Literature DB >> 11791212

Score tests for association between traits and haplotypes when linkage phase is ambiguous.

Daniel J Schaid1, Charles M Rowland, David E Tines, Robert M Jacobson, Gregory A Poland.   

Abstract

A key step toward the discovery of a gene related to a trait is the finding of an association between the trait and one or more haplotypes. Haplotype analyses can also provide critical information regarding the function of a gene; however, when unrelated subjects are sampled, haplotypes are often ambiguous because of unknown linkage phase of the measured sites along a chromosome. A popular method of accounting for this ambiguity in case-control studies uses a likelihood that depends on haplotype frequencies, so that the haplotype frequencies can be compared between the cases and controls; however, this traditional method is limited to a binary trait (case vs. control), and it does not provide a method of testing the statistical significance of specific haplotypes. To address these limitations, we developed new methods of testing the statistical association between haplotypes and a wide variety of traits, including binary, ordinal, and quantitative traits. Our methods allow adjustment for nongenetic covariates, which may be critical when analyzing genetically complex traits. Furthermore, our methods provide several different global tests for association, as well as haplotype-specific tests, which give a meaningful advantage in attempts to understand the roles of many different haplotypes. The statistics can be computed rapidly, making it feasible to evaluate the associations between many haplotypes and a trait. To illustrate the use of our new methods, they are applied to a study of the association of haplotypes (composed of genes from the human-leukocyte-antigen complex) with humoral immune response to measles vaccination. Limited simulations are also presented to demonstrate the validity of our methods, as well as to provide guidelines on how our methods could be used.

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Year:  2001        PMID: 11791212      PMCID: PMC384917          DOI: 10.1086/338688

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  37 in total

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Authors:  S W Guo
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4.  Fine-scale genetic mapping based on linkage disequilibrium: theory and applications.

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5.  Molecular haplotyping of genetic markers 10 kb apart by allele-specific long-range PCR.

Authors:  S Michalatos-Beloin; S A Tishkoff; K L Bentley; K K Kidd; G Ruano
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6.  HAPLO: a program using the EM algorithm to estimate the frequencies of multi-site haplotypes.

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7.  Maximum-likelihood estimation of molecular haplotype frequencies in a diploid population.

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8.  Likelihood methods for locating disease genes in nonequilibrium populations.

Authors:  N L Kaplan; W G Hill; B S Weir
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9.  A powerful likelihood method for the analysis of linkage disequilibrium between trait loci and one or more polymorphic marker loci.

Authors:  J D Terwilliger
Journal:  Am J Hum Genet       Date:  1995-03       Impact factor: 11.025

10.  Testing for linkage disequilibrium in genotypic data using the Expectation-Maximization algorithm.

Authors:  M Slatkin; L Excoffier
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  730 in total

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2.  Caution on pedigree haplotype inference with software that assumes linkage equilibrium.

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3.  Association of PDE4B polymorphisms and schizophrenia in Northwestern Han Chinese.

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5.  Asymptotic tests of association with multiple SNPs in linkage disequilibrium.

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6.  Polymorphisms in innate immunity genes and lung cancer risk in Xuanwei, China.

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7.  Sequence variations of the human MPDZ gene and association with alcoholism in subjects with European ancestry.

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8.  Analysis of 30 genes (355 SNPS) related to energy homeostasis for association with adiposity in European-American and Yup'ik Eskimo populations.

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9.  Effect of macrophage migration inhibitory factor (MIF) gene variants and MIF serum concentrations on the risk of type 2 diabetes: results from the MONICA/KORA Augsburg Case-Cohort Study, 1984-2002.

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10.  Association between urokinase haplotypes and outcome from infection-associated acute lung injury.

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