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Modeling SNP array ascertainment with Approximate Bayesian Computation for demographic inference.
Quinto-Cortés, Consuelo D; Woerner, August E; Watkins, Joseph C; Hammer, Michael F.
Afiliación
  • Quinto-Cortés CD; National Laboratory of Genomics for Biodiversity (LANGEBIO), CINVESTAV, Irapuato, 36821, Mexico, Mexico. consuelo.quinto@cinvestav.mx.
  • Woerner AE; Center for Human Identification, University of North Texas Health Science Center, Texas, 76107, USA.
  • Watkins JC; Department of Mathematics, University of Arizona, Tucson, Arizona, 85721, USA.
  • Hammer MF; ARL Division of Biotechnology, University of Arizona, Tucson, Arizona, 85721, USA. mfh@email.arizona.edu.
Sci Rep ; 8(1): 10209, 2018 07 05.
Article en En | MEDLINE | ID: mdl-29977040
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.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Polimorfismo de Nucleótido Simple / Población Negra / Pueblo Asiatico / Población Blanca Tipo de estudio: Prognostic_studies País/Región como asunto: Africa / America do norte / Asia Idioma: En Revista: Sci Rep Año: 2018 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Polimorfismo de Nucleótido Simple / Población Negra / Pueblo Asiatico / Población Blanca Tipo de estudio: Prognostic_studies País/Región como asunto: Africa / America do norte / Asia Idioma: En Revista: Sci Rep Año: 2018 Tipo del documento: Article