Katherine Dixon - Characterising structural variants in rare disease
Katherine Dixon - Characterising structural variants in rare disease
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Katherine Dixon - Characterising structural variants in rare disease

Katherine Dixon - Characterising structural variants in rare disease

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Katherine Dixon: Clinical and functional significance of germline variation in cancer susceptibi...

Katherine Dixon: Clinical and functional significance of germline variation in cancer susceptibi...

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The long and short of structural variants using Oxford Nanopore sequencing

The long and short of structural variants using Oxford Nanopore sequencing

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Nanopore Sequencing Identified Structural Variants in the French Canadian population - Sarah Reiling

Nanopore Sequencing Identified Structural Variants in the French Canadian population - Sarah Reiling

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Sequencing, Variant Calling, and Cancer Genomics

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Toward a Definitive Standard of Germline Structural Variants using Multiple Genomic Technologies

Toward a Definitive Standard of Germline Structural Variants using Multiple Genomic Technologies

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Fritz Sedlazeck: Rapid structural variant calling across AllOfUs using Oxford Nanopore sequencing

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The Challenges of Diagnosing Rare Diseases

The Challenges of Diagnosing Rare Diseases

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Genome sequencing of thousands of patients with rare blood disorders

Genome sequencing of thousands of patients with rare blood disorders

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Kishwar Shafin - Accurate variant calling and de novo assembly with nanopore reads

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Blood donor genotyping - how can long range sequencing help? | Nicholas Gleadall

Blood donor genotyping - how can long range sequencing help? | Nicholas Gleadall

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Mary Dixon Woods - Measuring What Matters

Mary Dixon Woods - Measuring What Matters

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Sophie Teullet - What can we learn from pangolins' penchant for ants?

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