Genetics and genomics research now includes approaches that integrate laboratory data with electronic medical record (EMR) systems for genomic discovery and implementing genomic medicine in the clinic. These avenues are being addressed through multiple initiatives around the world. This year's HGVS meeting will present speakers who represent several ongoing projects focused on leveraging the EMR to help interpret genetic variation, highlighting bench-to-bedside and bedside-to-bench approaches.
Organized by:
Human Genome Variation Society
Invited Speakers:
CSER (Clinical Sequencing Exploratory Research) Initiative - Brian Shirts
Informatics & Phenotype - Marylyn Ritchie
Fast Healthcare Interoperability Resource - Atul Butte
Topic TBA - Melissa Haendel
EHR and Genomics to Find Mendelian Disease - Josh Denny*