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272 results for “childhood cancer”
French National Registry of Childhood Cancers
The registry includes all children newly diagnosed with cancer, younger than 18 years (since 2011), and whose usual residence is in mainland France or overseas departments at the time of diagnosis. RNCE made up of: The French National Registry of Childhood Haematological Malignancies, which records all diagnoses of haematological malignancies since 1990 and The French National Registry of Childhood Solid Tumours, which records all solid tumours cases since 2000. Until 2011, RNCE covered mainland France's under 15 population. Since 2011, it expanded to the overseas territories and teenagers under 18 years old.
Childhood and Adolescent Cancer, Texas 2014-2023
Cancer counts diagnosed among those age 0-19 years
Automated Childhood Cancer Information System
The Automated Childhood Cancer Information System (ACCIS) is an authoritative source of data on cancer incidence and survival of children and adolescents in Europe. The primary aim of the ACCIS project is to widely disseminate comprehensive information about the occurrence and outcome of various cancers in the young European population. The ACCIS results stimulate research and inform public health policies.
Childhood Cancer and Leukemia International Consortium
In 2007, the Childhood Leukemia International Consortium (CLIC) was founded to overcome the limitations of individual case-control studies of pediatric leukemias; and in 2019, CLIC began to accept studies of childhood solid tumors and changed its name to the Childhood Cancer and Leukemia International Consortium while retaining its original acronym. CLIC's mission is to develop and support collaborations among epidemiologists, clinicians, tumor biologists, geneticists, immunologists, toxicologists, and/or statisticians. Together, these scientists evaluate factors that influence the risk of childhood cancer through epidemiologic studies, genomic studies, and related research. CLIC currently focuses on studying childhood leukemias, brain tumors, and embryonal tumors. Most of these studies have detailed epidemiologic data, and about half have biospecimens or existing genomic data. The immense wealth of available data provides CLIC the unique opportunity to assess the individual and interactive effects of genetic and environmental risk factors on childhood cancers. This dataset contains case-control studies of childhood cancers with epidemiological data from CLIC's Data Coordinating Center at the International Agency for Research on Cancer (IARC). Together with data from other collaborating institutions, CLIC has the world's largest data repository addressing causes of childhood cancer, which allows to study etiology with great precision.
International Incidence of Childhood Cancer
International Incidence of Childhood Cancer (IICC) is a collaborative project of the International Agency for Research on Cancer (IARC) and the International Association of Cancer Registries (IACR). This project was co-sponsored by the Union for International Cancer Control (UICC). The objective is to disseminate the available data on the incidence of cancer in children around the world. This will be achieved through the publication of a monograph, the third volume in the IICC series (IICC-3). Both print and electronic versions are envisaged, with the first results to appear in 2017. Data from 440 registries in five continents have been collected, validated, analysed, and evaluated. More than 300 registries met the inclusion criteria and provided high-quality comparable datasets and they were selected for publication in IICC-3 after rigorous peer review by the IICC-3 Editors.
Childhood Cancer Survivor Study (CCSS)
Analysis of subsequent neoplasm genomes from childhood cancer survivors
Childhood Cancer Survivor Study (CCSS)
Open the record for dataset details and reuse information.
Childhood Cancer Survivor Study (CCSS)
Open the record for dataset details and reuse information.
Gabriella Miller Kids First Pediatric Research Program in Genetics at the Intersection of Childhood Cancer and Birth Defects
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Australian Childhood Cancer Registry
Consistent information is collected about staging and other prognostic indicators allowing us to benchmark and make international comparisons. The registry also collects information about treatment, relapses and second cancers making it one of the most comprehensive registries in the world. Data collection and analyses will continue with the goal of increasing the understanding of how cancer impacts Australian children. The Australian Childhood Cancer Statistics Online provides recent incidence, survival and mortality data by sex and age group for the most common cancers among children in Australia.
Childhood Cancer Survivor Study
The Childhood Cancer Survivor Study (CCSS) was established in the early 1990s as a cohort of more than 14,000 childhood cancer survivors from 26 centers in North America who were originally diagnosed between 1970 and 1986.
Kids First: Genetics at the Intersection of Childhood Cancer and Birth Defects
Namespace hosted on the Kids First DRC FHIR services at fhir.kidsfirstdrc.org
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.