gms | German Medical Science

65th Annual Meeting of the German Association for Medical Informatics, Biometry and Epidemiology (GMDS), Meeting of the Central European Network (CEN: German Region, Austro-Swiss Region and Polish Region) of the International Biometric Society (IBS)

06.09. - 09.09.2020, Berlin (online conference)

Optimizing the number of locations per sub-region in multi-environment trials

Meeting Abstract

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  • Maryna Prus - Otto von Guericke University of Magdeburg, FMA, IMST, Magdeburg, Germany
  • Hans-Peter Piepho - University of Hohenheim, Stuttgart, Germany

Deutsche Gesellschaft für Medizinische Informatik, Biometrie und Epidemiologie. 65th Annual Meeting of the German Association for Medical Informatics, Biometry and Epidemiology (GMDS), Meeting of the Central European Network (CEN: German Region, Austro-Swiss Region and Polish Region) of the International Biometric Society (IBS). Berlin, 06.-09.09.2020. Düsseldorf: German Medical Science GMS Publishing House; 2021. DocAbstr. 37

doi: 10.3205/20gmds001, urn:nbn:de:0183-20gmds0012

Veröffentlicht: 26. Februar 2021

© 2021 Prus et al.
Dieser Artikel ist ein Open-Access-Artikel und steht unter den Lizenzbedingungen der Creative Commons Attribution 4.0 License (Namensnennung). Lizenz-Angaben siehe http://creativecommons.org/licenses/by/4.0/.


Gliederung

Text

New crop varieties are usually evaluated for their performance in a target population of environments (TPE). This evaluation requires conducting randomized field trials at several environments sampled from the TPE. Such trials are called multi-environment trials (MET).

If the TPE is large and can be suitably stratified along geographical borders or agro-ecological zonations, it may be advantageous to subdivide the TPE into sub-regions. If the same set of genotypes is tested at a number of locations in each of the sub-regions, a linear mixed model may be fitted with random genotype-within-sub-region effects that allows estimating a genotype's average performance in each sub-region using best linear unbiased prediction.

The design of MET for a sub-divided TPE involves two decisions: (1) The total number of environments at which to conduct the trials and (2) the allocation of this total number of environments to the different sub-regions. The present work is devoted to the second decision: We propose an analytical approach for computation of optimal allocation numbers per sub-region with respect to the prediction of the genotype effects.

The authors declare that they have no competing interests.

The authors declare that an ethics committee vote is not required.