Resource Centre
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Single laboratory evaluation of the Q20+ nanopore sequencing kit for bacterial outbreak investigations
- Whole genome
- Infectious disease
- GridION
- Long-read
- Bacteria
November 5 2024
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Pushing the boundaries of rare disease diagnostics with the help of the first Undiagnosed Hackathon
- Whole genome
- Human genomics
- RNA
- DNA
October 21 2024
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Benchmarking reveals superiority of deep learning variant callers on bacterial nanopore sequence data
- Whole genome
- Microbiology
- Bacteria
- Variant calling
- 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
- Whole genome
- Human genomics
- PromethION
- Methylation
- Structural variation
- Variant calling
October 2 2024
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The rapid detection of a neonatal unit outbreak of a wild-type Klebsiella variicola using decentralised Oxford Nanopore sequencing
- Whole genome
- Infectious disease
- Bacteria
- MinION
- MinKNOW
October 1 2024
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Complex genetic variation in nearly complete human genomes
- Whole genome
- Human genomics
- PromethION
September 25 2024
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Precision cell engineering enabled through nanopore sequencing
- Whole genome
- Biopharma
- Bioinformatics
- P2
- Assembly
- Epigenetics
September 18 2024
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NESSI-Seq: novel cfDNA methylation assays for biomarker discovery and precision medicine
- Whole genome
- Biopharma
- Cancer research
- Bioinformatics
- Human genomics
- PromethION
September 18 2024
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Implementation of sequencing in a regulated environment
- Whole genome
- Biopharma
- Infectious disease
- Microbiology
- MinION
- GridION
September 18 2024
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Antibody discovery through post-vaccination single-cell transcriptomics and haplotype-resolved germline sequencing
- Whole genome
- Biopharma
- Clinical research
- Bioinformatics
- Human genomics
- Infectious disease
September 18 2024
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Use of Oxford Nanopore sequencing to evaluate potential transmission of hospital infections
- Whole genome
- Infectious disease
- Microbiology
- MinION
September 17 2024
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Understanding the binding of multiple transcription factors by base-pair-resolution chromatin accessibility
- Whole genome
- Clinical research
- Bioinformatics
- Human genomics
- MinION
- Chromatin conformation
September 17 2024
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Ultra-rich human data — variant analysis with EPI2ME
- Whole genome
- Bioinformatics
- Human genomics
- Population genomics
- EPI2ME
- Epigenetics
September 17 2024
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Studying disease-causing polymorphic transposable element insertions using nanopore sequencing
- Whole genome
- Human genomics
- Epigenetics
- Gene expression
- Targeted
September 17 2024
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Resolving structural configurations of DMD intragenic duplications through nanopore long-read sequencing
- Whole genome
- Clinical research
- Bioinformatics
- Human genomics
- PromethION
- Structural variation
September 17 2024
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Positional mapping of active versus silenced rRNA gene clusters within A. thaliana nucleolus organizer regions
- Whole genome
- Bioinformatics
- Plant
- GridION
- Assembly
- Chromatin conformation
September 17 2024
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Obtaining reference genomes of emblematic and endangered Ecuadorian species
- Whole genome
- Animal
- Bioinformatics
- Plant
- MinION
- P2
September 17 2024
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needLR: a structural variant filtering and prioritization tool for long-read sequencing data
- Whole genome
- Bioinformatics
- Human genomics
- PromethION
- Assembly
- SNVs
September 17 2024