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. 2016 Jul 7;39(3):398–407. doi: 10.1590/1678-4685-GMB-2015-0232

Table 4. Genome-wide association of 13 tested traits under the normal condition (NC) and the PEG-induced, simulated drought-stress condition (SC) detected using general linear (GLM) and mixed linear (MLM) models. For trait abbreviations see Table 1.

Trait GLM MLM No. Sharec
No.siga Average -log(P) Range -log(P) Average R2 (%)b Range R2 (%) b No.siga Average -log(P) Range -log(P) Average R2 (%) b Range R2 (%)b
NC FRS 31 4.476 3.843-5.522 4.958 4.183-6.240 1 3.970 4.732 1
RD 9 4.055 3.884-4.334 4.367 4.160-4.702
RDW 1 4.314 4.891
RFW 28 4.555 3.873-6.217 5.087 4.243-7.128
RL 16 4.734 3.866-7.607 4.912 3.896-8.144
RT 12 4.635 3.858-5.551 4.674 3.866-6.016 1 3.980 4.805
SDW 5 4.703 3.855-6.332 4.983 3.983-6.860 1 4.040 4.803 1
SFW 7 4.564 3.878-6.596 4.883 4.074-7.277 2 4.122 4.109-4.136 4.932 4.912-4.951 2
SH 1 3.932 4.410
TDW 9 4.567 3.901-6.883 4.826 4.044-7.508 1 4.217 5.033 1
TFW 21 4.763 3.875-6.930 5.116 4.062-7.653 2 3.893 3.857-3.930 4.566 4.516-4.616 2
TNOR 11 4.701 3.873-5.462 4.728 3.780-5.896 1 3.945 4.760 1
SC DRS 1 4.238 7.197
FRS 1 4.242 4.588
RD 8 5.628 3.875-7.932 6.569 4.319-9.367 6 5.793 3.844-6.505 8.140 4.995-9.211 5
RDW 6 4.184 3.959-5.076 4.404 4.129-5.395
RT 1 3.967 4.460
SFW 1 3.991 4.339
TDW 8 4.561 4.006-5.631 4.898 4.238-6.162 2 4.087 3.992-4.183 4.857 4.725-4.989 2
TFW 6 4.447 3.868-5.290 4.792 4.112-5.796 3 4.678 4.089-4.973 5.637 4.813-6.049 3
TNOR 1 4.148 4.708
DI DRS 1 4.639 5.288 1 5.286 9.930 1
FRS 7 4.264 3.868-5.330 4.965 4.370-6.229
RD 3 4.432 4.432-4.432 5.154 5.154-5.154 3 4.225 4.225-4.225 5.133 5.133-5.133 3
RL 1 4.425 4.979 1 3.848 4.513 1
RT 3 4.323 3.872-4.906 5.228 4.415-6.447 1 4.401 5.838 1
SDW 5 4.850 4.421-5.085 5.625 5.064-5.907
TDW 2 4.274 4.059-4.490 4.902 4.604-5.199
TNOR 3 4.366 3.982-4.872 5.280 4.554-6.395 1 4.396 5.818 1
Total 208 28 25
a

Total number of significantly associated SNPs detected by GLM and MLM at the threshold of -log10 p = 3.839

b

R2 value showing the percentage of explained phenotypic variation

c

Number of significant SNPs detected by both models