The power of single-nucleotide polymorphisms for large-scale parentage inference.

Abstract:

:Likelihood-based parentage inference depends on the distribution of a likelihood-ratio statistic, which, in most cases of interest, cannot be exactly determined, but only approximated by Monte Carlo simulation. We provide importance-sampling algorithms for efficiently approximating very small tail probabilities in the distribution of the likelihood-ratio statistic. These importance-sampling methods allow the estimation of small false-positive rates and hence permit likelihood-based inference of parentage in large studies involving a great number of potential parents and many potential offspring. We investigate the performance of these importance-sampling algorithms in the context of parentage inference using single-nucleotide polymorphism (SNP) data and find that they may accelerate the computation of tail probabilities >1 millionfold. We subsequently use the importance-sampling algorithms to calculate the power available with SNPs for large-scale parentage studies, paying particular attention to the effect of genotyping errors and the occurrence of related individuals among the members of the putative mother-father-offspring trios. These simulations show that 60-100 SNPs may allow accurate pedigree reconstruction, even in situations involving thousands of potential mothers, fathers, and offspring. In addition, we compare the power of exclusion-based parentage inference to that of the likelihood-based method. Likelihood-based inference is much more powerful under many conditions; exclusion-based inference would require 40% more SNP loci to achieve the same accuracy as the likelihood-based approach in one common scenario. Our results demonstrate that SNPs are a powerful tool for parentage inference in large managed and/or natural populations.

journal_name

Genetics

journal_title

Genetics

authors

Anderson EC,Garza JC

doi

10.1534/genetics.105.048074

keywords:

subject

Has Abstract

pub_date

2006-04-01 00:00:00

pages

2567-82

issue

4

eissn

0016-6731

issn

1943-2631

pii

genetics.105.048074

journal_volume

172

pub_type

杂志文章

相关文献

GENETICS文献大全
  • Age-specific properties of spontaneous mutations affecting mortality in Drosophila melanogaster.

    abstract::An analysis of the effects of spontaneous mutations affecting age-specific mortality was conducted using 29 lines of Drosophila melanogaster that had accumulated spontaneous mutations for 19 generations. Divergence among the lines was used to estimate the mutational variance for weekly mortality rates and the covarian...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Pletcher SD,Houle D,Curtsinger JW

    更新日期:1998-01-01 00:00:00

  • The rate of adaptation in large sexual populations with linear chromosomes.

    abstract::In large populations, multiple beneficial mutations may be simultaneously spreading. In asexual populations, these mutations must either arise on the same background or compete against each other. In sexual populations, recombination can bring together beneficial alleles from different backgrounds, but tightly linked ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.113.160705

    authors: Weissman DB,Hallatschek O

    更新日期:2014-04-01 00:00:00

  • Mitotic chromosome transmission fidelity mutants in Saccharomyces cerevisiae.

    abstract::We have isolated 136 independent mutations in haploid yeast strains that exhibit decreased chromosome transmission fidelity in mitosis. Eighty-five percent of the mutations are recessive and 15% are partially dominant. Complementation analysis between MATa and MAT alpha isolates identifies 11 chromosome transmission f...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Spencer F,Gerring SL,Connelly C,Hieter P

    更新日期:1990-02-01 00:00:00

  • Restructuring of Holocentric Centromeres During Meiosis in the Plant Rhynchospora pubera.

    abstract::Centromeres are responsible for the correct segregation of chromosomes during mitosis and meiosis. Holocentric chromosomes, characterized by multiple centromere units along each chromatid, have particular adaptations to ensure regular disjunction during meiosis. Here we show by detecting CENH3, CENP-C, tubulin, and ce...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.116.191213

    authors: Marques A,Schubert V,Houben A,Pedrosa-Harand A

    更新日期:2016-10-01 00:00:00

  • Antisense Transcription of Retrotransposons in Drosophila: An Origin of Endogenous Small Interfering RNA Precursors.

    abstract::Movement of transposons causes insertions, deletions, and chromosomal rearrangements potentially leading to premature lethality in Drosophila melanogaster. To repress these elements and combat genomic instability, eukaryotes have evolved several small RNA-mediated defense mechanisms. Specifically, in Drosophila somati...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.115.177196

    authors: Russo J,Harrington AW,Steiniger M

    更新日期:2016-01-01 00:00:00

  • Partial selfing and linkage: the effect of a heterotic locus on a neutral locus.

    abstract::Equilibria are determined for the two-locus model in a partially selfing population when one locus is neutral and the other locus is heterotic. At an equilibrium point, the frequency of heterozygotes at the neutral locus is greater than that expected from one-locus theory, even if the heterotic locus is on a different...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Strobeck C

    更新日期:1979-05-01 00:00:00

  • Insights into three whole-genome duplications gleaned from the Paramecium caudatum genome sequence.

    abstract::Paramecium has long been a model eukaryote. The sequence of the Paramecium tetraurelia genome reveals a history of three successive whole-genome duplications (WGDs), and the sequences of P. biaurelia and P. sexaurelia suggest that these WGDs are shared by all members of the aurelia species complex. Here, we present th...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.114.163287

    authors: McGrath CL,Gout JF,Doak TG,Yanagi A,Lynch M

    更新日期:2014-08-01 00:00:00

  • Estimating levels of gene flow in natural populations.

    abstract::The results from a simulation model of selection, mutation and genetic drift in a geographically subdivided population are presented. The infinite-alleles mutation model of Kimura and Crow (1964) is asumed, and both advantageous and deleterious mutations are considered. It is shown that the average frequency of an all...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Slatkin M

    更新日期:1981-10-01 00:00:00

  • Length variation, heteroplasmy and sequence divergence in the mitochondrial DNA of four species of sturgeon (Acipenser).

    abstract::The extent of mtDNA length variation and heteroplasmy as well as DNA sequences of the control region and two tRNA genes were determined for four North American sturgeon species: Acipenser transmontanus, A. medirostris, A. fulvescens and A. oxyrhnychus. Across the Continental Divide, a division in the occurrence of len...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Brown JR,Beckenbach K,Beckenbach AT,Smith MJ

    更新日期:1996-02-01 00:00:00

  • DAF-16-dependent suppression of immunity during reproduction in Caenorhabditis elegans.

    abstract::To further understand how the nematode Caenorhabditis elegans defends itself against pathogen attack, we analyzed enhanced pathogen resistance (epr) mutants obtained from a forward genetic screen. We also examined several well-characterized sterile mutants that exhibit an Epr phenotype. We found that sterility and pat...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.107.083923

    authors: Miyata S,Begun J,Troemel ER,Ausubel FM

    更新日期:2008-02-01 00:00:00

  • The genes for mouse salivary androgen-binding protein (ABP) subunits alpha and gamma are located on chromosome 7.

    abstract::We demonstrate that the previously described gene Androgen binding protein (Abp; Dlouhy and Karn, 1984) codes for the Alpha subunit of ABP and rename the locus Androgen binding protein alpha (Abpa). A study of recombinant inbred strains demonstrates that Abpa is located on chromosome 7 near Glucose phosphate isomerase...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Dlouhy SR,Taylor BA,Karn RC

    更新日期:1987-03-01 00:00:00

  • Nonsense motility mutants in Salmonella typhimurium.

    abstract::Of 313 motility-deficient mutants isolated from an LT2 his(amber) strain fixed in phase 1 by gene vh2(-), 25 regained motility when amber or ochre suppressors were introduced, in F' factors or by transduction. The fla mutants (23 amber, 1 ochre) fell in complementation groups A, B, C, F, K, a new group, M, and at leas...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Vary PS,Stocker BA

    更新日期:1973-02-01 00:00:00

  • Identification of genes that promote or inhibit olfactory memory formation in Drosophila.

    abstract::Genetic screens in Drosophila melanogaster and other organisms have been pursued to filter the genome for genetic functions important for memory formation. Such screens have employed primarily chemical or transposon-mediated mutagenesis and have identified numerous mutants including classical memory mutants, dunce and...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.114.173575

    authors: Walkinshaw E,Gai Y,Farkas C,Richter D,Nicholas E,Keleman K,Davis RL

    更新日期:2015-04-01 00:00:00

  • Genetic modulation of RNA metabolism in Drosophila. IV. Measurement of rats of RNA synthesis by density labeling.

    abstract::Accumulation of RNA was measured in adult males of two genotypes: car bb/Ybb- and car bb/YbbSuVar-5. The two genotypes have similar amounts of rDNA, which is reduced in comparison to wild type (CLARK, STRAUSBAUGH and KIEFER 1977). Although genotypically bobbed, car bb/YbbSuVar-5 flies have a wild-type phenotype; car b...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Strausbaugh LD,Clark SH,Grainger RM

    更新日期:1979-11-01 00:00:00

  • fumble encodes a pantothenate kinase homolog required for proper mitosis and meiosis in Drosophila melanogaster.

    abstract::A number of fundamental processes comprise the cell division cycle, including spindle formation, chromosome segregation, and cytokinesis. Our current understanding of these processes has benefited from the isolation and analysis of mutants, with the meiotic divisions in the male germline of Drosophila being particular...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Afshar K,Gönczy P,DiNardo S,Wasserman SA

    更新日期:2001-03-01 00:00:00

  • Estimating the time to the most recent common ancestor for the Y chromosome or mitochondrial DNA for a pair of individuals.

    abstract::Bayesian posterior distributions are obtained for the time to the most recent common ancestor (MRCA) for a nonrecombining segment of DNA (such as the nonpseudoautosomal arm of the Y chromosome or the mitochondrial genome) for two individuals given that they match at k out of n scored markers. We argue that the distrib...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Walsh B

    更新日期:2001-06-01 00:00:00

  • Emerging Properties and Functional Consequences of Noncoding Transcription.

    abstract::Eukaryotic genomes are rich in transcription units encoding "long noncoding RNAs" (lncRNAs). The purpose of all this transcription is unclear since most lncRNAs are quickly targeted for destruction during synthesis or shortly thereafter. As debates continue over the functional significance of many specific lncRNAs, su...

    journal_title:Genetics

    pub_type: 杂志文章,评审

    doi:10.1534/genetics.117.300095

    authors: Ard R,Allshire RC,Marquardt S

    更新日期:2017-10-01 00:00:00

  • Different Frequency in the Recovery of Crossover Products from Male and Female Gametes of Plants Hypoploid for B-a Translocations in Maize.

    abstract::The percentage of crossovers is consistently higher in plants hypoploid for six B-A translocations when crossed as males than when crossed as females; in most instances, this excess of male crossing over exceeds that found in control crosses (involving normal chromosomes). Thus, there seems to be something about the h...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Robertson DS

    更新日期:1984-05-01 00:00:00

  • Specificity of insertion by the translocatable tetracycline-resistance element Tn10.

    abstract::Genetic analysis of 131 independent transpositions of the tetracycline-resistance element Tn10 from a single site in phage P22 into the histidine operon of Salmonella typhimurium reveals that Tn10 insertions are not randomly distributed along this chromosomal target. The insertions occur in 22 different "clusters"; in...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Kleckner N,Steele DA,Reichardt K,Botstein D

    更新日期:1979-08-01 00:00:00

  • Competence for chemical reprogramming of sexual fate correlates with an intersexual molecular signature in Caenorhabditis elegans.

    abstract::In multicellular organisms, genetic programs guide cells to adopt cell fates as tissues are formed during development, maintained in adults, and repaired after injury. Here we explore how a small molecule in the environment can switch a genetic program from one fate to another. Wild-type Caenorhabditis elegans XX adul...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.114.169409

    authors: Sorokin EP,Gasch AP,Kimble J

    更新日期:2014-10-01 00:00:00

  • Epistatic Networks Jointly Influence Phenotypes Related to Metabolic Disease and Gene Expression in Diversity Outbred Mice.

    abstract::Genetic studies of multidimensional phenotypes can potentially link genetic variation, gene expression, and physiological data to create multi-scale models of complex traits. The challenge of reducing these data to specific hypotheses has become increasingly acute with the advent of genome-scale data resources. Multi-...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.116.198051

    authors: Tyler AL,Ji B,Gatti DM,Munger SC,Churchill GA,Svenson KL,Carter GW

    更新日期:2017-06-01 00:00:00

  • DDB2, DDB1A and DET1 exhibit complex interactions during Arabidopsis development.

    abstract::Damaged DNA-binding proteins 1 and 2 (DDB1 and DDB2) are subunits of the damaged DNA-binding protein complex (DDB). DDB1 is also found in the same complex as DE-ETIOLATED 1 (DET1), a negative regulator of light-mediated responses in plants. Arabidopsis has two DDB1 homologs, DDB1A and DDB1B. ddb1a single mutants have ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.107.070359

    authors: Al Khateeb WM,Schroeder DF

    更新日期:2007-05-01 00:00:00

  • The next generation of molecular markers from massively parallel sequencing of pooled DNA samples.

    abstract::Next generation sequencing (NGS) is about to revolutionize genetic analysis. Currently NGS techniques are mainly used to sequence individual genomes. Due to the high sequence coverage required, the costs for population-scale analyses are still too high to allow an extension to nonmodel organisms. Here, we show that NG...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.110.114397

    authors: Futschik A,Schlötterer C

    更新日期:2010-09-01 00:00:00

  • Identity coefficients in finite populations. I. Evolution of identity coefficients in a random mating diploid dioecious population.

    abstract::Properties of identity relation between genes are discussed, and a derivation of recurrent equations of identity coefficients in a random mating, diploid dioecious population is presented. Computations are run by repeated matrix multiplication. Results show that for effective population size (Ne) larger than 16 and no...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Chevalet C,Gillois M,Nassar RF

    更新日期:1977-07-01 00:00:00

  • A Failsafe for Sensing Chromatid Tension in Mitosis with the Histone H3 Tail in Saccharomyces cerevisiae.

    abstract::Mitotic fidelity is ensured by achieving biorientation on all paired chromosomes. The key signal for proper chromosome alignment is the tension between sister chromatids created by opposing poleward force from the spindles. In the budding yeast, the tension-sensing function requires that the Shugoshin protein, Shugosh...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.117.300606

    authors: Buehl CJ,Deng X,Luo J,Buranasudja V,Hazbun T,Kuo MH

    更新日期:2018-02-01 00:00:00

  • Power evaluations for family-based tests of association with incomplete parental genotypes.

    abstract::While a variety of methods have been developed to deal with incomplete parental genotype information in family-based association tests, sampling design issues with incomplete parental genotype data still have not received much attention. In this article, we present simulation studies with four genetic models and vario...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Yang Q,Xu X,Laird N

    更新日期:2003-05-01 00:00:00

  • Dynamics of plant mitochondrial genome: model of a three-level selection process.

    abstract::The plant mitochondrial genome is composed of a set of molecules of various sizes that generate each other through recombination between repeated sequences. Molecular observations indicate that these different molecules are present in an equilibrium state. Different compositions of molecules have been observed within ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Albert B,Godelle B,Atlan A,De Paepe R,Gouyon PH

    更新日期:1996-09-01 00:00:00

  • Gene expression intensity shapes evolutionary rates of the proteins encoded by the vertebrate genome.

    abstract::Natural selection leaves its footprints on protein-coding sequences by modulating their silent and replacement evolutionary rates. In highly expressed genes in invertebrates, these footprints are seen in the higher codon usage bias and lower synonymous divergence. In mammals, the highly expressed genes have a shorter ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.104.028944

    authors: Subramanian S,Kumar S

    更新日期:2004-09-01 00:00:00

  • Differential usage of alternative pathways of double-strand break repair in Drosophila.

    abstract::Double-strand DNA breaks can be repaired by any of several alternative mechanisms that differ greatly in the nature of the final repaired products. We used a reporter construct, designated "Repair reporter 3" (Rr3), to measure the relative usage of these pathways in Drosophila germ cells. The method works by creating ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.105.050138

    authors: Preston CR,Flores CC,Engels WR

    更新日期:2006-02-01 00:00:00

  • Repair of endonuclease-induced double-strand breaks in Saccharomyces cerevisiae: essential role for genes associated with nonhomologous end-joining.

    abstract::Repair of double-strand breaks (DSBs) in chromosomal DNA by nonhomologous end-joining (NHEJ) is not well characterized in the yeast Saccharomyces cerevisiae. Here we demonstrate that several genes associated with NHEJ perform essential functions in the repair of endonuclease-induced DSBs in vivo. Galactose-induced exp...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Lewis LK,Westmoreland JW,Resnick MA

    更新日期:1999-08-01 00:00:00