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Events and webinars


BioTechX
Upcoming

BioTechX

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ACGS Summer Scientific Meeting 2023
Upcoming

ACGS Summer Scientific Meeting 2023

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European Human Genetics Conference - ESHG 2023
Upcoming

European Human Genetics Conference - ESHG 2023

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From Research to Transforming Patients’ Lives
Upcoming

From Research to Transforming Patients’ Lives

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Genomic Sequencing to Improve Cancer Care
On-Demand

Genomic Sequencing to Improve Cancer Care

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Transforming Cancer Care Using Genomic Tests
On-Demand

Transforming Cancer Care Using Genomic Tests

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Deciphering Developmental Disorders
On-Demand

Deciphering Developmental Disorders

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The Real Costs of Rare Disease
On-Demand

The Real Costs of Rare Disease

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Priorisation des variants entièrement interprétable basée sur l’Intelligence Artificielle Fournit des résultats rapides et exploitables pour les patients
On-Demand

Priorisation des variants entièrement interprétable basée sur l’Intelligence Artificielle Fournit des résultats rapides et exploitables pour les patients

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Prenatal Diagnosis in the Era of Genomic Medicine
On-Demand

Prenatal Diagnosis in the Era of Genomic Medicine

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Prenatal Diagnosis with Congenica
On-Demand

Prenatal Diagnosis with Congenica

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Improving Rare Disease Diagnosis in the 100,000 Genomes Project (UK 100K)
On-Demand

Improving Rare Disease Diagnosis in the 100,000 Genomes Project (UK 100K)

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Genomics in Medicine: Working with National Genome Programmes
On-Demand

Genomics in Medicine: Working with National Genome Programmes

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Why choose a professional solution?
On-Demand

Why choose a professional solution?

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Latest developments in next-generation genomic data analysis
On-Demand

Latest developments in next-generation genomic data analysis

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Prenatal diagnosis using Whole Exome Sequencing (WES)
On-Demand

Prenatal diagnosis using Whole Exome Sequencing (WES)

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From bench to bedside: Best practices in diagnosing and treating pediatric patients with epilepsy
On-Demand

From bench to bedside: Best practices in diagnosing and treating pediatric patients with epilepsy

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Chris Wigley, CEO Genomics England: To Infinity and Beyond – working together to bring genomic medicine to EVERYONE
On-Demand

Chris Wigley, CEO Genomics England: To Infinity and Beyond – working together to bring genomic medicine to EVERYONE

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Richard Durbin: Long-read sequencing and new reference genomes
On-Demand

Richard Durbin: Long-read sequencing and new reference genomes

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Precision therapies in the epilepsies
On-Demand

Precision therapies in the epilepsies

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Polygenic Risk Scores & the Future of Precision Medicine: Challenges and Opportunities
On-Demand

Polygenic Risk Scores & the Future of Precision Medicine: Challenges and Opportunities

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The Genetics of COVID-19
On-Demand

The Genetics of COVID-19

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Accelerating the Identification of Genetic Diseases
On-Demand

Accelerating the Identification of Genetic Diseases

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Prenatal exome analysis – finding the molecular cause of fetal anomalies, faster
On-Demand

Prenatal exome analysis – finding the molecular cause of fetal anomalies, faster

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Increasing case throughput: How to gain immediate insight into clinically relevant evidence
On-Demand

Increasing case throughput: How to gain immediate insight into clinically relevant evidence

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Phenotype-based prioritisation of variants with Exomiser
On-Demand

Phenotype-based prioritisation of variants with Exomiser

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Clinically relevant CNV detection via WGS and ExomeCG WES – towards a single assay approach
On-Demand

Clinically relevant CNV detection via WGS and ExomeCG WES – towards a single assay approach

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Influencing prenatal clinical management using exome sequencing
On-Demand

Influencing prenatal clinical management using exome sequencing

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Faster Analysis of Neurodevelopmental Disorders with Congenica Neuro
On-Demand

Faster Analysis of Neurodevelopmental Disorders with Congenica Neuro

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Real-World Examples of Efficiency Gains in the Analysis & Interpretation of Genomic Data
On-Demand

Real-World Examples of Efficiency Gains in the Analysis & Interpretation of Genomic Data

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Achieving a Definitive Diagnosis for Epilepsy Patients
On-Demand

Achieving a Definitive Diagnosis for Epilepsy Patients

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Discovering the Missing Link between my Rare Disease and an Olympic Athlete
On-Demand

Discovering the Missing Link between my Rare Disease and an Olympic Athlete

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Rare Inherited Disease: 30 Min from data to report
On-Demand

Rare Inherited Disease: 30 Min from data to report

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Practical Applications of Genome Interpretation for Rare Disease Diagnosis and Research
On-Demand

Practical Applications of Genome Interpretation for Rare Disease Diagnosis and Research

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