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This is it: The Last Chance for EHR Stimulus Funds! Webinar
2014-07-31    
10:00 am - 11:00 am
Contact: Robert Moberg ChiroTouch 9265 Sky Park Court Suite 200 San Diego, CA 92123 Phone: 619-528-0040 ChiroTouch to Host This is it: The Last Chance [...]
RCM Best Practices
2014-07-31    
2:00 pm - 3:00 pm
In today’s cost-conscious healthcare environment every dollar counts. Yet, inefficient billing processes are costing practices up to 15% of their revenue annually. The areas of [...]
Aprima 2014 User Conference and VAR Summit
2014-08-08    
12:00 am
Aprima 2014 User Conference and VAR Summit Vendor Registration Thank you for your interest in participating in the Aprima 2014 User Conference and VAR Summit. Please [...]
Innovations for Healthcare IT
2014-08-10    
All Day
At Innovations for Healthcare IT, you'll discover new techniques and methods to maximize the use of your Siemens systems and help you excel in today's [...]
Consumerization of Healthcare
2014-08-13    
1:00 pm - 1:30 pm
Join Our Complimentary Express Webinar for an overview of “The Consumerization of Healthcare” on Wednesday, August 13th at 1:00 pm ET. Consumerism in the healthcare [...]
How to use HIPAA tracking software to survive an audit
2014-08-20    
2:00 pm - 3:30 pm
Wednesday, August 20th from 2:00 – 3:30 EST You have done a great job with Meaningful Use but will you pass a HIPAA audit?  Bob Grant, HIPAA auditor and expert will show you how to achieve total compliance and [...]
How Healthy Is Your Practice?
2014-08-27    
2:00 pm - 3:00 pm
According to recent statistics from MGMA, the typical physician practice leaves up to 30% of their potential revenue on the table every year. This money [...]
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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.

source