| 000 | 03391nab|a22003857a|4500 | ||
|---|---|---|---|
| 001 | 68663 | ||
| 003 | MX-TxCIM | ||
| 005 | 20251223150141.0 | ||
| 008 | 25022822025||||-us||p|op||||00||0|eengdd | ||
| 022 | _a2160-1836 | ||
| 024 | 8 | _ahttps://doi.org/10.1093/g3journal/jkaf031 | |
| 040 | _aMX-TxCIM | ||
| 041 | _aeng | ||
| 100 | 1 |
_aTessele, A. _938420 |
|
| 245 | 1 | 0 | _aImproving genomic selection in hexaploid wheat with sub-genome additive and epistatic models |
| 260 |
_aBethesda, MD (United States of America) : _bOxford University Press, _c2025. |
||
| 500 | _aPeer review | ||
| 500 | _aOpen Access | ||
| 520 | _aThe goal of wheat breeding is the development of superior cultivars tailored to specific environments, and the identification of promising crosses is crucial for the success of breeding programs. Although genomic estimated breeding values were developed to estimate additive effects of genotypes before testing as parents, application has focused on predicting performance of candidate lines, ignoring non-additive genetic effects. However, non-additive genetic effects are hypothesized to be especially important in allopolyploid species due to the interaction between homeologous genes. The objectives of this study were to model additive and additive-by-additive epistatic effects to better delineate the genetic architecture of grain yield in wheat and to improve the accuracy of genomewide predictions. The dataset utilized consisted of 3740 F5:6 experimental lines tested in the K-State wheat breeding program across the years 2016 and 2018. Covariance matrices were calculated based on whole and sub-genome marker data and the natural and orthogonal interaction approach (NOIA) was used to estimate variance components for additive and additive-by-additive epistatic effects. Incorporating epistatic effects in additive models resulted in non-orthogonal partitioning of genetic effects but increased total genetic variance and reduced deviance information criteria. Estimation of sub-genome effects indicated that genotypes with the greatest whole genome effects often combine sub-genomes with intermediate to high effects, suggesting potential for crossing parental lines which have complementary sub-genome effects. Modeling epistasis in either whole-genome or sub-genome models led to a marginal (3%) improvement in genomic prediction accuracy, which could result in significant genetic gains across multiple cycles of breeding. | ||
| 546 | _aText in English | ||
| 597 |
_fBreeding for Tomorrow _dKansas Wheat Commission _dKansas Wheat Alliance, Inc. _uhttps://hdl.handle.net/10568/179269 |
||
| 650 | 7 |
_aAdditives _2AGROVOC _914443 |
|
| 650 | 7 |
_aGenomes _2AGROVOC _91131 |
|
| 650 | 7 |
_aHexaploidy _2AGROVOC _92020 |
|
| 650 | 7 |
_aWheat _2AGROVOC _91310 |
|
| 650 | 7 |
_aBreeding _2AGROVOC _91029 |
|
| 700 | 1 |
_aGonzález-Diéguez, D.O. _8I1707522 _gGlobal Wheat Program _gBreeding Modernization and Innovation Platform _926628 |
|
| 700 | 1 |
_aCrossa, J. _gGenetic Resources Program _8CCJL01 _959 |
|
| 700 | 1 |
_aJohnson, B.E. _938421 |
|
| 700 | 1 |
_aMorris, G.P. _94848 |
|
| 700 | 1 |
_aFritz, A.K. _93758 |
|
| 773 | 0 |
_tG3: Genes, Genomes, Genetics _gv. 15, no. 4, art. jkaf031 _dBethesda, MD (United States of America) : Oxford University Press, 2025. _x2160-1836 _w56922 |
|
| 856 | 4 |
_yOpen Access through DSpace _uhttps://hdl.handle.net/10883/35532 |
|
| 942 |
_cJA _n0 _2ddc |
||
| 999 |
_c68663 _d68655 |
||