Skip to main content
. 2019 Dec 9;20:956. doi: 10.1186/s12864-019-6323-8

Table 2.

Mean (SD) of the “true” variance components and heritability in the base (founder) population (P-base) and the base population for the genomic phasea and estimates of variance components and heritabilities from P-AM, ssGBLUP, and ssBR based on three scenarios of phenotypingb

Method Scenariob σg2(σε2) σe2 σα2j=1m2pj1pj h2c
True VCs in P-base 3.59 (0.03) 5.05 (0.09) 0.42 (0.004)
True VCs in G-base 2.82 (0.09) 5.10 (0.07) 0.36 (0.009)
P-AM Pheno1 3.62 (0.12) 5.02 (0.02) 0.42 (0.009)
Pheno1 + 2 3.52 (0.06) 5.07 (0.03) 0.41 (0.004)
Pheno2 3.19 (0.20)* 5.21 (0.10) 0.38 (0.018)*
ssGBLUP Pheno1 2.99 (0.12)*** 5.54 (0.01)*** 0.35 (0.009)***
Pheno1 + 2 3.39 (0.06)*** 5.17 (0.03) 0.40 (0.009)***
Pheno2 3.36 (0.15)*** 5.19 (0.05) 0.39 (0.013)*
ssBR Pheno1 3.44 (0.15) 5.10 (0.04) 4.20 (0.10)*** 0.40 (0.012)
Pheno1 + 2 3.14 (0.10)*** 5.24 (0.02)* 3.71 (0.11) 0.37 (0.008)***
Pheno2 2.99 (0.20) 5.27 (0.06)** 2.97 (0.09) 0.36 (0.017)

aP-AM: traditional pedigree-based animal model; ssGBLUP: single-step genomic BLUP; ssBR: single-step Bayesian regression. σg2 is the genetic variance used in P-AM, σε2 is the total genetic variance used in ssBR; σe2 is the residual variance; σα2 is the marker variance; σα2j=1m2pj1pj is used to calculate genetic variance via the estimated marker variance in ssBR, where pj is the observed allele frequency at locus j, and m is the total number of markers

bPheno1: phenotypes from only the conventional phase (1–20 years) were used; Pheno1 + 2: phenotypes from both the conventional phase and genomic selection phase (1–35 years) were used; Pheno2: phenotypes from only the genomic selection phase were used (21–35 years)

cHeritabilities (h2) from P-AM, ssGBLUP, and ssBR calculated as σgε2σgε2+σe2

The significance test was performed to determine whether the estimated parameter differs from the simulated parameter. * significant at P < 0.01; ** significant at P < 0.005; *** significant at P < 0.001