Table 2.
QTL mapping results: ‘a’ is the additive genotypic value (half the difference between the two homozygotes), ‘d’ is the dominance genotypic value (deviation of the heterozygote from the midpoint of the two homozygotes), CI provides the genome coordinates of the confidence interval for the QTL
Chr |
Position (cM) |
Sex | LOD |
Corrected genome-wide probability |
5% chromosome-wise threshold |
5% genome-wise threshold |
a | d | R2 | CI (Mb) |
---|---|---|---|---|---|---|---|---|---|---|
10 | 23 | Both | 3.45 | 0.07 | 1.85 | 3.65 | 1.77 | 4.64 | 0.23 | 51.7–82.1 |
10 | 24 | Male | 4.43 | 0.0215 | 1.83 | 3.91 | 2.64 | 0.75 | 0.48 | 61.1–98.1 |
12 | 51.3 | Male | 4.09 | 0.0385 | 1.79 | 3.91 | −0.78 | 4.07 | 0.49 | 101.9–end |
Abbreviation: QTL, quantitative trait loci.