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dc.contributor.authorPardo Seco, Jacobo José
dc.contributor.authorSalas Ellacuriaga, Antonio
dc.contributor.authorMartinón Torres, Federico 
dc.date.accessioned2017-06-07T07:22:25Z
dc.date.available2017-06-07T07:22:25Z
dc.date.issued2014
dc.identifier.issn1471-2164
dc.identifier.urihttp://hdl.handle.net/20.500.11940/5677
dc.description.abstractBackground: There is a growing interest among geneticists in developing panels of Ancestry Informative Markers (AIMs) aimed at measuring the biogeographical ancestry of individual genomes. The efficiency of these panels is commonly tested empirically by contrasting self-reported ancestry with the ancestry estimated from these panels. Results: Using SNP data from HapMap we carried out a simulation-based study aimed at measuring the effect of SNP coverage on the estimation of genome ancestry. For three of the main continental groups (Africans, East Asians, Europeans) ancestry was first estimated using the whole HapMap SNP database as a proxy for global genome ancestry; these estimates were subsequently compared to those obtained from pre-designed AIM panels. Panels that consider >400 AIMs capture genome ancestry reasonably well, while those containing a few dozen AIMs show a large variability in ancestry estimates. Curiously, 500-1,000 SNPs selected at random from the genome provide an unbiased estimate of genome ancestry and perform as well as any AIM panel of similar size. In simulated scenarios of population admixture, panels containing few AIMs also show important deficiencies to measure genome ancestry. Conclusions: The results indicate that the ability to estimate genome ancestry is strongly dependent on the number of AIMs used, and not primarily on their individual informativeness. Caution should be taken when making individual (medical, forensic, or anthropological) inferences based on AIMs.
dc.language.isoeng
dc.rightsAtribución 4.0 Internacional
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subject.meshGenome, Human
dc.subject.meshGenotyping Techniques
dc.subject.meshHapMap Project
dc.subject.meshGenotyping Techniques
dc.subject.meshPolymorphism, Single Nucleotide
dc.subject.meshPrincipal Component Analysis
dc.titleEvaluating the accuracy of AIM panels at quantifying genome ancestry
dc.typeArtigoes
dc.authorsophosPardo-Seco, J.
dc.authorsophosMartinón-Torres, F.
dc.authorsophosSalas, A.
dc.identifier.doi10.1186/1471-2164-15-543
dc.identifier.isi338892700001
dc.identifier.pmid24981136
dc.identifier.sophos14908
dc.journal.titleBMC GENOMICS
dc.organizationConsellería de Sanidade::Fundación pública Galega de Medicina Xenómica
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Santiago - Complexo Hospitalario Universitario de Santiago::Pediatría
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Santiago::IDIS.- Instituto de investigaciones sanitarias de Santiago
dc.page.initial543
dc.rights.accessRightsopenAccess
dc.subject.decsGenoma Humano
dc.subject.decsTécnicas de Genotipaje
dc.subject.decsProyecto Mapa de Haplotipos
dc.subject.decsTécnicas de Genotipaje
dc.subject.decsPolimorfismo de Nucleótido Simple
dc.subject.decsAnálisis de Componente Principal
dc.typesophosArtículo Original
dc.volume.number15


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