Simple and efficient analysis of disease association with missing genotype data
about
A flexible and accurate genotype imputation method for the next generation of genome-wide association studiesA unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individualsSimpute: an efficient solution for dense genotypic data.Missing data imputation and haplotype phase inference for genome-wide association studies.Practical issues in imputation-based association mapping.Iterative two-pass algorithm for missing data imputation in SNP arrays.A general framework for studying genetic effects and gene-environment interactions with missing data.Analyses and comparison of imputation-based association methodsKinase insert domain receptor/vascular endothelial growth factor receptor 2 (KDR) genetic variation is associated with ovarian hyperstimulation syndromeMethods for investigating gene-environment interactions in candidate pathway and genome-wide association studies.A flexible model for association analysis in sibships with missing genotype data.A new genotype imputation method with tolerance to high missing rate and rare variantsAnalysis of Case-Control Association Studies: SNPs, Imputation and Haplotypes.Practical considerations for imputation of untyped markers in admixed populations.Family-based association tests using genotype data with uncertainty.Imputation without doing imputation: a new method for the detection of non-genotyped causal variants.SeqEM: an adaptive genotype-calling approach for next-generation sequencing studiesA fine-mapping study of 7 top scoring genes from a GWAS for major depressive disorder.Association studies with imputed variants using expectation-maximization likelihood-ratio tests.Analysis of untyped SNPs: maximum likelihood and imputation methods.ETHNOPRED: a novel machine learning method for accurate continental and sub-continental ancestry identification and population stratification correctionBayesian epistasis association mapping via SNP imputation.Re-ranking sequencing variants in the post-GWAS era for accurate causal variant identificationJackknife-based gene-gene interactiontests for untyped SNPsProper Use of Allele-Specific Expression Improves Statistical Power for cis-eQTL Mapping with RNA-Seq DataAssociation of SOCS1 (- 820) (rs33977706) gene polymorphism with chronic periodontitis: A case-control study in BraziliansThe Molecular Revolution in Cutaneous Biology: The Era of Genome-Wide Association Studies and Statistical, Big Data, and Computational Topics.Optimal methods for using posterior probabilities in association testing.Genotype-imputation accuracy across worldwide human populations.Estimating the posterior probability that genome-wide association findings are true or false.Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo.Cytokine genetic polymorphisms and prostate cancer aggressivenessAssociation of restless legs syndrome variants in Korean patients with restless legs syndrome.ATRIUM: testing untyped SNPs in case-control association studies with related individuals.An efficient study design to test parent-of-origin effects in family trios.Bayesian quantitative trait locus mapping using inferred haplotypes.Interaction association analysis of imputed SNPs in case-control and follow-up studies.An NOS3 Haplotype is Protective against Hypertension in a Caucasian Population.Fast and robust association tests for untyped SNPs in case-control studies.Comparison of six statistics of genetic association regarding their ability to discriminate between causal variants and genetically linked markers.
P2860
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P2860
Simple and efficient analysis of disease association with missing genotype data
description
2008 nî lūn-bûn
@nan
2008 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Simple and efficient analysis of disease association with missing genotype data
@ast
Simple and efficient analysis of disease association with missing genotype data
@en
Simple and efficient analysis of disease association with missing genotype data.
@nl
type
label
Simple and efficient analysis of disease association with missing genotype data
@ast
Simple and efficient analysis of disease association with missing genotype data
@en
Simple and efficient analysis of disease association with missing genotype data.
@nl
prefLabel
Simple and efficient analysis of disease association with missing genotype data
@ast
Simple and efficient analysis of disease association with missing genotype data
@en
Simple and efficient analysis of disease association with missing genotype data.
@nl
P2093
P2860
P1476
Simple and efficient analysis of disease association with missing genotype data
@en
P2093
P2860
P304
P356
10.1016/J.AJHG.2007.11.004
P407
P577
2008-02-01T00:00:00Z