000 | 03783nab|a22004577a|4500 | ||
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001 | 62827 | ||
003 | MX-TxCIM | ||
005 | 20240919021229.0 | ||
008 | 201030s2021||||gw |||p|op||||00||0|eng|d | ||
022 | _a0040-5752 | ||
022 | _a1432-2242 (Online) | ||
024 | 8 | _ahttps://doi.org/10.1007/s00122-020-03696-9 | |
040 | _aMX-TxCIM | ||
041 | _aeng | ||
100 | 1 |
_aAtanda, A.S. _8001711295 _8001712571 _gGlobal Maize Program _gFormerly Global Wheat Program _98531 |
|
245 | 1 | 0 | _aMaximizing efficiency of genomic selection in CIMMYT's tropical maize breeding program |
260 |
_aBerlin (Germany) : _bSpringer, _c2021. |
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500 | _aPeer review | ||
500 | _aOpen Access | ||
520 | _aKey message Historical data from breeding programs can be efficiently used to improve genomic selection accuracy, especially when the training set is optimized to subset individuals most informative of the target testing set. The current strategy for large-scale implementation of genomic selection (GS) at the International Maize and Wheat Improvement Center (CIMMYT) global maize breeding program has been to train models using information from full-sibs in a "test-half-predict-half approach." Although effective, this approach has limitations, as it requires large full-sib populations and limits the ability to shorten variety testing and breeding cycle times. The primary objective of this study was to identify optimal experimental and training set designs to maximize prediction accuracy of GS in CIMMYT's maize breeding programs. Training set (TS) design strategies were evaluated to determine the most efficient use of phenotypic data collected on relatives for genomic prediction (GP) using datasets containing 849 (DS1) and 1389 (DS2) DH-lines evaluated as testcrosses in 2017 and 2018, respectively. Our results show there is merit in the use of multiple bi-parental populations as TS when selected using algorithms to maximize relatedness between the training and prediction sets. In a breeding program where relevant past breeding information is not readily available, the phenotyping expenditure can be spread across connected bi-parental populations by phenotyping only a small number of lines from each population. This significantly improves prediction accuracy compared to within-population prediction, especially when the TS for within full-sib prediction is small. Finally, we demonstrate that prediction accuracy in either sparse testing or "test-half-predict-half" can further be improved by optimizing which lines are planted for phenotyping and which lines are to be only genotyped for advancement based on GP. | ||
546 | _aText in English | ||
650 | 7 |
_aMarker-assisted selection _2AGROVOC _910737 |
|
650 | 7 |
_aPlant breeding _gAGROVOC _2 _91203 |
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650 | 7 |
_aMaize _2AGROVOC _91173 |
|
700 | 1 |
_aOlsen, M. _8INT3333 _9923 _gGlobal Maize Program |
|
700 | 1 |
_aBurgueƱo, J. _8INT3239 _9907 _gGenetic Resources Program |
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700 | 1 |
_aCrossa, J. _gGenetic Resources Program _8CCJL01 _959 |
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700 | 1 |
_aDzidzienyo, D. _916831 |
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700 | 1 |
_aBeyene, Y. _8INT2891 _9870 _gGlobal Maize Program |
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700 | 1 |
_aGowda, M. _8I1705963 _9795 _gGlobal Maize Program |
|
700 | 1 |
_aDreher, K.A. _8I1706147 _9808 _gGenetic Resources Program |
|
700 | 0 |
_aXuecai Zhang _gGlobal Maize Program _8INT3400 _9951 |
|
700 | 1 |
_aPrasanna, B.M. _gGlobal Maize Program _8INT3057 _9887 |
|
700 | 1 |
_aTongoona, P.B. _8001713456 _gFormerly Excellence in Breeding _9340 |
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700 | 1 |
_aDanquah, E. _96758 |
|
700 | 1 |
_aOlaoye, G. _92299 |
|
700 | 1 |
_aRobbins, K. _95987 |
|
773 | 0 |
_dBerlin (Germany) : Springer, 2021. _x0040-5752 _gv. 134, no. 1, p. 279-294 _tTheoretical and Applied Genetics _wu444762 |
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856 | 4 |
_yOpen Access through DSpace _uhttps://hdl.handle.net/10883/21003 |
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942 |
_cJA _n0 _2ddc |
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999 |
_c62827 _d62819 |