Resource Centre
15 results
NCM 2023 Houston: Enrichment strategies for recovery of Avian influenza virus from samples using MinION
- EPI2ME Labs
- Infectious disease
- Metagenomics
- Microbiology
- MinION
- EPI2ME
- Nanopore Community Meeting
December 6 2023
Workflow: plasmid sequencing
- EPI2ME Labs
- Bioinformatics
- Workflow
- EPI2ME
- Bacteria
- Microbiology
- Infectious disease
August 15 2023
Core lab webinar series: A new 'gold standard' solution for complete plasmid sequencing
- EPI2ME Labs
- Microbiome
- Infectious disease
July 28 2023
London Calling 2023: Tuberculosis drug resistance profiling from native sputum using nanopore targeted sequencing: a field application study
- EPI2ME Labs
- Clinical research
- Infectious disease
- Microbiology
- Targeted
- MinION
- London Calling
May 19 2023
London Calling 2023: Leveraging Nextflow for the analysis of anything, anywhere, by anyone
- EPI2ME Labs
- Bioinformatics
- EPI2ME
- London Calling
May 19 2023
London Calling 2023: How to take your data analysis further
- EPI2ME Labs
- Assembly
- Bioinformatics
- Chromatin conformation
- Clinical research
- Epigenetics
- Gene expression
- Human genomics
- Infectious disease
- Metagenomics
- Microbiology
- Microbiome
- Phasing
- Single cell
- EPI2ME
- London Calling
May 19 2023
London Calling 2023: How to get started with data analysis
- EPI2ME Labs
- Bioinformatics
- Clinical research
- Epigenetics
- Human genomics
- EPI2ME
- Q20+
- London Calling
May 19 2023
London Calling 2023: Detection and differentiation of respiratory viral pathogens using near real-time sequencing
- EPI2ME Labs
- Assembly
- Bioinformatics
- Infectious disease
- Microbiology
- Microbiome
- SNVs
- Structural variation
- Targeted
- MinION
- GridION
- Flongle
- VolTRAX
- EPI2ME
- London Calling
May 19 2023
Protocol overview: whole human genome sequencing on PromethION
- EPI2ME Labs
- PromethION
- Human genomics
- Whole genome
- Variant calling
- Structural variation
- SNVs
- Methylation
- EPI2ME
- Epigenetics
- gDNA
- Sample prep
- Library prep
- Bioinformatics
- Clinical research
- Population genomics
- High-throughput
May 15 2023
NCM 2022: How to generate assemblies and call variants
- EPI2ME Labs
- Assembly
- Bioinformatics
- Gene expression
- Human genomics
- Metagenomics
- Microbiology
- Single cell
- SNVs
- Phasing
- Transcriptome
- Whole genome
- EPI2ME
- Nanopore Community Meeting
December 7 2022
NCM 2022: How to basecall your data and detect methylation
- EPI2ME Labs
- Assembly
- Cancer research
- Epigenetics
- Human genomics
- Bioinformatics
- Targeted
- Clinical research
- EPI2ME
- Q20+
- Nanopore Community Meeting
December 7 2022
NCM 2022: Can nanopore long-read sequencing replace current cytogenetic methods in clinical genetic diagnostics?
- EPI2ME Labs
- Bioinformatics
- Clinical research
- Structural variation
- Whole genome
- PromethION
- EPI2ME
December 7 2022
NCM 2022: Harnessing automation and integrated solutions to enable nanopore sequencing at any scale
- EPI2ME Labs
- Bioinformatics
- PromethION
- EPI2ME
- Nanopore Community Meeting
December 7 2022
Generating assemblies and calling variants
- EPI2ME Labs
- London Calling
- Assembly
- Bioinformatics
- Structural variation
- EPI2ME
May 20 2022
Plasmid sequencing, assembly and analysis workflow
- EPI2ME Labs
- Bioinformatics
- Bacteria
- EPI2ME
February 15 2022