|  |  | Genotyped | Ungenotyped |
---|
EBV | h2 | CONBLUP | NM | HAP2 | HAP4 | NM | HAP2 | HAP4 |
QTL | 0.03 | Â | 0.867 | 1.115 | 1.143 | 0.797 | 1.109 | 1.165 |
 | 0.10 |  | 0.772 | 0.899 | 0.955 | 0.809 | 0.889 | 0.953 |
 | 0.30 |  | 0.869 | 0.909 | 0.917 | 0.744 | 0.884 | 0.910 |
Polygenic | 0.03 | Â | 0.945 | 0.962 | 0.970 | 0.948 | 0.965 | 0.975 |
 | 0.10 |  | 0.950 | 0.973 | 0.985 | 0.951 | 0.973 | 0.985 |
 | 0.30 |  | 0.951 | 0.966 | 0.976 | 0.954 | 0.965 | 0.973 |
Total | 0.03 | 0.972 | 0.954 | 0.991 | 0.986 | 0.989 | 0.997 | 0.989 |
 | 0.10 | 0.987 | 0.981 | 0.975 | 0.974 | 1.022 | 1.014 | 1.011 |
 | 0.30 | 0.966 | 1.000 | 0.988 | 0.979 | 1.032 | 1.029 | 1.026 |
- Regression1 of true on estimated breeding values for QTL-EBV, polygenic EBV and total EBV for genotyped males and ungenotyped females for different values of heritability for marker-assisted BLUP with neighboring marker (NM), 2-marker haplotype (HAP2) and 4-marker haplotypes (HAP4) and conventional BLUP (CONBLUP) (sires and males in last generation are genotyped; distance between markers is 0.1 cM, the QTL explains 15% of the genetic variance, results are averages of 200 replicates)
- 1Standard errors were between 0.015 and 0.060 for QTL_EBV, between 0.004 and 0.015 for polygenic EBV and between 0.004 and 0.014 for total EBV; regressions where the variance of the predicted nhc was smaller than 0.0001 were omitted (denominator of regression coefficient)