Literature DB >> 30459280

Local PCA Shows How the Effect of Population Structure Differs Along the Genome.

Han Li1, Peter Ralph2,3,4.   

Abstract

Population structure leads to systematic patterns in measures of mean relatedness between individuals in large genomic data sets, which are often discovered and visualized using dimension reduction techniques such as principal component analysis (PCA). Mean relatedness is an average of the relationships across locus-specific genealogical trees, which can be strongly affected on intermediate genomic scales by linked selection and other factors. We show how to use local PCA to describe this intermediate-scale heterogeneity in patterns of relatedness, and apply the method to genomic data from three species, finding in each that the effect of population structure can vary substantially across only a few megabases. In a global human data set, localized heterogeneity is likely explained by polymorphic chromosomal inversions. In a range-wide data set of Medicago truncatula, factors that produce heterogeneity are shared between chromosomes, correlate with local gene density, and may be caused by linked selection, such as background selection or local adaptation. In a data set of primarily African Drosophila melanogaster, large-scale heterogeneity across each chromosome arm is explained by known chromosomal inversions thought to be under recent selection and, after removing samples carrying inversions, remaining heterogeneity is correlated with recombination rate and gene density, again suggesting a role for linked selection. The visualization method provides a flexible new way to discover biological drivers of genetic variation, and its application to data highlights the strong effects that linked selection and chromosomal inversions can have on observed patterns of genetic variation.
Copyright © 2019 by the Genetics Society of America.

Entities:  

Keywords:  genomic landscape; local PCA; population structure; visualization

Mesh:

Year:  2018        PMID: 30459280      PMCID: PMC6325702          DOI: 10.1534/genetics.118.301747

Source DB:  PubMed          Journal:  Genetics        ISSN: 0016-6731            Impact factor:   4.562


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