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7th World Congress on Public Health, Nutrition & Epidemiology
2019-05-15 - 2019-05-16    
All Day
May 15-16, 2019 Singapore Theme: Empowering Public Health and Advancing Health Equity About Conference The 7th World Congress on Public Health, Epidemiology & Nutrition will [...]
3rd International Genetics and Molecular Biology Conference
2019-05-17 - 2019-05-18    
All Day
Building on the strong connection and networking at our previous meetings, we are pleased to announce that the 3rd International Genetics and Molecular Biology Conference is scheduled [...]
7th International Conference on Food Chemistry and Technology
2019-05-20 - 2019-05-21    
All Day
Be a part of7th International Conference on Food Chemistry and Technology THEME:OPTIMIZING THE TRENDS AND TECHNIQUES IN FOOD CHEMISTRY AND TECHNOLOGY 7th International Conference on Food Chemistry and Technology has been [...]
Events on 2019-05-15
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.

source