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

dc.contributor.authorOber, Ulrike
dc.contributor.authorAyroles, Julien F.
dc.contributor.authorStone, Eric
dc.contributor.authorRichards, Stephen
dc.contributor.authorZhu, Dianhui
dc.contributor.authorGibbs, R A
dc.contributor.authorStricker, Christian
dc.contributor.authorGianola, Daniel
dc.contributor.authorSchlather, Martin
dc.contributor.authorMackay, Trudy FC
dc.contributor.authorSimianer, Henner
dc.date.accessioned2018-11-29T22:55:34Z
dc.date.available2018-11-29T22:55:34Z
dc.date.issued2012
dc.date.updated2018-11-29T08:07:07Z
dc.description.abstractPredicting 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 ∼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.
dc.format.mimetypeapplication/pdfen_AU
dc.identifier.issn1553-7390
dc.identifier.urihttp://hdl.handle.net/1885/153204
dc.publisherPublic Library of Science
dc.sourcePLoS Genetics
dc.titleUsing Whole-Genome Sequence Data to Predict Quantitative Trait Phenotypes in Drosophila melanogaster
dc.typeJournal article
dcterms.accessRightsOpen Accessen_AU
local.bibliographicCitation.issue5
local.contributor.affiliationOber, Ulrike, Georg-August-Universität Göttingen
local.contributor.affiliationAyroles, Julien F., Harvard University
local.contributor.affiliationStone, Eric, College of Science, ANU
local.contributor.affiliationRichards, Stephen, Baylor College of Medicine
local.contributor.affiliationZhu, Dianhui, Baylor College of Medicine
local.contributor.affiliationGibbs, R A, Baylor College of Medicine
local.contributor.affiliationStricker, Christian, College of Health and Medicine, ANU
local.contributor.affiliationGianola, Daniel, University of Wisconsin–Madison
local.contributor.affiliationSchlather, Martin, University of Mannheim
local.contributor.affiliationMackay, Trudy FC, North Carolina State University
local.contributor.affiliationSimianer, Henner, Georg-August-Universität Göttingen
local.contributor.authoruidStone, Eric, u1019797
local.contributor.authoruidStricker, Christian, u4054348
local.description.notesImported from ARIES
local.identifier.absfor060408 - Genomics
local.identifier.absfor060412 - Quantitative Genetics (incl. Disease and Trait Mapping Genetics)
local.identifier.ariespublicationU3488905xPUB24794
local.identifier.citationvolume8
local.identifier.doi10.1371/journal.pgen.1002685
local.identifier.scopusID2-s2.0-84863652334
local.identifier.thomsonID000304864000017
local.type.statusPublished Version

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