Resource Centre
185 results
ZCWPW1 loss-of-function variants in Alzheimer’s Disease
- Long-read
- Phasing
- Variant calling
- Human genomics
- Clinical research
- Targeted
- MinION
August 13 2021
Workflow: human variant calling
- Human genomics
- Clinical research
- Cancer research
- PromethION
- Whole genome
- Variant calling
- Epigenetics
- Phasing
- Methylation
- Structural variation
- SNVs
July 5 2024
Parent-of-origin-aware genomic analysis infers segregation of pathogenic variants
- Cancer research
- Clinical research
- Human genomics
- Phasing
- Methylation
- Epigenetics
June 26 2023
Variant segregation in rare disease singletons and duos using nanopore adaptive sampling
- Bioinformatics
- Clinical research
- Phasing
- Targeted
- MinION
- Nanopore Community Meeting
September 27 2023
Utilizing nanopore sequencing technology for the rapid and comprehensive characterization of eleven HLA loci; addressing the need for deceased donor expedited HLA typing
- Human genomics
- SNVs
- Phasing
- DNA
- Amplicons
- Targeted
- MinION
- Clinical research
- Variant calling
- Flongle
June 25 2020
Using Targeted Nanopore Technologies
- DNA
- Targeted
- Phasing
- Structural variation
- SNVs
- Clinical research
January 27 2021
Using Oxford Nanopore sequencing in grapevine breeding
- London Calling
- Plant
- Bioinformatics
- Phasing
- Epigenetics
- MinION
- GridION
- PromethION
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
- Plant
- Population genomics
- Variant calling
- Phasing
- Assembly
- Bioinformatics
- PromethION
- Q20+
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
Understanding the drivers of oncogenesis
- PromethION
- London Calling
- Long-read
- Cancer research
- Structural variation
- Phasing
September 14 2023
Ultra-rich human data — variant analysis with EPI2ME
- Bioinformatics
- Human genomics
- Population genomics
- EPI2ME
- Epigenetics
- SNVs
- Phasing
- Structural variation
- Whole genome
September 17 2024
Transforming cancer care: redefining cancer characterization and predisposition insights through nanopore sequencing
- Cancer research
- Human genomics
- MinION
- Flongle
- Epigenetics
- SNVs
- Phasing
- Structural variation
- Targeted
September 17 2024
Targeted sequencing of the entire blood group genome by adaptive sampling
- Phasing
- Variant calling
- Immunology
- London Calling
May 24 2024
Targeted adaptive long-read sequencing for discovery of complex phased variants in inherited retinal disease patients
- Targeted
- Long-read
- Phasing
- Variant calling
- Structural variation
- SNVs
- Real-time
May 26 2023
The structure, function, and evolution of a complete human chromosome 8
- Whole genome
- Assembly
- Long-read
- gDNA
- DNA
- PromethION
- Methylation
- Epigenetics
- Human genomics
- Phasing
April 7 2021
Structural variation in All of Us analyzed with long-read sequencing at a scale
- Nanopore Community
- Human genomics
- Population genomics
- SNVs
- Phasing
- Long-read
- Whole genome
- Nanopore Community Meeting
December 11 2023
Workflow: SNV calling and phasing
- Human genomics
- Whole genome
- Workflow
- SNVs
- Structural variation
- Phasing
September 19 2022
Single-molecule simultaneous profiling of DNA methylation and DNA–protein interactions with Nanopore-DamID
- Bioinformatics
- Epigenetics
- SNVs
- Phasing
- Whole genome
- MinION
May 28 2022
Simultaneous de novo calling and phasing of genetic variants at chromosome-scale using NanoStrand-seq
- Phasing
- Human genomics
- PromethION
July 9 2024