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Updated: Jul 15, 2025

Detection and Monitoring of Tumor Associated Circulating DNA in Patient Biofluids
Published on: June 8, 2019
Using existing pediatric cancer data from the Gabriella Miller Kids First Data Resource Program
Alexandra Hudson1, Marcia Fournier2, James Coulombe2
1Center for Research Strategy, National Cancer Institute, Bethesda, MD, USA.
Insights
The Kids First program offers a valuable data resource for childhood cancer and birth defect research. This initiative aims to uncover genetic causes and improve outcomes for affected children.
Area of Science:
- Genomics
- Pediatric Research
- Bioinformatics
Background:
- Childhood cancer and birth defects are significant causes of mortality in children.
- Existing research suggests a link between birth defects and an increased risk of pediatric cancer.
- The Gabriella Miller Kids First Pediatric Research Program (Kids First) was established to address these critical health issues.
Purpose of the Study:
- To describe the data and support services offered by the Kids First Data Resource Center.
- To introduce the Kids First Data Resource Portal as a public platform for accessing research studies.
- To facilitate the investigation of the genetic etiology of pediatric cancer and birth defects.
Main Methods:
- The Kids First Data Resource Center compiles genetic and clinical data from pediatric cancer and birth defect patients and their families.
- The Kids First Data Resource Portal provides public access to review studies and request data.
- Data integration with CAVATICA, a cloud-based analysis and sharing platform, enhances data accessibility and research capabilities.
Main Results:
- The Kids First Portal hosts data from over 34,000 participants.
- The portal connects researchers with a comprehensive dataset for investigating pediatric diseases.
- The integrated platform supports diverse research inquiries into pediatric cancers and birth defects.
Conclusions:
- The Kids First Portal is a unique, centralized resource for pediatric cancer and birth defect research.
- Uniting genetic and clinical data aids in understanding the underlying causes of these conditions.
- This resource has the potential to significantly improve the lives of children affected by cancer and birth defects.
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.
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