Data sharing begins and ends with the cancer patient. Through informed consent, the patient authorizes her data for use in research. In the center are the people using her data. This includes researchers and people working in funding agencies, institutions, and the technology fields. The gold ring shows ODS’ role, supporting programs, processes, and policy needs. The outer ring shows steps in data sharing, starting with identifying research needs and approaches, and applying for funding (shown in purple); followed by generating, collecting, and submitting data (in mauve); accessing, using, and retaining data (in teal); and ending in better treatments and therapies for cancer patients.
Find training resources, opportunities to collaborate, advice from NCI data science experts, and ways to network and engage with the cancer data science community on our NCI Cancer Data Science page!