Cross disease variant lookup in CBTN

Ongoing
Data
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CBTN Data Used

About this

Project

This project aims at identifying variants in the CBTN germline DNA whole genome sequencing data that are reported and/or found in other diseases, esp. birth defects and rare Mendelian disorders, hoping to explain/reveal shared genetics between pediatric cancer and rare diseases.

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Scientists

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Specimen Data

The Children's Brain Tumor Network contributed to this project by providing access to the Pediatric Brain Tumor Atlas.

Explore the data in these informatics portals

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