Opportunities to Advance Research for Children, Adolescents, and Young Adults with Cancer through Secondary Data Sharing in the New National Childhood Cancer Registry Data Platform

Are you interested in working with the latest data from childhood cancer research? Don’t miss this opportunity to learn about the Childhood Cancer Data Initiative’s National Childhood Cancer Registry (NCCR) and its new data platform in an upcoming NIH Data Sharing and Reuse Seminar! Johanna Goderre, technical lead for NCCR, will discuss:

• how the NCCR collaborates with children's hospitals, cancer centers, and oncology providers.
• the importance of incorporating diverse data sources, including genomic information and social determinants of health.
• how researchers, including students, can access this valuable data for secondary analysis.

The NCCR aims to revolutionize the way we collect and share childhood cancer data by connecting central cancer registries, healthcare providers, and researchers. This innovative data platform integrates population-based cancer registry data with real-world insights, enhancing our understanding of cancer in children, adolescents, and young adults.

This webinar is part of the NIH Data Sharing and Reuse Seminar Series, which is hosted by the NIH Office of Data Science and Strategy. The monthly series highlights researchers who have taken existing data and found clever ways to reuse the data or generate new findings.