Login
Please select your location and reference genome:
America - GRCh37 America - GRCh38 Europe, Middle East, Africa - GRCh37 Europe, Middle East, Africa - GRCh38

Events and webinars


RareSummit23
Upcoming

RareSummit23

View Event
International Conference on Newborn Sequencing (ICONS)
Upcoming

International Conference on Newborn Sequencing (ICONS)

View Event
BioTechX
Upcoming

BioTechX

View Event
ESHG 2023 Satellite Symposium
On-Demand

ESHG 2023 Satellite Symposium

View Event
From Research to Transforming Patients’ Lives
On-Demand

From Research to Transforming Patients’ Lives

View Event
Deciphering Developmental Disorders - celebrating 10 years of innovation
On-Demand

Deciphering Developmental Disorders - celebrating 10 years of innovation

View Event
Driving Precision Medicine at Scale
On-Demand

Driving Precision Medicine at Scale

View Event
Ending the Diagnostic Odyssey - where next?
On-Demand

Ending the Diagnostic Odyssey - where next?

View Event
Transforming Lives through Healthcare
On-Demand

Transforming Lives through Healthcare

View Event
From 1000 Genomes to UK10K: The power and challenges of large-scale national programs
On-Demand

From 1000 Genomes to UK10K: The power and challenges of large-scale national programs

View Event
Genomic Sequencing to Improve Cancer Care
On-Demand

Genomic Sequencing to Improve Cancer Care

View Event
Transforming Cancer Care Using Genomic Tests
On-Demand

Transforming Cancer Care Using Genomic Tests

View Event
Deciphering Developmental Disorders
On-Demand

Deciphering Developmental Disorders

View Event
The Real Costs of Rare Disease
On-Demand

The Real Costs of Rare Disease

View Event
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

View Event
Prenatal Diagnosis in the Era of Genomic Medicine
On-Demand

Prenatal Diagnosis in the Era of Genomic Medicine

View Event
Prenatal Diagnosis with Congenica
On-Demand

Prenatal Diagnosis with Congenica

View Event
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)

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

Genomics in Medicine: Working with National Genome Programmes

View Event
Why choose a professional solution?
On-Demand

Why choose a professional solution?

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

Latest developments in next-generation genomic data analysis

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

Prenatal diagnosis using Whole Exome Sequencing (WES)

View Event
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

View Event
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

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

Richard Durbin: Long-read sequencing and new reference genomes

View Event
Precision therapies in the epilepsies
On-Demand

Precision therapies in the epilepsies

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

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

View Event
The Genetics of COVID-19
On-Demand

The Genetics of COVID-19

View Event
Accelerating the Identification of Genetic Diseases
On-Demand

Accelerating the Identification of Genetic Diseases

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

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

View Event
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

View Event
Phenotype-based prioritisation of variants with Exomiser
On-Demand

Phenotype-based prioritisation of variants with Exomiser

View Event
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

View Event
Influencing prenatal clinical management using exome sequencing
On-Demand

Influencing prenatal clinical management using exome sequencing

View Event
Faster Analysis of Neurodevelopmental Disorders with Congenica Neuro
On-Demand

Faster Analysis of Neurodevelopmental Disorders with Congenica Neuro

View Event
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

View Event
Achieving a Definitive Diagnosis for Epilepsy Patients
On-Demand

Achieving a Definitive Diagnosis for Epilepsy Patients

View Event
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

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

Rare Inherited Disease: 30 Min from data to report

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

Practical Applications of Genome Interpretation for Rare Disease Diagnosis and Research

View Event

View Event