15 Sep Discovery Radio Episode 113: Data Collection: The Roots of Research
Collection of reliable data is essential to research, whether building a database for studying a specific condition or in building a database for conducting research related to multiple diseases. Discover Data Collection: The Roots of Research…inside this edition of CTSI Discovery Radio!
Guest
Ashima Singh, PhD, MS
Assistant Professor, Research Scientist, Institute for Health & Equity
Principal Investigator, Sickle Cell Database Collection program, Medical College of Wisconsin
Karen Dotson
Program Director, All of Us Research Program, Clinical and Translational Science Institute, Medical College of Wisconsin

Jenna Koney
Program Operations Manager, All of Us Research Program, Clinical and Translational Science Institute, Medical College of Wisconsin
More Information
- Sickle Cell Disease (NIH)
https://www.nhlbi.nih.gov/health/sickle-cell-disease - Sickle Cell Data Collection Program (CDC)
https://www.cdc.gov/ncbddd/hemoglobinopathies/scdc.html - The Bloodline – SCDC Quarterly Newsletter (CDC)
https://www.cdc.gov/ncbddd/hemoglobinopathies/scdc-newsletter.html - Sickle Cell Data Collection Program Summit (CDC)
https://www.cdc.gov/ncbddd/sicklecell/scdc-summit.html - All of Us Research Program – National (NIH)
https://www.joinallofus.org - All of Us Research Program – Milwaukee (MCW)
https://mcw.joinallofus.org/en - All of Us Research Program – Wisconsin
https://www.joinallofus.org/wisconsin - All of Us Research Hub (NIH)
https://www.researchallofus.org