Clinical Sequencing Evidence-Generating Research (CSER) - Gail Jarvik and Kyle Brothers
Hypothesis-Generating Research and Predictive Medicine
Variant interpretation: from the clinic to the lab… and back again
Evidence Generation for Genomic Medicine (Summary) - Sharon Plon
Oncology Outcomes | Real-World Data Evidence Generation & Presentation
CSER2 Pre-Application Informational Webinar - Lucia Hindorff
Facilitating Development of a Shared Evidence Base for Healthcare Systems (Challenges) - Heidi Rehm
My Research Results
Translational Science in Drug Development: Surrogate Endpoints, Biomarkers, and More - Day 1
Evidence Generation for Genomic Medicine (eMERGE) - Marc Williams
Overcoming Challenges of CNV and Sequence Variant Interpretation in the Clinical Lab
The Use of Next-Generation Sequencing in Drug Development
Identify Genes based on EST Evidence
Panel 1: Key Unaddressed Evidence Gaps in Implementing Genomic Medicine
Evidence Generation for Genomic Medicine (Discussion)
E08.1 - Using genomic resources to interpret the clinical significance of rare variants
Bold Predictions for Human Genomics by 2030: Session 7
Aggregating and Sharing Clinical Evidence to Improve the Diagnosis of Rare Diseases
Translating sequencing into clinical practice in Africa: a health economics perspective
Variant Interpretation Challenges & Use Cases | Leveraging Mastermind in the Clinical Lab
Integrating Genomic Data to Enhance Neurobiology Discovery
Mastermind Genomic Intelligence Platform: Curated Evidence and Article Viewer
Develop Comprehensive Health Records with Pharmacogenomics
Seminars in Genomic Medicine: Dr Heidi Rehm
Head Start: The Promise of Universal Newborn Sequencing
