The potential clinical utility of amplicon and targeted nanopore sequencing for rare disease

The potential clinical utility of amplicon and targeted nanopore sequencing for rare disease

Nanopore sequencing as a potential diagnostic tool for genetic diseases in the Middle EastПодробнее

Nanopore sequencing as a potential diagnostic tool for genetic diseases in the Middle East

Potential use of nanopore sequencing in clinical cancer genomicsПодробнее

Potential use of nanopore sequencing in clinical cancer genomics

Nanopore sequencing reveals retrotransposon insertions or complex genetic mechanisms rare disordersПодробнее

Nanopore sequencing reveals retrotransposon insertions or complex genetic mechanisms rare disorders

Uncovering rare disease-causing variantsПодробнее

Uncovering rare disease-causing variants

Amplicons to whole genomes: clinical sequencing using nanopore technology | Andrew BeggsПодробнее

Amplicons to whole genomes: clinical sequencing using nanopore technology | Andrew Beggs

Long-read sequencing for pathogenic and novel variation discovery in rare diseasesПодробнее

Long-read sequencing for pathogenic and novel variation discovery in rare diseases

Maximizing the power of genomic sequencing in pediatric rare diseaseПодробнее

Maximizing the power of genomic sequencing in pediatric rare disease

Levin Joe Klages: Analysis of clinical research samples by nanopore sequencingПодробнее

Levin Joe Klages: Analysis of clinical research samples by nanopore sequencing

Efficient targeted sequencing using nanopore sequencingПодробнее

Efficient targeted sequencing using nanopore sequencing

Solving genetically undiagnosed inherited neuropathy families: long-read sequencing to the rescueПодробнее

Solving genetically undiagnosed inherited neuropathy families: long-read sequencing to the rescue

Improved detection and clinical interpretation of rare disease variantsПодробнее

Improved detection and clinical interpretation of rare disease variants

Team Pitches – UnifAIПодробнее

Team Pitches – UnifAI

PromethION - flexible, scalable, on-demand sequencingПодробнее

PromethION - flexible, scalable, on-demand sequencing

Genomic Sequencing Advancements Provide Answers to Rare Diseases | Summer's StoryПодробнее

Genomic Sequencing Advancements Provide Answers to Rare Diseases | Summer's Story

Ryan McGinty | Lightning TalkПодробнее

Ryan McGinty | Lightning Talk

Katherine Dixon - Characterising structural variants in rare diseaseПодробнее

Katherine Dixon - Characterising structural variants in rare disease

The potential use of nanopore sequencing for molecular diagnosis of germline cancer predispositionПодробнее

The potential use of nanopore sequencing for molecular diagnosis of germline cancer predisposition

Ron Ammar | Nanopore Sequencing for Detection of Pharmacogenomic Variants and HaplotypesПодробнее

Ron Ammar | Nanopore Sequencing for Detection of Pharmacogenomic Variants and Haplotypes