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J Med Genet 47:835-847 doi:10.1136/jmg.2010.078212
  • Original article

Ancestry informative markers for fine-scale individual assignment to worldwide populations

Editor's Choice
  1. Petros Drineas2
  1. 1Department of Molecular Biology and Genetics, Democritus University of Thrace, Alexandroupoli, Greece
  2. 2Department of Computer Science, Rensselaer Polytechnic Institute, Troy, New York, USA
  3. 3Computational Biology Group, IBM T.J. Watson Research Center, Yorktown Heights, New York, USA
  1. Correspondence to Dr Peristera Paschou, Department of Molecular Biology and Genetics, Democritus University of Thrace, Panepistimioupoli, Dragana, Ktirio 8, Alexandroupoli 68100, Greece; ppaschou{at}mbg.duth.gr
  • Received 18 February 2010
  • Revised 28 April 2010
  • Accepted 1 June 2010
  • Published Online First 4 October 2010

Abstract

Background and aims The analysis of large-scale genetic data from thousands of individuals has revealed the fact that subtle population genetic structure can be detected at levels that were previously unimaginable. Using the Human Genome Diversity Panel as reference (51 populations - 650,000 SNPs), this works describes a systematic evaluation of the resolution that can be achieved for the inference of genetic ancestry, even when small panels of genetic markers are used.

Methods and results A comprehensive investigation of human population structure around the world is undertaken by leveraging the power of Principal Components Analysis (PCA). The problem is dissected into hierarchical steps and a decision tree for the prediction of individual ancestry is proposed. A complete leave-one-out validation experiment demonstrates that, using all available SNPs, assignment of individuals to their self-reported populations of origin is essentially perfect. Ancestry informative genetic markers are selected using two different metrics (In and correlation with PCA scores). A thorough cross-validation experiment indicates that, in most cases here, the number of SNPs needed for ancestry inference can be successfully reduced to less than 0.1% of the original 650,000 while retaining close to 100% accuracy. This reduction can be achieved using a novel clustering-based redundancy removal algorithm that is also introduced here. Finally, the applicability of our suggested SNP panels is tested on HapMap Phase 3 populations.

Conclusion The proposed methods and ancestry informative marker panels, in combination with the increasingly more comprehensive databases of human genetic variation, open new horizons in a variety of fields, ranging from the study of human evolution and population history, to medical genetics and forensics.

Footnotes

  • Funding NSF, EMBO, Tourette Syndrome Association-USA.

  • Competing interests None.

  • Ethics approval This study was conducted with the approval of the RPI, Democritus University of Thrace.

  • Provenance and peer review Not commissioned; externally peer reviewed.