FinnGen data
Questions related to retrieval and contents of FinnGen data.
Questions in this section
I think I found a mistake in the longitudinal data?
What are the field/column names in FinnGen?
What covariates are used in FinnGen's core GWAS analyses?
Does FinnGen have lab results available?
Does FinnGen have family and relatedness information available?
Where can I find a list of unrelated individuals in FinnGen?
When moving from BCOR to .txt files, what does the column called "correlation" mean?
What's the difference between phenotype_2.0 and phenotype_3.0?
Is there really no participant birth year data?
How do I calculate time between events?
Can I select only the columns needed for my analysis to import into RStudio?
How do I get patient IDs for analysis?
What is the difference between LD-clumping and the Saige conditional analysis?
Can I download all pairwise LD data across the genome at once?
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