Content-Length: 47256 | pFad | http://registry.opendata.aws/kids-first
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cancer genetic genomic Homo sapiens life sciences pediatric STRIDES structural birth defect whole genome sequencing
The NIH Common Fund's Gabriella Miller Kids First Pediatric Research Program’s (“Kids First”) vision is to “alleviate suffering from childhood cancer and structural birth defects by fostering collaborative research to uncover the etiology of these diseases and by supporting data sharing within the pediatric research community.” The program continues to generate and share whole genome sequence data from thousands of children affected by these conditions, ranging from rare pediatric cancers, such as osteosarcoma, to more prevalent diagnoses, such as congenital heart defects. In 2018, Kids First launched the Gabriella Miller Kids First Data Resource Center, charged with building a large-scale data platform supporting clinical and genetic data from these patients and their families in order to accelerate discovery and ultimately clinical impact. Researchers can search, access, aggregate, and analyze these data through the Kids First Data Resource Portal. Additionally, by using cloud-based individual workspaces in CAVATICA, a data analysis and sharing computation platform, researchers can cross-analyze Kids First data with data from other efforts, such as NCI’s TARGET program and consortia-based datasets like the Children’s Brain Tumor Tissue Consortium (CBTTC). Kids First is made available on AWS via the NIH STRIDES Initiative.
Data is updated on a rolling basis by the KFDRC to make data available as rapidly as possible under the NIH Genomic Data Sharing Policy.
NIH Genomic Data Sharing Policy: https://gdc.cancer.gov/access-data/data-access-policies
See all datasets managed by The Gabriella Miller Kids First Data Resource Center at the Children's Hospital of Philadelphia.
Gabriella Miller Kids First Pediatric Research Program (Kids First) was accessed on DATE from https://registry.opendata.aws/kids-first.
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