Resource Centre
788 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: 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: single-cell transcriptomics
- Single cell
- Transcriptome
- PromethION
- Cancer research
- Clinical research
- cDNA
- Workflow
- Human genomics
- Splice variation
- Gene fusions
- Gene expression
- Kits
February 20 2024
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
Workflow: direct RNA sequencing
- Workflow
- RNA
- cDNA
- Methylation
- Epigenetics
- Human genomics
- Clinical research
- Isoforms
- Splice variation
- Transcriptome
February 26 2024
Workflow: Characterising structural variants in FFPE cancer research samples
- Workflow
- Cancer research
- Clinical research
- Whole genome
- Human genomics
- Sample prep
- Library prep
- gDNA
- DNA
- PromethION
- Bioinformatics
July 8 2022
Whole Human Genome Sequencing Project
- Bioinformatics
- Human genomics
- Whole genome
- Assembly
- MinION
- gDNA
June 20 2019
Whole human genome 5'-mC methylation analysis using long read nanopore sequencing
- Whole genome
- Human genomics
- Methylation
- Epigenetics
- DNA
- gDNA
- MinION
May 21 2021
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
White paper: advantages of long reads for genome assembly
- Whole genome
- Human genomics
- Plant
- Microbiology
- Assembly
- Animal
September 7 2021
Wengan: Efficient and high quality hybrid de novo assembly of human genomes
- Assembly
- DNA
- gDNA
- Whole genome
- Human genomics
- Bioinformatics
November 25 2019
Webinar: Structural variants in the French-Canadian population
- Structural variation
- Human genomics
October 30 2020
Scalable nanopore sequencing for Alzheimer’s research
- Human genomics
- Neuroscience
- Population genomics
May 3 2023
Parent-of-origin-aware genomic analysis infers segregation of pathogenic variants
- Cancer research
- Clinical research
- Human genomics
- Phasing
- Methylation
- Epigenetics
June 26 2023
Webinar - Nanopore from 100 to 1000 genomes: towards a better understanding of phenotypes
- Structural variation
- Human genomics
- Assembly
- Bioinformatics
- Webinar
January 10 2020
Integrating 10x Genomics single-cell and spatial profiling with Oxford Nanopore long-read sequencing
- Single cell
- Webinar
- Human genomics
January 19 2024