Resource Centre
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Whole-genome sequencing in disease samples with haplotype resolved and annotated genetic variation
- Clinical research
- PromethION
- gDNA
- Whole genome
- Variant calling
- Structural variation
May 15 2023
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Whole genome Nanopore DNA analysis shows that chronic corticosterone supplementation results in altered sperm DNA methylation.
- London Calling
- Animal
- Bioinformatics
- Whole genome
May 19 2023
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Whole-genome DNA sequencing using nanopore R10.4 promises best practice for single-cell variation detection and methylation profiling
- SNVs
- Structural variation
- Whole genome
- London Calling
May 19 2023
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Whole-genome analysis of VREfm isolates with daptomycin resistance using Oxford Nanopore and Illumina sequencing
- Bioinformatics
- Whole genome
- Clinical research
- Infectious disease
- Bacteria
- Microbiology
June 20 2019
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Validation and application of multiplex nanopore MinION sequencing for molecular typing of human adenoviruses in clinical samples: a cost effective sequencing strategy
- Virus
- Microbiology
- MinION
- Clinical research
- Infectious disease
- Amplicons
April 29 2019
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Validation and quality control of a molecular cloning experiment using de novo assembly of Oxford Nanopore reads
- London Calling
- EPI2ME
- Plasmid
May 20 2025
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Unprecedented access to haplotype-resolved biology enabled by ultra-long reads and Pore-C
- Phasing
- SNVs
- Long-read
- PromethION
- Methylation
- Chromatin conformation
May 15 2023
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Unlocking the power of haplotype-based molecular breeding using long read DNA sequencing
- Phasing
- Plant
- SNVs
- Structural variation
- Targeted
- London Calling
May 19 2023
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Unlocking Nanopore sequencing for managing food safety in the food industry
- London Calling
- Bioinformatics
- Infectious disease
- Microbiology
- Whole genome
May 19 2023
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Universal, amplicon-based sequencing method for Canine Morbillivirus (CDV)
- Microbiology
- Whole genome
- MinION
May 28 2022
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Understanding genetic variation in cancer using targeted long-read sequencing
- Cancer research
- Targeted
- Structural variation
- Long-read
- Human genomics
September 26 2019
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Uncovering the full-length extracellular transcriptome in human blood plasma using long-read cDNA sequencing
- Cancer research
- Gene expression
- Transcriptome
May 28 2022
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Ultra-long reads and ultra-long duplications: What nanopore sequencing is revealing about Bordetella pertussis
- Microbiology
- Bacteria
- Long-read
- MinION
- Whole genome
- gDNA
May 17 2019
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Ultra-fast deep-learned pediatric CNS tumor classification during surgery
- London Calling
- Cancer research
- Clinical research
- Epigenetics
May 19 2023
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Ultra-fast and cost-effective pathogen identification and resistance gene detection in a clinical research setting using nanopore Flongle sequencing
- Bioinformatics
- Infectious disease
- Metagenomics
- Microbiology
- Whole genome
- Flongle
May 28 2022
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Transcriptome-wide expression and RNA modifications with full-length native RNA and cDNA sequencing
- London Calling
- cDNA
- RNA
- Transcriptomics
May 20 2025
