Resource Centre
Publication )
ZCWPW1 loss-of-function variants in Alzheimer’s Disease
Workflow )
Workflow overview: tumour-normal sequencing
Workflow )
Workflow overview: single-cell transcriptomics
Workflow )
Workflow overview: 24-hour human whole-genome sequencing
Workflow )
Workflow overview: pharmacogenomics with adaptive sampling
Workflow )
Workflow overview: large cohort sequencing
Workflow )
Workflow overview: human variant calling
Workflow )
Workflow overview: direct RNA sequencing
Bioinformatics tool )
Whole Human Genome Sequencing Project
Publication )
Whole human genome 5'-mC methylation analysis using long read nanopore sequencing
Publication )
Whole-genome sequencing of rare disease patients in a national healthcare system
Publication )
Whole-genome sequencing with long reads reveals complex structure and origin of structural variation in human genetic variations and somatic mutations in cancer
Bioinformatics tool )
Wengan: Efficient and high quality hybrid de novo assembly of human genomes
Events )
Webinar: Structural variants in the French-Canadian population
Video )
Webinar in Spanish: Aumento potencial del rendimiento diagnóstico en genómica humana, gracias a la secuenciación por nanoporos
Video )
Scalable nanopore sequencing for Alzheimer’s research
Video )
Parent-of-origin-aware genomic analysis infers segregation of pathogenic variants
Video )
Webinar - Nanopore from 100 to 1000 genomes: towards a better understanding of phenotypes
Video )
Integrating 10x Genomics single-cell and spatial profiling with Oxford Nanopore long-read sequencing
Video )
Human genome sequencing on PromethION webinar
