Resource Centre
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Workflow overview: tumour-normal sequencing
- SNVs
- Workflow
- Structural variation
- Epigenetics
- Methylation
- Cancer research
August 4 2023
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Workflow overview: large cohort sequencing
- SNVs
- Workflow
- Human genomics
- Clinical research
- Population genomics
- Whole genome
October 12 2023
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Workflow overview: human variant calling
- SNVs
- Human genomics
- Clinical research
- Cancer research
- PromethION 24/48
- Whole genome
April 29 2025
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Whole-genome sequencing of SARS-CoV-2 in the Republic of Ireland during waves 1 and 2 of the pandemic
- SNVs
- MinION
- GridION
- Microbiology
- Outbreak
- cDNA
February 10 2021
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Whole-genome sequencing with long reads reveals complex structure and origin of structural variation in human genetic variations and somatic mutations in cancer
- SNVs
- Long-read
- Whole genome
- Human genomics
- Cancer research
- Oncology
April 29 2021
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Whole-genome sequencing in disease samples with haplotype resolved and annotated genetic variation
- SNVs
- Clinical research
- PromethION
- gDNA
- Whole genome
- Variant calling
May 15 2023
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Whole genome sequencing and phylogenetic classification of Tunisian SARS-CoV-2 strains from patients of the Military Hospital in Tunis
- SNVs
- Microbiology
- Infectious disease
- Virus
- Outbreak
- GridION
October 9 2020
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Whole-genome insights: nanopore sequencing in neuropathology
- SNVs
- SNVs
- PromethION 2
- PromethION 24/48
- EPI2ME
- Epigenetics
May 19 2025
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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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Viral sequencing reveals US healthcare personnel rarely become infected with SARS-CoV-2 through patient contact
- SNVs
- GridION
- Microbiology
- Outbreak
- cDNA
- RNA
February 1 2021
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Viral genetic sequencing identifies staff transmission of COVID-19 is important in a community hospital outbreak
- SNVs
- MinION
- Microbiology
- Outbreak
- cDNA
- RNA
February 19 2021
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Validation of a comprehensive long-read sequencing platform for broad clinical genetic diagnosis
- SNVs
- Human genomics
- Bioinformatics
- Clinical research
- Structural variation
- PromethION 24/48
May 2 2025
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Utilizing nanopore sequencing technology for the rapid and comprehensive characterization of eleven HLA loci
- SNVs
- Human genomics
- Phasing
- DNA
- Amplicons
- Targeted
June 25 2020
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Using Targeted Nanopore Technologies
- SNVs
- DNA
- Targeted
- Phasing
- Structural variation
- Clinical research
January 27 2021
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Using long-read nanopore sequencing to unravel structural genomic variations in plants
- SNVs
- London Calling
- Plant
- gDNA
- MinION
May 29 2019
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Unprecedented access to haplotype-resolved biology enabled by ultra-long reads and Pore-C
- SNVs
- Phasing
- 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
- SNVs
- Phasing
- Plant
- Structural variation
- Targeted
- London Calling
May 19 2023
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Unique mutational changes in SARS-CoV2 genome of different state of India
- SNVs
- Microbiology
- Infectious disease
- Virus
- Outbreak
- RNA
August 25 2020
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Unique K-mer sequences for validating cancer-related substitution, insertion and deletion mutations
- SNVs
- Whole genome
- Variant calling
- gDNA
- DNA
- Bioinformatics
June 20 2020
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Ultra-rich human data — variant analysis with EPI2ME
- SNVs
- Bioinformatics
- Human genomics
- Population genomics
- EPI2ME
- Epigenetics
September 17 2024