Resource Centre
ZCWPW1 loss-of-function variants in Alzheimer’s Disease
- Phasing
 - Long-read
 - Variant calling
 - Human genomics
 - Clinical research
 - Targeted
 
August 13 2021
Workflow overview: pharmacogenomics with adaptive sampling
- Phasing
 - Pharmacogenomics
 - Biopharma
 - Human genomics
 - Clinical research
 - Targeted
 
August 5 2025
Workflow overview: human variant calling
- Phasing
 - Human genomics
 - Clinical research
 - Cancer research
 - PromethION 24/48
 - Whole genome
 
April 29 2025
Parent-of-origin-aware genomic analysis infers segregation of pathogenic variants
- Phasing
 - Cancer research
 - Clinical research
 - Human genomics
 - Methylation
 - Epigenetics
 
June 26 2023
Verkko2: integrating proximity ligation data with long-read De Bruijn graphs for efficient telomere-to-telomere genome assembly, phasing, and scaffold
- Phasing
 - Bioinformatics
 - Long-read
 
December 26 2024
Variant segregation in rare disease singletons and duos using nanopore adaptive sampling
- Phasing
 - Bioinformatics
 - Clinical research
 - Targeted
 - MinION
 - Nanopore Community Meeting
 
September 27 2023
Variant phasing for antisense oligonucleotide design using adaptive sampling
- Phasing
 - Phasing
 - PromethION 24/48
 - Targeted
 - Human genomics
 - PromethION 24/48
 
May 19 2025
Utilizing nanopore sequencing technology for the rapid and comprehensive characterization of eleven HLA loci
- Phasing
 - Human genomics
 - SNVs
 - DNA
 - Amplicons
 - Targeted
 
June 25 2020
Using ultra-long-read Oxford Nanopore sequencing to detect complex structural variants in leukaemia
- Phasing
 - Phasing
 - MinION
 - PromethION 2
 - Structural variation
 - Targeted
 
May 19 2025
Using Targeted Nanopore Technologies
- Phasing
 - DNA
 - Targeted
 - Structural variation
 - SNVs
 - Clinical research
 
January 27 2021
Using Oxford Nanopore sequencing in grapevine breeding
- Phasing
 - London Calling
 - Plant
 - Bioinformatics
 - Epigenetics
 - MinION
 
May 24 2024
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
Unlocking the banana pangenome: harnessing genetic diversity
- Phasing
 - Plant
 - Population genomics
 - Variant calling
 - Assembly
 - Bioinformatics
 
May 24 2024
Unlocking the power of haplotype-based molecular breeding using long read DNA sequencing
- Phasing
 - Plant
 - SNVs
 - Structural variation
 - Targeted
 - London Calling
 
May 19 2023
Case study: understanding the drivers of oncogenesis
- Phasing
 - PromethION
 - London Calling
 - Long-read
 - Cancer research
 - Structural variation
 
September 14 2023
Ultrarapid and high-resolution HLA class I typing using transposase-based nanopore sequencing applied in pharmacogenetic testing
- Phasing
 - Human genomics
 - Clinical research
 - Targeted
 - Amplicons
 - MinION
 
June 23 2023
Ultra-rich human data — variant analysis with EPI2ME
- Phasing
 - Bioinformatics
 - Human genomics
 - Population genomics
 - EPI2ME
 - Epigenetics
 
September 17 2024
Ultra-long sequencing for contiguous haplotype resolution of the human immunoglobulin heavy chain locus
- Phasing
 - Human genomics
 - Long-read
 - Adaptive sampling
 - Structural variation
 - PromethION
 
December 17 2024
Transforming cancer care: redefining cancer characterization and predisposition insights through nanopore sequencing
- Phasing
 - Cancer research
 - Human genomics
 - MinION
 - Flongle
 - Epigenetics
 
September 17 2024
The utility of long-read sequencing in diagnosing early-onset Parkinson's disease
- Phasing
 - Human genomics
 - Neuroscience
 - Structural variation
 - Adaptive sampling
 - PromethION
 
December 19 2024
)
)
)
)
)
)
)
)
)
)
)
)
)
)
)
)
)
)
)