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:...
Saved in:
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: | |
Online Access: | http://www.sciencedirect.com/science/article/pii/S2666247725000089 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
The interplay of sex and genotype in disease associations: a comprehensive network analysis in the UK Biobank
by: Vivek Sriram, et al.
Published: (2025-01-01) -
Clinical and genetic associations for night eating syndrome in a patient biobank
by: Hannah Wilcox, et al.
Published: (2024-12-01) -
How data science and AI-based technologies impact genomics
by: Jing Lin, et al.
Published: (2023-01-01) -
Do Major Pharmacovigilance Databases Support Evidence of Second Trimester NSAID and Third Trimester Paracetamol Fetotoxicity?
by: Katarina Dathe, et al.
Published: (2024-11-01) -
Genetics of Inflammatory Bowel Disease: Current Understanding and Future Directions
by: P. K. Chandra Sekar, et al.
Published: (2024-12-01)