knitr::opts_chunk$set( collapse = TRUE, comment = "#>" ) s_bib_path <- "bibliography.bib" met <- rmdhelp::MendeleyExportToolR6$new() met$set_local_bib_file(ps_local_bib_file = s_bib_path)
library(qzwslrm)
The comparison between PBLUP and GBLUP evaluation is described in this document. In the paper r met$add("Legarra2018")
available at https://link.springer.com/article/10.1186/s12711-018-0426-6, this special comparison is explained on page 10.
The addition of marker data to a pedigree based evaluation which corresponds to moving from a PBLUP to a (SS)GBLUP evaluation can also be viewed as having more data. Thus a way to check the increase in accuracy caused by the addition of marker data in a genetic evaluation is to view the data with marker information as the "whole" dataset and the data without marker as the "partial" dataset.
Using subscript $G$ to refer to EBV based on data with marker information and $A$ to EBV based on data without markers, this yields
$$\rho_{A,G} = \frac{\left( \hat{\mathbf{u}}_A - \overline{\hat{\mathbf{u}}}_A \right)^T \left( \hat{\mathbf{u}}_G - \overline{\hat{\mathbf{u}}}_G\right)} {\sqrt{\left( \hat{\mathbf{u}}_A - \overline{\hat{\mathbf{u}}}_A \right)^T \left( \hat{\mathbf{u}}_A - \overline{\hat{\mathbf{u}}}_A\right) \left( \hat{\mathbf{u}}_G - \overline{\hat{\mathbf{u}}}_G \right)^T \left( \hat{\mathbf{u}}_G - \overline{\hat{\mathbf{u}}}_G\right)}}
= \frac{acc_A}{acc_G} $$
This assumes $Cov(\hat{\mathbf{u}}_G, \hat{\mathbf{u}}_A) = Var(\hat{\mathbf{u}}_A)$ which has formally been proven only for a single marker that was fitted as a correlated trait (r met$add("Legarra2015a")
). The procedure above uses the same phenotypes for evaluations with either $G$ or $A$. An alternative approach might be to compare the increase in accuracy from partial to whole in both in both approaches. In this case the following procedure is proposed
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