Abstract
Population structure is a confounding factor in Genome Wide Association Studies, increasing the rate of false positive associations. In order to correct for it, several model-based algorithms such as ADMIXTURE and STRUCTURE have been proposed. These tend to suffer from the fact that they have a considerable computational burden, limiting their applicability when used with large datasets, such as those produced by Next Generation Sequencing (NGS) techniques. To address this, non-model based approaches such as SNMF and EIGENSTRAT have been proposed, which scale better with larger data. Here we present a novel non-model based approach, PSIKO, which is based on a unique combination of linear kernel-PCA and least-squares optimization and allows for the inference of admixture coefficients, principal components, and number of founder populations of a dataset. PSIKO has been compared against existing leading methods on a variety of simulation scenarios, as well as on real biological data. We found that in addition to producing results of the same quality as other tested methods, PSIKO scales extremely well with dataset size, being considerably (up to 30 times) faster for longer sequences than even state of the art methods such as SNMF. PSIKO and accompanying manual are freely available at https://www.uea.ac.uk/computing/psiko.
Original language | English |
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Pages (from-to) | 1421-31 |
Number of pages | 11 |
Journal | Genetics |
Volume | 198 |
Issue number | 4 |
Early online date | 16 Oct 2014 |
DOIs | |
Publication status | Published - Dec 2014 |
Keywords
- Q-matrix
- Genome-Wide Association Studies
- admixture inference
- kernel-PCA
- population structure
Profiles
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Katharina Huber
- School of Computing Sciences - Associate Professor
- Computational Biology - Member
Person: Research Group Member, Academic, Teaching & Research