Webinar

Webinar: Breaking the Interpretation Bottleneck

2020-06-22T07:54:26+00:00

Webinar: Breaking the interpretation bottleneck Examining the utility of an automated genomic interpretation algorithm in a clinical genetic lab Guest Division Director, Division of Clinical Genomics Interpretation Baylor Genetics Host Chief Science Officer Emedgene The utilization of exome and genome sequencing in clinical practice has become widespread in recent [...]

Webinar: Breaking the Interpretation Bottleneck2020-06-22T07:54:26+00:00

Webinar: Analytical validation of clinical whole genome sequencing

2020-06-22T07:55:45+00:00

#SideByScience Webinar: Analytical validation of clinical whole genome sequencing for germline disease diagnostics: Best practices and performance standards Speaker Co-Director, Centre for Genetic Medicine Associate Director, Department of Paediatric Laboratory Medicine SickKids Dr. Christian Marshall will present the findings of the Medical Genome Initiative, a consortium of leading [...]

Webinar: Analytical validation of clinical whole genome sequencing2020-06-22T07:55:45+00:00

Webinar: Genetics in Epilepsy – Early Steps on the Path to Precision Medicine

2020-06-22T07:56:37+00:00

#SideByScience Webinar Genetics in Epilepsy – Early Steps on the Path to Precision Medicine Annapurna Poduri, MD, MPH Speaker Associate Professor in Neurology, Harvard Medical School Director, Epilepsy Genetics Program Boston Children’s Hospital Date: June 25th, 2020 Time: 12:30PM ET Epilepsy diagnosis and care have changed [...]

Webinar: Genetics in Epilepsy – Early Steps on the Path to Precision Medicine2020-06-22T07:56:37+00:00

test webinar page

2020-06-22T09:10:30+00:00

This webinar presents the work of the Children’s Rare Disease Cohorts (CRDC) initiative at Boston Children’s Hospital, which integrates genomic, research, and clinical data to facilitate hospital-based analysis and reanalysis of genomic data to accelerate rates of discovery and patient diagnoses.

test webinar page2020-06-22T09:10:30+00:00