Day 2 Track 1 Talk: Integrating Genomic Data into Patient Medical Records
We are now over 15 years past the first draft of the human genome, with hundreds of thousands of human genomes sequenced and yet the vast majority of electronic health records have little if any genomic data. The causes for this deficiency have as much to do with physician education as technological limitations. I will discuss several recent projects show the way to scaleable incorporation of these data into the automated process of healthcare. These include the Undiagnosed Disease Network, multiple institution-specific oncogenomic applications, and the adoption of programmatic interfaces such as SMART/FHIR and their implementations in Sync4Science and commercial consumer platforms such as Apple’s iOS.
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