Intersection of rare pathogenic variants from TCGA in the All of Us Research Program v6

Intersection of rare pathogenic variants from TCGA in the All of Us Research Program v6

Summary: Using rare cancer predisposition alleles derived from The Cancer Genome Atlas (TCGA) and high cancer prevalence (14% of participants) in All of Us (version 6), we assessed the impact of these rare alleles on cancer occurrence in six broad groups of genetic similarity provided by All of Us:...

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Bibliographic Details
Main Authors: Blaine A. Bates, Kylee E. Bates, Spencer A. Boris, Colin Wessman, David Stone, Justin Bryan, Mary F. Davis, Matthew H. Bailey
Format: Article
Language:English
Published: Elsevier 2025-04-01
Series:HGG Advances
Subjects:
MeSH
neoplasms
genetic predisposition to disease
diverse genetics
genotype-phenotype association
phenome-wide association study
Online Access:http://www.sciencedirect.com/science/article/pii/S2666247725000089
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http://www.sciencedirect.com/science/article/pii/S2666247725000089

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