Arnav Lal collects water at Playa Baquerizo on San Cristóbal Island as a sea lion watches.
(Image: Lisa Mattei)
Individual genes have the ability to influence more than one trait or characteristic. But this feature is often discovered through a type of analysis called pleiotropy, which requires merging a patient’s data from electronic health records at many different places—a challenge given privacy stipulations. A team at the Perelman School of Medicine created a new method that could make pleiotropy easier to perform and more widely used, called Sum-Share. The statistical model pulls summary-level information from many different sites to generate significant insights.
In a test of the method, published in Nature Communications, Sum-Share’s developers detected more than 1,700 DNA-level variations that could be associated with five different cardiovascular conditions. Using patient-specific information from just one site, which is the current norm, would have found just one variation.
This story is by Frank Otto. Read more at Penn Medicine News.
From Penn Medicine News
Arnav Lal collects water at Playa Baquerizo on San Cristóbal Island as a sea lion watches.
(Image: Lisa Mattei)
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Nhlanhla Mavuso of Fluid Silicon at work in the Moore Building.
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