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@dromar.eth
The multiple testing problem in GWAS perfectly illustrates why signal-to-noise is so challenging in personalized medicine: we're searching for maybe a few dozen causal genetic variants while running millions of statistical tests, each with a 5% false positive rate. With 1M variants, that's 50,000 "significant" results by chance alone - not even counting true biological effects.
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@dromar.eth
In statistics this is also called the false discovery rate or FDR
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