Abstract
The multimodal data assembled through All of Us Research Program with enriched recruitment of populations underrepresented in biomedical research have provided a rich resource for equitable health research. The complexity of the All of Us research platform, however, is a common hurdle at the initiation of studies. This tutorial aims to demonstrate to researchers a practical, transparent and reproducible workflow for streamlining data curation and analysis. This tutorial covers modules: (1) design of All of Us studies; (2) selecting study cohort; (3) curating multimodal data (electronic health records, surveys, genomics, and wearable devices); (4) harmonizing disease onset outcomes in risk models. We showcased the proposed workflow using a case study for genetic risk prediction of rheumatoid arthritis for minority race/ethnicity groups. Step-by-step guides are provided in the supplementary materials and the online repository with links to SQL/R/Python example code and All of Us user interface operations.
| Original language | English (US) |
|---|---|
| Journal | Statistics in Biosciences |
| DOIs | |
| State | Accepted/In press - 2026 |
Bibliographical note
Publisher Copyright:© The Author(s) 2026.
Keywords
- Electronic health records
- Genetic risks
- Phenotyping
- Rheumatoid arthritis
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