Using Whole-Genome Sequence Data to Predict Quantitative Trait Phenotypes in Drosophila melanogaster

2012 | journal article. A publication with affiliation to the University of Göttingen.

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​Using Whole-Genome Sequence Data to Predict Quantitative Trait Phenotypes in Drosophila melanogaster​
Ober, U.; Ayroles, J. F.; Stone, E. A.; Richards, S. J.; Zhu, D.; Gibbs, R. A. & Stricker, C. et al.​ (2012) 
PLoS Genetics8(5) art. e1002685​.​ DOI: https://doi.org/10.1371/journal.pgen.1002685 

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Authors
Ober, Ulrike; Ayroles, Julien F.; Stone, Eric A.; Richards, Stephen J.; Zhu, D.; Gibbs, Richard A.; Stricker, Christian; Gianola, Daniel S.; Schlather, Martin; Mackay, Trudy F. C.; Simianer, Henner
Abstract
Predicting organismal phenotypes from genotype data is important for plant and animal breeding, medicine, and evolutionary biology. Genomic-based phenotype prediction has been applied for single-nucleotide polymorphism (SNP) genotyping platforms, but not using complete genome sequences. Here, we report genomic prediction for starvation stress resistance and startle response in Drosophila melanogaster, using similar to 2.5 million SNPs determined by sequencing the Drosophila Genetic Reference Panel population of inbred lines. We constructed a genomic relationship matrix from the SNP data and used it in a genomic best linear unbiased prediction (GBLUP) model. We assessed predictive ability as the correlation between predicted genetic values and observed phenotypes by cross-validation, and found a predictive ability of 0.239 +/- 0.008 (0.230 +/- 0.012) for starvation resistance (startle response). The predictive ability of BayesB, a Bayesian method with internal SNP selection, was not greater than GBLUP. Selection of the 5% SNPs with either the highest absolute effect or variance explained did not improve predictive ability. Predictive ability decreased only when fewer than 150,000 SNPs were used to construct the genomic relationship matrix. We hypothesize that predictive power in this population stems from the SNP-based modeling of the subtle relationship structure caused by long-range linkage disequilibrium and not from population structure or SNPs in linkage disequilibrium with causal variants. We discuss the implications of these results for genomic prediction in other organisms.
Issue Date
2012
Status
published
Publisher
Public Library Science
Journal
PLoS Genetics 
ISSN
1553-7404
Sponsor
Open-Access-Publikationsfonds 2012

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