Table 1.
Nearest marker | Assay | Mean EC50 RIs, vol
%*
|
F ratio | P value† | % Vp | Location, map units‡ | |
---|---|---|---|---|---|---|---|
BO allele | N2 allele | ||||||
stP124 (IC) | Dispersal | 1.12 ± 0.12 | 0.69 ± 0.05 | 16.8 | 0.0001 | 22 | 0.4 |
stP6 (VR) | Dispersal | 0.58 ± 0.05 | 1.01 ± 0.07 | 23.2 | 0.000008 | 42 | 5.9 |
stP18 (VR) | Mating | 0.46 ± 0.02 | 0.66 ± 0.02 | 53.7 | 0.000000003 | 48 | 9.7 |
stP124 (IC) × stP98 (IIC) | Mating | NA | NA | 23.4 | 0.00003 | 11 | NA |
bP1 (VC) × stP129 (XC) | Mating | NA | NA | 32.9 | 0.000003 | 16 | NA |
Mean ± SEM of the EC50s for all strains with either the BO or the N2 allele at that marker.
Bonferroni-corrected significance thresholds are 0.05/11 = 0.0045 for single QTL and 0.05/55 = 0.0009 for interacting QTLs. Only single QTLs that are also significant at the 0.05 level by experiment-wise permutation are listed. The F ratios/P values for the interacting QTLs are for the interaction term of the regression equation.
Location of the peak likelihood ratio by interval mapping relative to the standard C. elegans genetic map.
NA, not available.