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Leveraging the Electronic Medical Record for Genomic Interpretation

 
  July 05, 2018  
     
 


Human Genome Variation Society, San Diego, CA, USA
Tuesday 16 October 2018


Satellite meeting to the American Society of Human Genetics' Annual Meeting.


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*

More topics to be added soon!

(*to be confirmed)

 
Deadline for Abstracts: 31st July 2018
 
Registration: Its all on the website!
E-mail: info@meeting-makers.com
 
   
 
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