Trick is to rely on cheaper to measure, but genetically informative phenotypes with tons of variables that allow for effective use of machine learning methods. A kind of middle way. Presumably works well because fewer variables than full marker set of genotypes.
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And that the useful predictors are less rare among the chemical or spectrometer variables than among the genotypes, for which only like 1 in 100k is relevant or something which requires a lot of penalization to avoid overfitting.
End of conversation
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Comparison of Genotypic and Phenotypic Correlations: Cheverud’s Conjecture in Humanshttps://www.biorxiv.org/content/early/2018/03/30/291062 …
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