Resource Centre
554 results
Workflow: tumour-normal sequencing
- Workflow
- Structural variation
- SNVs
- Epigenetics
- Methylation
- Cancer research
- Human genomics
- Whole genome
- PromethION
- Kits
- Sample prep
- Variant calling
August 4 2023
Workflow: structural variation
- Structural variation
- PromethION
- Human genomics
- Library prep
- Bioinformatics
- Alignment
- Variant calling
- gDNA
- Clinical research
- Workflow
November 10 2023
Workflow: large cohort sequencing
- Workflow
- Human genomics
- Clinical research
- Population genomics
- Whole genome
- Structural variation
- Variant calling
- Assembly
- Sample prep
- Library prep
- Methylation
- SNVs
October 12 2023
Workflow: human variant calling
- Human genomics
- Clinical research
- Cancer research
- PromethION
- Whole genome
- Variant calling
- Epigenetics
- Phasing
- Methylation
- Structural variation
- SNVs
July 5 2024
William Jeck: Nanopore sequencing and rapid fusion testing – a ‘killer app’ in molecular pathology
- Nanopore Community Meeting
- Oncology
- Structural variation
December 14 2018
The whole is greater than the sum of its parts: long-read sequencing for solving clinical problems in haematology
- Cancer research
- Structural variation
- Targeted
January 23 2024
Whole-genome sequencing of rare disease patients in a national healthcare system
- Human genomics
- Clinical research
- Whole genome
- DNA
- gDNA
- Structural variation
- Variant calling
- Long-read
February 18 2020
Whole-genome sequencing with long reads reveals complex structure and origin of structural variation in human genetic variations and somatic mutations in cancer
- Long-read
- Whole genome
- Human genomics
- Cancer research
- Oncology
- SNVs
- Structural variation
- Variant calling
- MinION
April 29 2021
Whole-genome sequencing in disease samples with haplotype resolved and annotated genetic variation
- Clinical research
- PromethION
- gDNA
- Whole genome
- Variant calling
- Structural variation
- SNVs
- Methylation
May 15 2023
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
Webinar: Structural variants in the French-Canadian population
- Structural variation
- Human genomics
October 30 2020
Webinar - Nanopore from 100 to 1000 genomes: towards a better understanding of phenotypes
- Structural variation
- Human genomics
- Assembly
- Bioinformatics
- Webinar
January 10 2020
Vulcan: Improved long-read mapping and structural variant calling via dual-mode alignment
- Long-read
- Bioinformatics
- Structural variation
- Variant calling
- Alignment
September 24 2021
Virus-derived variation in diverse human genomes
- Microbiology
- Virus
- Targeted
- Structural variation
- Human genomics
- Flongle
- DNA
- Amplicons
- Evolution
November 20 2020
Virtual Nanopore Day, Australia - Rare Disease and Neurology
- Neuroscience
- Structural variation
February 11 2021
Virtual Nanopore Day, Edinburgh
- Infectious disease
- Virus
- Outbreak
- GridION
- MinION
- Bioinformatics
- Direct analysis
- RNA
- cDNA
- Long-read
- Structural variation
November 25 2020
Cloud computing for clinical nanopore fusion detection
- Cancer research
- Clinical research
- Structural variation
September 8 2021
Variants at the ASIP locus contribute to coat color darkening in Nellore cattle
- Long-read
- Structural variation
- MinION
- gDNA
- DNA
- Whole genome
- Animal
April 28 2021
VACmap: an accurate long-read aligner for unravelling complex genomic rearrangements
- Bioinformatics
- Structural variation
- Human genomics
May 7 2024
Using Targeted Nanopore Technologies
- DNA
- Targeted
- Phasing
- Structural variation
- SNVs
- Clinical research
January 27 2021