- Human genomics
- Library prep
- Bioinformatics
November 10 2023
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Workflow Single Cell Transcriptomics
- Workflow
- Single cell
- Transcriptome
- PromethION
- Cancer research
- Clinical research
February 20 2024
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Workflow Plasmid Sequencing Best Practice Workflow
- Workflow
- Bioinformatics
- EPI2ME
- EPI2ME Labs
- Bacteria
- Microbiology
August 15 2023
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Workflow Large Cohort Sequencing
- Workflow
- Human genomics
- Clinical research
- Population genomics
- Whole genome
- Structural variation
October 12 2023
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Workflow Characterising Structural Variants Ffpe Cancer Research Samples
- Workflow
- Cancer research
- Clinical research
- Whole genome
- Human genomics
- Sample prep
July 8 2022
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Workflow: SNV calling and phasing
- Workflow
- Human genomics
- Whole genome
- SNVs
- Structural variation
- Phasing
September 19 2022
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Scywalker: scalable end-to-end data analysis workflow for long-read single-cell transcriptome sequencing
- Workflow
- Single cell
- Transcriptome
- Transcriptomics
- Scalable
- Long-read
September 10 2024
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Overview Influenza Virus Whole Genome Sequencing
- Workflow
- Microbiology
- Infectious disease
- Virus
- Targeted
- Whole genome
August 18 2023
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NCM 2024 technology update
- Workflow
- Nanopore Community Meeting
- Bioinformatics
- Methylation
- Transcriptomics
- Whole genome
September 16 2024
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Workflow: human genome assembly
- Workflow
- Long-read
- PromethION
- Human genomics
- Assembly
- Whole genome
December 15 2022
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Easy transfer of routine, day-to-day sequencing applications to the Oxford Nanopore platform
- Workflow
- EPI2ME
- London Calling
May 21 2024
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