Inference on haplotype effects in case-control studies using unphased genotype data. - Wikidata - awgldk - TriplyDB

Inference on haplotype effects in case-control studies using unphased genotype data.

Inference on haplotype effects in case-control studies using unphased genotype data.

http://www.wikidata.org/entity/Q33195240

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Meta-analysis of haplotype-association studies: comparison of methods and empirical evaluation of the literature The BTNL2 gene and sarcoidosis susceptibility in African Americans and Whites Association of FKBP5 polymorphisms and childhood abuse with risk of posttraumatic stress disorder symptoms in adults Genetic studies of a cluster of acute lymphoblastic leukemia cases in Churchill County, Nevada Evaluation of logistic Bayesian LASSO for identifying association with rare haplotypes The ApoAI-CIII-AIV gene cluster and its relation to lipid levels in type 2 diabetes mellitus and coronary heart disease: determination of a novel susceptible haplotype Gene, region and pathway level analyses in whole-genome studies Robust estimation for homoscedastic regression in the secondary analysis of case-control data.Multilevel cross-dependent binary longitudinal data.A Note on Penalized Regression Spline Estimation in the Secondary Analysis of Case-Control Data.Multinomial logistic regression approach to haplotype association analysis in population-based case-control studies.A haplotype-based test of association using data from cohort and nested case-control epidemiologic studies.Fine mapping functional sites or regions from case-control data using haplotypes of multiple linked SNPs.Haplotype effects on human survival: logistic regression models applied to unphased genotype data.Test of association between haplotypes and phenotypes in case-control studies: examination of validity of the application of an algorithm for samples from cohort or clinical trials to case-control samples using simulated and real data.Conditional likelihood methods for haplotype-based association analysis using matched case-control data.Likelihood-based association analysis for nuclear families and unrelated subjects with missing genotype data.Estimating haplotype effects on dichotomous outcome for unphased genotype data using a weighted penalized log-likelihood approach.FCRL3 promoter 169 CC homozygosity is associated with susceptibility to rheumatoid arthritis in Dutch Caucasians A new JAVA interface implementation of THESIAS: testing haplotype effects in association studies.Retrospective analysis of main and interaction effects in genetic association studies of human complex traits Estimating effects of rare haplotypes on failure time using a penalized Cox proportional hazards regression model.Haplotype reconstruction error as a classical misclassification problem: introducing sensitivity and specificity as error measures.Association tests based on the principal-component analysis SNPAnalyzer 2.0: a web-based integrated workbench for linkage disequilibrium analysis and association analysis.Detecting purely epistatic multi-locus interactions by an omnibus permutation test on ensembles of two-locus analyses.Estimating haplotype effects for survival data.PCA-based bootstrap confidence interval tests for gene-disease association involving multiple SNPs A general framework for studying genetic effects and gene-environment interactions with missing data.An omnibus permutation test on ensembles of two-locus analyses can detect pure epistasis and genetic heterogeneity in genome-wide association studies.Modeling Informatively Missing Genotypes in Haplotype Analysis.A flexible model for association analysis in sibships with missing genotype data.Analysis of Case-Control Association Studies: SNPs, Imputation and Haplotypes.Haplotype kernel association test as a powerful method to identify chromosomal regions harboring uncommon causal variants.Practical considerations for imputation of untyped markers in admixed populations.Polymorphisms in CRHR1 and the serotonin transporter loci: gene x gene x environment interactions on depressive symptoms Reducing bias of allele frequency estimates by modeling SNP genotype data with informative missingness Two genes encoding immune-regulatory molecules (LAG3 and IL7R) confer susceptibility to multiple sclerosis.Regression-based association analysis with clustered haplotypes through use of genotypes.Evaluating statistical significance in two-stage genomewide association studies.

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Inference on haplotype effects in case-control studies using unphased genotype data.

http://www.wikidata.org/entity/Q33195240

description

2003 nî lūn-bûn

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2003 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

2003 թվականի նոյեմբերին հրատարակված գիտական հոդված

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2003年の論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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2003年论文

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name

Inference on haplotype effects in case-control studies using unphased genotype data.

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Inference on haplotype effects in case-control studies using unphased genotype data.

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type

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Inference on haplotype effects in case-control studies using unphased genotype data.

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Inference on haplotype effects in case-control studies using unphased genotype data.

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prefLabel

Inference on haplotype effects in case-control studies using unphased genotype data.

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Inference on haplotype effects in case-control studies using unphased genotype data.

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Inference on haplotype effects in case-control studies using unphased genotype data.

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Michael P Epstein

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P2860

Searching for genetic determinants in the new millennium

A candidate prostate cancer susceptibility gene at chromosome 17p

A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms

The future of genetic studies of complex human diseases

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

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

Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease

Accuracy of haplotype frequency estimation for biallelic loci, via the expectation-maximization algorithm for unphased diploid genotype data.

Genetic analysis of case/control data using estimated haplotype frequencies: application to APOE locus variation and Alzheimer's disease.

Choosing haplotype-tagging SNPS based on unphased genotype data using a preliminary sample of unrelated subjects with an example from the Multiethnic Cohort Study.

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1316-1329

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10.1086/380204

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