Inferring admixture histories of human populations using linkage disequilibrium.

Abstract:

:Long-range migrations and the resulting admixtures between populations have been important forces shaping human genetic diversity. Most existing methods for detecting and reconstructing historical admixture events are based on allele frequency divergences or patterns of ancestry segments in chromosomes of admixed individuals. An emerging new approach harnesses the exponential decay of admixture-induced linkage disequilibrium (LD) as a function of genetic distance. Here, we comprehensively develop LD-based inference into a versatile tool for investigating admixture. We present a new weighted LD statistic that can be used to infer mixture proportions as well as dates with fewer constraints on reference populations than previous methods. We define an LD-based three-population test for admixture and identify scenarios in which it can detect admixture events that previous formal tests cannot. We further show that we can uncover phylogenetic relationships among populations by comparing weighted LD curves obtained using a suite of references. Finally, we describe several improvements to the computation and fitting of weighted LD curves that greatly increase the robustness and speed of the calculations. We implement all of these advances in a software package, ALDER, which we validate in simulations and apply to test for admixture among all populations from the Human Genome Diversity Project (HGDP), highlighting insights into the admixture history of Central African Pygmies, Sardinians, and Japanese.

journal_name

Genetics

journal_title

Genetics

authors

Loh PR,Lipson M,Patterson N,Moorjani P,Pickrell JK,Reich D,Berger B

doi

10.1534/genetics.112.147330

subject

Has Abstract

pub_date

2013-04-01 00:00:00

pages

1233-54

issue

4

eissn

0016-6731

issn

1943-2631

pii

genetics.112.147330

journal_volume

193

pub_type

杂志文章

相关文献

GENETICS文献大全
  • Allelic diversification at the C (OsC1) locus of wild and cultivated rice: nucleotide changes associated with phenotypes.

    abstract::Divergent phenotypes are often detected in domesticated plants despite the existence of invariant phenotypes in their wild forms. One such example in rice is the occurrence of varying degrees of apiculus coloration due to anthocyanin pigmentation, which was previously reported to be caused by a series of alleles at th...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.103.018390

    authors: Saitoh K,Onishi K,Mikami I,Thidar K,Sano Y

    更新日期:2004-10-01 00:00:00

  • Maximum likelihood estimation of population parameters.

    abstract::One of the most important parameters in population genetics is theta = 4Ne mu where Ne is the effective population size and mu is the rate of mutation per gene per generation. We study two related problems, using the maximum likelihood method and the theory of coalescence. One problem is the potential improvement of a...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Fu YX,Li WH

    更新日期:1993-08-01 00:00:00

  • High-throughput computer vision introduces the time axis to a quantitative trait map of a plant growth response.

    abstract::Automated image acquisition, a custom analysis algorithm, and a distributed computing resource were used to add time as a third dimension to a quantitative trait locus (QTL) map for plant root gravitropism, a model growth response to an environmental cue. Digital images of Arabidopsis thaliana seedling roots from two ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.113.153346

    authors: Moore CR,Johnson LS,Kwak IY,Livny M,Broman KW,Spalding EP

    更新日期:2013-11-01 00:00:00

  • Persistence time of loss-of-function mutations at nonessential loci affecting eye color in Drosophila melanogaster.

    abstract::Persistence time of a mutant allele, the expected number of generations before its elimination from the population, can be estimated as the ratio of the number of segregating mutations per individual over the mutation rate per generation. We screened two natural populations of Drosophila melanogaster for mutations cau...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.105.046094

    authors: Yampolsky LY,Allen C,Shabalina SA,Kondrashov AS

    更新日期:2005-12-01 00:00:00

  • On the effect of fluctuating recombination rates on the decorrelation of gene histories in the human genome.

    abstract::We show how to incorporate fluctuations of the recombination rate along the chromosome into standard gene-genealogical models for the decorrelation of gene histories. This enables us to determine how small-scale fluctuations (Poissonian hot-spot model) and large-scale variations (Kong et al. 2002) of the recombination...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.103.018002

    authors: Eriksson A,Mehlig B

    更新日期:2005-02-01 00:00:00

  • Amino acid replacements resulting from suppression and missense reversion of a chain-terminator mutation in Neurospora.

    abstract::The Neurospora crassa super-suppressor mutation, ssu-1, suppresses the auxotrophic phenotype of the mutant am(17) by inserting tyrosine at residue 313 of NADP-specific glutamate dehydrogenase, a position occupied in the wild type by glutamate. Two classes of am(17) revertants due to further mutation within the am gene...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Seale TW,Brett M,Baron AJ,Fincham JR

    更新日期:1977-06-01 00:00:00

  • A method for inferring the rate of occurrence and fitness effects of advantageous mutations.

    abstract::The distribution of fitness effects (DFE) of new mutations is of fundamental importance in evolutionary genetics. Recently, methods have been developed for inferring the DFE that use information from the allele frequency distributions of putatively neutral and selected nucleotide polymorphic variants in a population s...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.111.131730

    authors: Schneider A,Charlesworth B,Eyre-Walker A,Keightley PD

    更新日期:2011-12-01 00:00:00

  • Haplotype probabilities for multiple-strain recombinant inbred lines.

    abstract::Recombinant inbred lines (RIL) derived from multiple inbred strains can serve as a powerful resource for the genetic dissection of complex traits. The use of such multiple-strain RIL requires a detailed knowledge of the haplotype structure in such lines. Broman (2005) derived the two- and three-point haplotype probabi...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.106.064063

    authors: Teuscher F,Broman KW

    更新日期:2007-03-01 00:00:00

  • Best Prediction of the Additive Genomic Variance in Random-Effects Models.

    abstract::The additive genomic variance in linear models with random marker effects can be defined as a random variable that is in accordance with classical quantitative genetics theory. Common approaches to estimate the genomic variance in random-effects linear models based on genomic marker data can be regarded as estimating ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.119.302324

    authors: Schreck N,Piepho HP,Schlather M

    更新日期:2019-10-01 00:00:00

  • Marker-dependent recombination in T4 bacteriophage. III. Structural prerequisites for marker discrimination.

    abstract::Distance- as well as marker-dependence of genetic recombination of bacteriophage T4 was studied in crosses between rIIB mutants with known base sequences. The notion of a "basic recombination," which is the recombination within distances shorter than hybrid DNA length in the absence of mismatch repair and any marker e...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Shcherbakov VP,Plugina LA

    更新日期:1991-08-01 00:00:00

  • Molecular population genetics and evolution of a prion-like protein in Saccharomyces cerevisiae.

    abstract::The prion-like behavior of Sup35p, the eRF3 homolog in the yeast Saccharomyces cerevisiae, mediates the activity of the cytoplasmic nonsense suppressor known as [PSI(+)]. Sup35p is divided into three regions of distinct function. The N-terminal and middle (M) regions are required for the induction and propagation of [...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Jensen MA,True HL,Chernoff YO,Lindquist S

    更新日期:2001-10-01 00:00:00

  • High intake of dietary sugar enhances bisphenol A (BPA) disruption and reveals ribosome-mediated pathways of toxicity.

    abstract::Bisphenol A (BPA) is an organic compound to which human populations are ubiquitously exposed. Epidemiological data suggest BPA exposure might be associated with higher rates of diabetes and reproductive anomalies. Health concerns also include transgenerational consequences, but these mechanisms are crudely defined. Si...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.114.163170

    authors: Branco AT,Lemos B

    更新日期:2014-05-01 00:00:00

  • Analysis of dominant mutations affecting muscle excitation in Caenorhabditis elegans.

    abstract::We examined mutations that disrupt muscle activation in Caenorhabditis elegans. Fifteen of 17 of these genes were identified previously and we describe new mutations in three of them. We also describe mutations in two new genes, exp-3 and exp-4. We assessed the degree of defect in pharyngeal, body-wall, egg-laying, an...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Reiner DJ,Weinshenker D,Thomas JH

    更新日期:1995-11-01 00:00:00

  • The Drosophila melanogaster Suppressor of deltex gene, a regulator of the Notch receptor signaling pathway, is an E3 class ubiquitin ligase.

    abstract::During development, the Notch receptor regulates many cell fate decisions by a signaling pathway that has been conserved during evolution. One positive regulator of Notch is Deltex, a cytoplasmic, zinc finger domain protein, which binds to the intracellular domain of Notch. Phenotypes resulting from mutations in delte...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Cornell M,Evans DA,Mann R,Fostier M,Flasza M,Monthatong M,Artavanis-Tsakonas S,Baron M

    更新日期:1999-06-01 00:00:00

  • Multiple origins of cytologically identical chromosome inversions in the Anopheles gambiae complex.

    abstract::For more than 60 years, evolutionary cytogeneticists have been using naturally occurring chromosomal inversions to infer phylogenetic histories, especially in insects with polytene chromosomes. The validity of this method is predicated on the assumption that inversions arise only once in the history of a lineage, so t...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Caccone A,Min GS,Powell JR

    更新日期:1998-10-01 00:00:00

  • Evidence for parallel processing of sensory information controlling dauer formation in Caenorhabditis elegans.

    abstract::Dauer formation in Caenorhabditis elegans is induced by chemosensation of high levels of a constitutively secreted pheromone. Seven genes defined by mutations that confer a dauer-formation constitutive phenotype (Daf-c) can be congruently divided into two groups by any of three criteria. Group 1 genes (daf-11 and daf-...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Thomas JH,Birnby DA,Vowels JJ

    更新日期:1993-08-01 00:00:00

  • The contribution of the Y chromosome to hybrid male sterility in house mice.

    abstract::Hybrid sterility in the heterogametic sex is a common feature of speciation in animals. In house mice, the contribution of the Mus musculus musculus X chromosome to hybrid male sterility is large. It is not known, however, whether F1 male sterility is caused by X-Y or X-autosome incompatibilities or a combination of b...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.112.141804

    authors: Campbell P,Good JM,Dean MD,Tucker PK,Nachman MW

    更新日期:2012-08-01 00:00:00

  • A fine structure map of the salmonella histidine operator-promoter.

    abstract::Over 100 regulatory mutations linked to the histidine (his) operon of S. typhimurium have been isolated. They all map in a region estimated to be several hundred base pairs in length located at one end of the his operon ("the hisO region"). The mutations are located at sixteen recombinationally separable sites or are ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Ely B,Fankhauser DB,Hartman PE

    更新日期:1974-10-01 00:00:00

  • Epistasis in monkeyflowers.

    abstract::Epistasis contributes significantly to intrapopulation variation in floral morphology, development time, and male fitness components of Mimulus guttatus. This is demonstrated with a replicated line-cross experiment involving slightly over 7000 plants. The line-cross methodology is based on estimates for means. It thus...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.105.041525

    authors: Kelly JK

    更新日期:2005-12-01 00:00:00

  • A selfish gene governing pollen-pistil compatibility confers reproductive isolation between maize relatives.

    abstract::Some populations of maize's closest relatives, the annual teosintes of Mexico, are unreceptive to maize pollen. When present in the pistil (silk and ovary) a number of maize genes discriminate against or exclude pollen not carrying the same allele. An analogous gene Tcb1-s was found in some teosinte populations but no...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.105.048645

    authors: Kermicle JL

    更新日期:2006-01-01 00:00:00

  • An AFLP-based genetic linkage map of channel catfish (Ictalurus punctatus) constructed by using an interspecific hybrid resource family.

    abstract::Catfish is the major aquaculture species in the United States. The hybrid catfish produced by crossing channel catfish females with blue catfish males exhibit a number of desirable production traits, but their mass production has been difficult. To introduce desirable genes from blue catfish into channel catfish throu...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Liu Z,Karsi A,Li P,Cao D,Dunham R

    更新日期:2003-10-01 00:00:00

  • Genomic Structure of Hstx2 Modifier of Prdm9-Dependent Hybrid Male Sterility in Mice.

    abstract::F1 hybrids between mouse inbred strains PWD and C57BL/6 represent the most thoroughly genetically defined model of hybrid sterility in vertebrates. Hybrid male sterility can be fully reconstituted from three components of this model, the Prdm9 gene, intersubspecific homeology of Mus musculus musculus and Mus musculus ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.119.302554

    authors: Lustyk D,Kinský S,Ullrich KK,Yancoskie M,Kašíková L,Gergelits V,Sedlacek R,Chan YF,Odenthal-Hesse L,Forejt J,Jansa P

    更新日期:2019-11-01 00:00:00

  • Genetics of glucocorticoid receptor levels in recombinant inbred lines of mice.

    abstract::Hepatic glucocorticoid receptor binding activity was measured in A/J, C57BL/6J, their F1 reciprocal crosses and their F1 recombinant inbred (RI) lines. The glucocorticoid binding capacity was measured in Hepes buffer and Hepes buffer plus dithiothreitol (DTT). The A/J parental strain showed higher levels, and a greate...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Liu SL,Erickson RP

    更新日期:1986-07-01 00:00:00

  • hairy: A quantitative trait locus for drosophila sensory bristle number.

    abstract::Advances in medicine, agriculture, and an understanding of evolution depend on resolving the genetic architecture of quantitative traits, which is challenging since variation for complex traits is caused by multiple interacting quantitative trait loci (QTL) with small and conditional effects. Here, we show that the ke...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Robin C,Lyman RF,Long AD,Langley CH,Mackay TF

    更新日期:2002-09-01 00:00:00

  • Evidence that the pre-mRNA splicing factor Clf1p plays a role in DNA replication in Saccharomyces cerevisiae.

    abstract::Clf1p is an essential, highly conserved protein in S. cerevisiae that has been implicated in pre-mRNA splicing. Clf1p's ortholog in Drosophila, Crn, is required for normal cell proliferation. Cells depleted of Clf1p arrest primarily with large buds, a single nucleus, a 2C DNA content, and a short, intact mitotic spind...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Zhu W,Rainville IR,Ding M,Bolus M,Heintz NH,Pederson DS

    更新日期:2002-04-01 00:00:00

  • A genetic map of quantitative trait loci for body weight in the mouse.

    abstract::The genetic basis of body weight in the mouse was investigated by measuring frequency changes of microsatellite marker alleles in lines divergently selected for body weight from a base population of a cross between two inbred strains. In several regions of the genome, sharp peaks of frequency change at linked markers ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Keightley PD,Hardge T,May L,Bulfield G

    更新日期:1996-01-01 00:00:00

  • The evolution of isochores: evidence from SNP frequency distributions.

    abstract::The large-scale systematic variation in nucleotide composition along mammalian and avian genomes has been a focus of the debate between neutralist and selectionist views of molecular evolution. Here we test whether the compositional variation is due to mutation bias using two new tests, which do not assume composition...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Lercher MJ,Smith NG,Eyre-Walker A,Hurst LD

    更新日期:2002-12-01 00:00:00

  • Polymorphism and locus-specific effects on polymorphism at microsatellite loci in natural Drosophila melanogaster populations.

    abstract::We have studied the natural variation at microsatellite loci in two African and five non-African populations of Drosophila melanogaster. Ten dinucleotide simple sequence loci were cloned from chromosomally mapped P1 clones and typed for single individuals from isofemale lines of the respective populations. We find tha...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Schlötterer C,Vogl C,Tautz D

    更新日期:1997-05-01 00:00:00

  • Genetic instability within monotonous runs of CpG sequences in Escherichia coli.

    abstract::Genetic information can be altered by base substitutions, frameshift mutations, and addition or deletion of nucleotides. Deletions represent an important class of genetic aberration occurring at DNA sequences where it is often possible to predict the existence of intermediates of mutation. Instability within tracts of...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Bichara M,Schumacher S,Fuchs RP

    更新日期:1995-07-01 00:00:00

  • Four chromo-domain proteins of Schizosaccharomyces pombe differentially repress transcription at various chromosomal locations.

    abstract::Transcription is repressed in regions of the fission yeast genome close to centromeres, telomeres, or the silent mating-type cassettes mat2-P and mat3-M. The repression involves the chromo-domain proteins Swi6 and Clr4. We report that two other chromo-domain proteins, Chp1 and Chp2, are also important for these positi...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Thon G,Verhein-Hansen J

    更新日期:2000-06-01 00:00:00