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Science Spotlight | August

Upsana Tayal MD |Sanjay Prasad MD FACS | Stuart Cook  PhD

08/09/2017

 

Identifying rare and common genetic variants contributing to systolic heart failure has been challenging given given its diverse and multiple etiologies. DCM, however although rarer,is a reasonably specific and well defined condition, leading to identification of many rare genetic variants.

Extracting Research-Quality Phenotypes from Electronic Health Records to Support Precision Medicine

Wei-Qi Wei MD PhD | Joshua Denny MD MS

08/13/2017

 

The convergence of two rapidly developing technologies - high-throughput genotyping and electronic health records (EHRs) - gives scientists an unprecedented opportunity to utilize routine healthcare data to accelerate genomic discovery.

 

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