Workshop: Making All of Us for all of us: Exploring how the All of Us genomic dataset has grown

The NIH’s All of Us Research Program is committed to collecting multiple types of health data from a million or more participants to create a diverse research resource that accelerates precision medicine. The All of Us Researcher Workbench is the free-to-access secure, cloud-based platform where registered researchers from both US-based and international intuitions access and analyze data using Python, R, or SAS coding languages. Currently the program has over 413,000 program participants with >245,000 whole genome sequence (WGS) samples and >314,000 genotyping arrays. Looking forward, we anticipate counts for both WGS and arrays to surpass 400,000 soon. The genomic data is combined with many types of phenotypic and auxiliary data types including electronic health records (EHR), survey data, physical measurements, and mobile health data (Fitbit). This session will 1) provide an interactive, guided demonstration of the public facing genomic tools, including the new PheWAS x GWAS data browser 2) provide an interactive, guided demonstration of our cloud computing platform, the Researcher Workbench 3) provide participants a hands-on opportunity to replicate a research study with new genomic data types including structural variant and long reads data and 4) conduct an interactive Q&A session to engage attendees about the All of Us Researcher Workbench and the novel technology implemented to conduct genomic analyses.

Please note, to participate in the interactive activities included in this workshop, please register for the platform. This process may take a few hours; registrants are strongly encouraged to complete this by November 15. Platform registration is optional but highly recommended.