CR3 News Magazine 2022 VOL 3: MAY -- MEDICAL | Page 68

in the field. It’s also designed with team science in mind, allowing researchers to explore topics in an open and collaborative way,” said Gail Jarvik, M.D., Ph.D., head of the Division of Medical Genetics at the University of Washington School of Medicine, Seattle. “As the Researcher Workbench matures, it will create nearly endless possibilities for discovery to understand the role of genes and variants, as well as many other factors that combine to affect health and disease.”

The Researcher Workbench is made possible through the generous contributions of  All of Us  participants. Beyond making genomic data available for research, All of Us participants have the opportunity to receive personal DNA results at no cost to them. So far, the program has offered genetic ancestry and trait results to more than 100,000 participants. Plans are under- way to begin to share health-related DNA results on hereditary disease risk and medication-gene interactions later this year.

With this release of genomic data,  All of Us  now ranks among other large genomic research efforts worldwide, including the UK Biobank, the Million Veteran Program and the NIH’s Trans-Omics for Precision Medicine (TOPMed) program.

All of Us  works with a  consortium of partners  across the U.S. to help reach participants and collect data and samples, including community organizations, medical centers and others. The Researcher Workbench is managed by Vanderbilt University Medical Center in collaboration with the Broad Institute of MIT and Harvard and Verily. The program’s genome centers generate the genomic data and process about 5,000 participant samples each week. These centers include Baylor College of Medicine, Johns Hopkins University, the Broad Institute, the Northwest Genomics Center at the University of Washington and partners. Color, a health technology company, works with the program to return personalized results to participants on genetic ancestry and traits, and the forthcoming health-related genetic results.

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To learn more about  All of Us  data and resources for researchers, or to register for access, go to  ResearchAllofUs.org. To learn more about getting involved as a research participant, visit JoinAllofUs.org.

All of Us  is a registered service mark of the U.S. Department of Health & Human Services (HHS).

About the  All of Us  Research Program: 

The mission of the All of Us  Research Program is to accelerate health research and medical breakthroughs, enabling individualized prevention, treatment, and care for all of us. The program will partner with one million or more people across the United States to build the most diverse biomedical data resource of its kind, to help researchers gain better insights into the biological, environmental, and behavioral factors that influence health. For more information, visit

 www.ResearchAllofUs.orgwww.JoinAllofUs.org, and 

https://www.AllofUs.nih.gov.

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