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Surveillance Epidemiology and End Results (RRID:SCR_006902)
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Resource Information

URL: http://seer.cancer.gov/

Proper Citation: Surveillance Epidemiology and End Results (RRID:SCR_006902)

Description: SEER collects cancer incidence data from population-based cancer registries covering approximately 47.9 percent of the U.S. population. The SEER registries collect data on patient demographics, primary tumor site, tumor morphology, stage at diagnosis, and first course of treatment, and they follow up with patients for vital status.There are two data products available: SEER Research and SEER Research Plus. This was motivated because of concerns about the increasing risk of re-identifiability of individuals. The Research Plus databases require more rigorous process for access that includes user authentication through Institutional Account or multiple-step request process for Non-Institutional users.

Abbreviations: SEER

Synonyms: Surveillance Epidemiology and End Results (SEER) Program, Surveillance Epidemiology End Results, Surveillance Epidemiology End Results (SEER) Program

Resource Type: data set, data or information resource, report, narrative resource, database

Keywords: cancer, statistics, epidemiology, registry, mortality, cancer mortality, african-american, hispanic, american-indian, alaska native, asian, hawaiian, pacific islander, demographic, tumor site, tumor morphology, stage, treatment, follow-up, vital status, FASEB list

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This resource

is listed by

re3data.org

has parent organization

National Cancer Institute

is parent organization of

SEER Datasets and Software

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