Using existing pediatric cancer data from the Gabriella Miller Kids First Data Resource Program

Author:

Hudson Alexandra1,Fournier Marcia2,Coulombe James2,Daee Danielle3ORCID

Affiliation:

1. Center for Research Strategy, National Cancer Institute , Bethesda, MD, USA

2. Developmental Biology and Congenital Anomalies Branch, Eunice Kennedy Shriver National Institute of Child Health and Human Development , Bethesda, MD, USA

3. Genomic Epidemiology Branch, Division of Cancer Control and Population Sciences, National Cancer Institute, Bethesda, MD, USA

Abstract

Abstract Childhood cancer and birth defects are leading causes of childhood mortality, and studies suggest that birth defects increase pediatric cancer risk. The Gabriella Miller Kids First Pediatric Research Program (Kids First) seeks to alleviate these conditions by building an expansive resource of genetic and clinical data from patients with pediatric cancer and birth defects and their families. This article describes the data and support provided by the Kids First Data Resource Center and the Kids First Data Resource Center Data Resource Portal, which enables the public to review Kids First studies and request access to individual data. The Kids First Portal contains data from more than 34 000 participants and connects with CAVATICA (Seven Bridges Genomics, Inc, now part of Velsera), a cloud-based analysis and sharing platform. Researchers have used Kids First data to investigate a variety of cancers and further funding opportunities are available. The Kids First Portal is a unique resource that unites pediatric cancer and birth defects to uncover their genetic etiology and improve patients’ lives.

Funder

NIH

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

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