Modeling SNP array ascertainment with Approximate Bayesian Computation for demographic inference
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Final Published version
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Univ Arizona, Dept MathUniv Arizona, ARL Div Biotechnol
Issue Date
2018-07-05
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NATURE PUBLISHING GROUPCitation
Quinto-Cortés, C. D., Woerner, A. E., Watkins, J. C., & Hammer, M. F. (2018). Modeling SNP array ascertainment with Approximate Bayesian Computation for demographic inference. Scientific reports, 8(1), 10209; DOI:10.1038/s41598-018-28539-yJournal
SCIENTIFIC REPORTSRights
© The Author(s) 2018. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License.Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
Single nucleotide polymorphisms (SNPs) in commercial arrays have often been discovered in a small number of samples from selected populations. This ascertainment skews patterns of nucleotide diversity and affects population genetic inferences. We propose a demographic inference pipeline that explicitly models the SNP discovery protocol in an Approximate Bayesian Computation (ABC) framework. We simulated genomic regions according to a demographic model incorporating parameters for the divergence of three well-characterized HapMap populations and recreated the SNP distribution of a commercial array by varying the number of haploid samples and the allele frequency cut-off in the given regions. We then calculated summary statistics obtained from both the ascertained and genomic data and inferred ascertainment and demographic parameters. We implemented our pipeline to study the admixture process that gave rise to the present-day Mexican population. Our estimate of the time of admixture is closer to the historical dates than those in previous works which did not consider ascertainment bias. Although the use of whole genome sequences for demographic inference is becoming the norm, there are still underrepresented areas of the world from where only SNP array data are available. Our inference framework is applicable to those cases and will help with the demographic inference.Note
Open access journal.ISSN
2045-2322PubMed ID
29977040Version
Final published versionSponsors
CONACYT (National Council for Science and Technology, Mexico); Arizona Research Laboratories of the University of Arizona; Genetics Interdisciplinary Graduate Program of the University of ArizonaAdditional Links
http://www.nature.com/articles/s41598-018-28539-yae974a485f413a2113503eed53cd6c53
10.1038/s41598-018-28539-y
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Except where otherwise noted, this item's license is described as © The Author(s) 2018. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License.
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