Table 4.
Germplasm with desirable alleles for HSW identified by significant markers
| Trait | Marker | CChro | Highest positive a | Highest negative b | ||||
|---|---|---|---|---|---|---|---|---|
| Allele | Effect | Germplasm | Allele | Effect | Germplasm | |||
| HSW | Satt365 | 6 | 245:245 | 8.00 | As50 | 260:260 | 4.85 | As37 |
| HSW | Satt590 | 7 | 390:390 | 7.50 | As50 | 275:275 | 6.54 | As8 |
| HSW | Satt581 | 10 | 144:144 | 3.26 | As50 | 170:170 | 7.89 | As29–31 |
| HSW | Satt331 | 10 | 204:204 | 10.86 | As50 | 250:250 | 1.64 | As8 |
| HSW | Satt358 | 10 | 205:205 | 10.11 | As17 | 145:145 | 8.25 | As29–31 |
| HSW | Satt519 | 11 | 310:310 | 8.07 | As50 | 312:312 | 1.39 | As51 |
| HSW | Satt252 | 13 | 215:215 | 10.40 | As50 | 195:195 | 5.55 | As30–31 |
| HSW | Satt560 | 14 | 305:305 | 7.00 | As50 | 340:340 | 3.53 | Am48 |
| HSW | Satt186 | 17 | 197:197 | 4.67 | As50 | 255:255 | 6.99 | As30 |
| HSW | Satt372 | 17 | Nil | Nil | Nil | 300:300 | 12.17 | As29 |
| HSW | Satt564 | 18 | 220:220 | 11.60 | As28 | 130:130 | 4.02 | Af13–15 |
| HSW | Satt527 | 19 | 250:250 | 7.95 | A38 | 225:225 | 0.34 | Af40–42; As30,31,40 |
| HSW | Satt571 | 20 | 145:145 | 4.85 | As17,48 | 200:200 | 3.54 | Af42,52 |
a and b indicate alleles and their effect on each trait and germplasm with those alleles. Alleles with positive and negative effects increase and decrease phenotype, respectively