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Expanded the interpretation and biases section. Removed most of the contrasts with twin studies and intelligence since these are unrelated to GCTA estimates and make this entry not self-contained. Tag: references removed |
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* LDAK:<ref>Speed et al 2016, [http://biorxiv.org/content/early/2017/01/15/074310 "Re-evaluation of SNP heritability in complex human traits"]</ref> loosens the GCTA assumption that all SNPs, regardless of genotyping quality or frequency, have same averaged expected effect, allowing for potentially finding much more SNP heritability
* GREML-IBD:<ref name="Evans2017B">Evans et al 2017, [http://www.biorxiv.org/content/early/2017/07/17/164848 "Narrow-sense heritability estimation of complex traits using identity-by-descent information."]</ref> GCTA for [[identity by descent]], attempting to estimate heritability based on shared genome segments in distant otherwise-unrelated relatives, in order to capture the effect of rarer variants which are not measured by SNP panels or otherwise imputed
== See also ==
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