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      Needles: Toward Large-Scale Genomic Prediction with Marker-by-Environment Interaction

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          Abstract

          Genomic prediction relies on genotypic marker information to predict the agronomic performance of future hybrid breeds based on trial records. Because the effect of markers may vary substantially under the influence of different environmental conditions, marker-by-environment interaction effects have to be taken into account. However, this may lead to a dramatic increase in the computational resources needed for analyzing large-scale trial data. A high-performance computing solution, called Needles, is presented for handling such data sets. Needles is tailored to the particular properties of the underlying algebraic framework by exploiting a sparse matrix formalism where suited and by utilizing distributed computing techniques to enable the use of a dedicated computing cluster. It is demonstrated that large-scale analyses can be performed within reasonable time frames with this framework. Moreover, by analyzing simulated trial data, it is shown that the effects of markers with a high environmental interaction can be predicted more accurately when more records per environment are available in the training data. The availability of such data and their analysis with Needles also may lead to the discovery of highly contributing QTL in specific environmental conditions. Such a framework thus opens the path for plant breeders to select crops based on these QTL, resulting in hybrid lines with optimized agronomic performance in specific environmental conditions.

          Author and article information

          Journal
          Genetics
          Genetics
          genetics
          genetics
          genetics
          Genetics
          Genetics Society of America
          0016-6731
          1943-2631
          May 2016
          29 February 2016
          : 203
          : 1
          : 543-555
          Affiliations
          [* ]KERMIT, Department of Mathematical Modelling, Statistics and Bioinformatics, Ghent University, B-9000 Ghent, Belgium
          []Bioinformatics Institute Ghent, Ghent University, B-9000 Ghent, Belgium
          []Institute of Computational Science, Università della Svizzera italiana, CH-6904 Lugano, Switzerland
          [§ ]Progeno, B-9052 Zwijnaarde, Belgium
          [** ]Department of Information Technology (INTEC), Ghent University–iMinds, B-9000 Ghent, Belgium
          Author notes
          [1 ]Corresponding author: KERMIT, Department of Mathematical Modelling, Statistics and Bioinformatics, Faculty of Bioscience Engineering, Ghent University, Coupure Links 653, B-9000 Ghent, Belgium. E-mail: arne.deconinck@ 123456ugent.be
          Author information
          http://orcid.org/0000-0002-3876-620X
          http://orcid.org/0000-0002-9994-8269
          Article
          PMC4858798 PMC4858798 4858798 179887
          10.1534/genetics.115.179887
          4858798
          26936924
          2b336bf2-2b30-40f4-a4c9-d280da0ba9c0
          Copyright © 2016 by the Genetics Society of America
          History
          : 26 June 2015
          : 25 January 2016
          Page count
          Figures: 4, Tables: 3, Equations: 19, References: 51, Pages: 13
          Categories
          Investigations
          Genomic Selection

          simulated data,GenPred,shared data resource,genomic selection,genomic prediction,marker-by-environment interaction,high-performance computing,variance component estimation

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