Evaluating the accuracy of AIM panels at quantifying genome ancestry
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Abstract
Background
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.
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Bibliographic citation
Pardo-Seco, J., Martinón-Torres, F. & Salas, A. Evaluating the accuracy of AIM panels at quantifying genome ancestry. BMC Genomics 15, 543 (2014). https://doi.org/10.1186/1471-2164-15-543
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https://doi.org/10.1186/1471-2164-15-543Sponsors
The research leading to these results has received funding from the
“Ministerio de Ciencia e Innovación” (SAF2008-02971) and from the Plan
Galego IDT, Xunta de Galicia (EM 2012/045) (A.S.) and Consellería de
Sanidade/Xunta de Galicia (RHI07/2-intensificación actividad investigadora
and 10PXIB918184PR), Instituto Carlos III (Intensificación de la actividad
investigadora) and Fondo de Investigación Sanitaria (FIS; PI070069 and
PI1000540) del Plan Nacional de I + D + I and ‘fondos FEDER’ (F.M.T.), and the
grant from the Sistema Universitario Gallego- Modalidad REDES (2012-PG226)
of the Consellería de Cultura, Educación e Ordenación Universitaria of the
Xunta de Galicia (A.S., F.M.T.)
Rights
© 2014 Pardo-Seco et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated








