Fine-scale population structure and the era of next-generation sequencing

被引:24
作者
Henn, Brenna M. [1 ]
Gravel, Simon [1 ]
Moreno-Estrada, Andres [1 ]
Acevedo-Acevedo, Suehelay [2 ]
Bustamante, Carlos D. [1 ]
机构
[1] Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USA
[2] Univ Puerto Rico, Dept Biol, Mayaguez, PR USA
关键词
GENOME-WIDE PATTERNS; GENETIC-STRUCTURE; LACTASE-PERSISTENCE; NATURAL-SELECTION; HISTORY; ADAPTATION; ASSOCIATION; DIVERSITY; STRATIFICATION; SUBSTRUCTURE;
D O I
10.1093/hmg/ddq403
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Fine-scale population structure characterizes most continents and is especially pronounced in non-cosmopolitan populations. Roughly half of the world's population remains non-cosmopolitan and even populations within cities often assort along ethnic and linguistic categories. Barriers to random mating can be ecologically extreme, such as the Sahara Desert, or cultural, such as the Indian caste system. In either case, subpopulations accumulette genetic differences if the barrier is maintained over multiple generations. Genome-wide polymorphism data, initially with only a few hundred autosomal microsatellites, have clearly established differences in allele frequency not only among continental regions, but also within continents and within countries. We review recent evidence from the analysis of genome-wide polymorphism data for genetic boundaries delineating human population structure and the main demographic and genomic processes shaping variation, and discuss the implications of population structure for the distribution and discovery of disease-causing genetic variants, in the light of the imminent availability of sequencing data for a multitude of diverse human genomes.
引用
收藏
页码:R221 / R226
页数:6
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