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918 results

Human genomics

Publication
ZCWPW1 loss-of-function variants in Alzheimer’s Disease
August 13 2021
Workflow
Workflow overview: tumour-normal sequencing
July 21 2025
Workflow
Workflow overview: single-cell transcriptomics
February 24 2025
Workflow
Workflow overview: 24-hour human whole-genome sequencing
September 17 2025
Workflow
Workflow overview: pharmacogenomics with adaptive sampling
August 5 2025
Workflow
Workflow overview: large cohort sequencing
July 28 2025
Workflow
Workflow overview: human variant calling
April 29 2025
Workflow
Workflow overview: direct RNA sequencing
September 8 2025
Bioinformatics tool
Whole Human Genome Sequencing Project
June 20 2019
Publication
Whole human genome 5'-mC methylation analysis using long read nanopore sequencing
May 21 2021
Publication
Whole-genome sequencing of rare disease patients in a national healthcare system
February 18 2020
Publication
Whole-genome sequencing with long reads reveals complex structure and origin of structural variation in human genetic variations and somatic mutations in cancer
April 29 2021
Bioinformatics tool
Wengan: Efficient and high quality hybrid de novo assembly of human genomes
November 25 2019
Publication
Webinar: Structural variants in the French-Canadian population
October 30 2020
Video
Webinar in Spanish: Aumento potencial del rendimiento diagnóstico en genómica humana, gracias a la secuenciación por nanoporos
September 1 2023
Video
Scalable nanopore sequencing for Alzheimer’s research
May 3 2023
Video
Parent-of-origin-aware genomic analysis infers segregation of pathogenic variants
June 26 2023
Video
Webinar - Nanopore from 100 to 1000 genomes: towards a better understanding of phenotypes
January 10 2020
Video
Integrating 10x Genomics single-cell and spatial profiling with Oxford Nanopore long-read sequencing
January 19 2024
Video
Human genome sequencing on PromethION webinar
October 11 2018

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Resource Centre

ZCWPW1 loss-of-function variants in Alzheimer’s Disease

Workflow overview: tumour-normal sequencing

Workflow overview: single-cell transcriptomics

Workflow overview: 24-hour human whole-genome sequencing

Workflow overview: pharmacogenomics with adaptive sampling

Workflow overview: large cohort sequencing

Workflow overview: human variant calling

Workflow overview: direct RNA sequencing

Whole Human Genome Sequencing Project

Whole human genome 5'-mC methylation analysis using long read nanopore sequencing

Whole-genome sequencing of rare disease patients in a national healthcare system

Whole-genome sequencing with long reads reveals complex structure and origin of structural variation in human genetic variations and somatic mutations in cancer

Wengan: Efficient and high quality hybrid de novo assembly of human genomes

Webinar: Structural variants in the French-Canadian population

Webinar in Spanish: Aumento potencial del rendimiento diagnóstico en genómica humana, gracias a la secuenciación por nanoporos

Scalable nanopore sequencing for Alzheimer’s research

Parent-of-origin-aware genomic analysis infers segregation of pathogenic variants

Webinar - Nanopore from 100 to 1000 genomes: towards a better understanding of phenotypes

Integrating 10x Genomics single-cell and spatial profiling with Oxford Nanopore long-read sequencing

Human genome sequencing on PromethION webinar

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