Literature DB >> 23136122

Multiway admixture deconvolution using phased or unphased ancestral panels.

Claire Churchhouse1, Jonathan Marchini.   

Abstract

We describe a novel method for inferring the local ancestry of admixed individuals from dense genome-wide single nucleotide polymorphism data. The method, called MULTIMIX, allows multiple source populations, models population linkage disequilibrium between markers and is applicable to datasets in which the sample and source populations are either phased or unphased. The model is based upon a hidden Markov model of switches in ancestry between consecutive windows of loci. We model the observed haplotypes within each window using a multivariate normal distribution with parameters estimated from the ancestral panels. We present three methods to fit the model-Markov chain Monte Carlo sampling, the Expectation Maximization algorithm, and a Classification Expectation Maximization algorithm. The performance of our method on individuals simulated to be admixed with European and West African ancestry shows it to be comparable to HAPMIX, the ancestry calls of the two methods agreeing at 99.26% of loci across the three parameter groups. In addition to it being faster than HAPMIX, it is also found to perform well over a range of extent of admixture in a simulation involving three ancestral populations. In an analysis of real data, we estimate the contribution of European, West African and Native American ancestry to each locus in the Mexican samples of HapMap, giving estimates of ancestral proportions that are consistent with those previously reported.
© 2012 WILEY PERIODICALS, INC.

Mesh:

Year:  2012        PMID: 23136122     DOI: 10.1002/gepi.21692

Source DB:  PubMed          Journal:  Genet Epidemiol        ISSN: 0741-0395            Impact factor:   2.135


  30 in total

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2.  Mapping the human reference genome's missing sequence by three-way admixture in Latino genomes.

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4.  Leveraging ancestry to improve causal variant identification in exome sequencing for monogenic disorders.

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5.  A comprehensive survey of models for dissecting local ancestry deconvolution in human genome.

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6.  Eigenanalysis of SNP data with an identity by descent interpretation.

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9.  Local and global ancestry inference and applications to genetic association analysis for admixed populations.

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Journal:  Genet Epidemiol       Date:  2014-09       Impact factor: 2.135

10.  Origin of the PSEN1 E280A mutation causing early-onset Alzheimer's disease.

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