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pancancer_pleiotropy

This README file accompanies the following 17 files that contain GWAS summary statistics for 17 cancers based on a meta-analysis of the UK Biobank and GERA cohorts.

A description of how these summary statistics were generated and applied to investigate heritability and pan-cancer pleiotropy can be found here:

Rashkin et al., Pan-Cancer Study Detects Novel Genetic Risk Variants and Shared Genetic Basis in Two Large Cohorts, bioRxiv 2019

Files are stored with Git Large File Storage (Git-LFS).

Columns for each of the files listed above are as follows:

Column Name Description
CHR chromosome
BP basepair position in hg19/build 37
uniqID variant name
A1 effect allele
A2 other allele
N number of studies (N=1 for variants in UKB or GERA only)
P p-value (fixed effects meta-analysis)
P_random p-value (random effects meta-analysis)
OR odds ratio (fixed effects)
OR_random odds ratio (random effects)
Q p-value for Cochran’s Q heterogeneity test
I I^2 heterogeneity index (0-100)
ID variant name (rsID)
totN sample size

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Pan cancer summary statistics from meta analyses of UK Biobank and Kaiser GERA cohorts.

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