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Transforming Medicine: Evidence-Driven mHealth
2015-09-30 - 2015-10-02    
8:00 am - 5:00 pm
September 30-October 2, 2015Digital Medicine 2015 Save the Date (PDF, 1.23 MB) Download the Scripps CME app to your smart phone and/or tablet for the conference [...]
Health 2.0 9th Annual Fall Conference
2015-10-04 - 2015-10-07    
All Day
October 4th - 7th, 2015 Join us for our 9th Annual Fall Conference, October 4-7th. Set over 3 1/2 days, the 9th Annual Fall Conference will [...]
2nd International Conference on Health Informatics and Technology
2015-10-05    
All Day
OMICS Group is one of leading scientific event organizer, conducting more than 100 Scientific Conferences around the world. It has about 30,000 editorial board members, [...]
MGMA 2015 Annual Conference
2015-10-11 - 2015-10-14    
All Day
In the business of care delivery®, you have to be ready for everything. As a valued member of your organization, you’re the person that others [...]
5th International Conference on Wireless Mobile Communication and Healthcare
2015-10-14 - 2015-10-16    
All Day
5th International Conference on Wireless Mobile Communication and Healthcare - "Transforming healthcare through innovations in mobile and wireless technologies" The fifth edition of MobiHealth proposes [...]
International Health and Wealth Conference
2015-10-15 - 2015-10-17    
All Day
The International Health and Wealth Conference (IHW) is one of the world's foremost events connecting Health and Wealth: the industries of healthcare, wellness, tourism, real [...]
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MGMA 2015 Annual Conference
11 Oct 15
Nashville
Events on 2015-10-15
research papers

Researchers repurpose genetic data, EMR to perform large-scale PheWAS study

genetic data

Vanderbilt University Medical Center researchers and co-authors from four other U.S. institutions from the Electronic Medical Records and Genomics (eMERGE) Network are repurposing genetic data and electronic medical records to perform the first large-scale phenome-wide association study (PheWAS), released today in Nature Biotechnology.

Traditional genetic studies start with one phenotype and look at one or many genotypes, PheWAS does the inverse by looking at many diseases for one genetic variant or genotype.

“This study broadly shows that we can take decades of off-the-shelf electronic medical record data, link them to DNA, and quickly validate known associations across hundreds of previous studies,” said lead author Josh Denny, M.D., M.S., Vanderbilt Associate Professor of Biomedical Informatics and Medicine. “And, at the same time, we can discover many new associations.

“A third important finding is that our method does not select any particular disease – it is searches simultaneously for more than a thousand diseases that bring one to the doctor. By doing this, we were able to show some genes that are associated several diseases or traits, while others are not,” he added.

Researchers used genotype data from 13,835 individuals of European descent, exhibiting 1,358 diseases collectively. The team then ran PheWAS on 3,144 single-nucleotide polymorphisms (SNP’s), checking each SNP’s association with each of the 1,358 disease phenotypes.

As a result, study authors reported 63 previously unknown SNP-disease associations, the strongest of which related to skin diseases.

“The key result is that the method works,” Denny said. “This is a robust test of PheWAS across all domains of disease, showing that you can see all types of phenotypes in the electronic medical record – cancers, diabetes, heart diseases, brain diseases, etc. – and replicate what’s known about their associations with various SNPs.”

An online PheWAS catalog spawned by the study may help investigators understand the influence of many common genetic variants on human conditions.

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