I haven’t read much at all about the Iterated Meiosis proposal but I’d be pretty concerned based on the current state of polygenic models that you end up selecting for a bunch of non-causal sites which were only selected as markers due to linkage disequlibrum (and iterated recombination makes the PRS a weaker and weaker predictor of the phenotype).
I haven’t read much at all about the Iterated Meiosis proposal but I’d be pretty concerned based on the current state of polygenic models that you end up selecting for a bunch of non-causal sites which were only selected as markers due to linkage disequlibrum (and iterated recombination makes the PRS a weaker and weaker predictor of the phenotype).