Caution on pedigree haplotype inference with software that assumes linkage equilibrium. - Wikidata - awgldk - TriplyDB

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

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

http://www.wikidata.org/entity/Q43202210

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Susceptibility genes for age-related maculopathy on chromosome 10q26.Handling marker-marker linkage disequilibrium: pedigree analysis with clustered markers CYP3A4 and CYP3A5 genotyping by Pyrosequencing Whole-genome scan, in a complex disease, using 11,245 single-nucleotide polymorphisms: comparison with microsatellites A system for exact and approximate genetic linkage analysis of SNP data in large pedigrees.Haplotype and missing data inference in nuclear families.PBAP: a pipeline for file processing and quality control of pedigree data with dense genetic markers A genome-wide linkage analysis of alcoholism on microsatellite and single-nucleotide polymorphism data, using alcohol dependence phenotypes and electroencephalogram measures Accurate haplotype inference for multiple linked single-nucleotide polymorphisms using sibship data.Ignoring intermarker linkage disequilibrium induces false-positive evidence of linkage for consanguineous pedigrees when genotype data is missing for any pedigree member.Whole-genome variance components linkage analysis using single-nucleotide polymorphisms versus microsatellites on quantitative traits of derived phenotypes from factor analysis of electroencephalogram waves.Genome scan linkage analysis comparing microsatellites and single-nucleotide polymorphisms markers for two measures of alcoholism in chromosomes 1, 4, and 7.Linkage disequilibrium across two different single-nucleotide polymorphism genome scans.PedGenie: an analysis approach for genetic association testing in extended pedigrees and genealogies of arbitrary size.Handling linkage disequilibrium in linkage analysis using dense single-nucleotide polymorphisms SNP HiTLink: a high-throughput linkage analysis system employing dense SNP data.Handling linkage disequilibrium in qualitative trait linkage analysis using dense SNPs: a two-step strategy.Genome-wide association and linkage analysis of quantitative traits: comparison of likelihood-ratio test and conditional score statistic.Detection of Mendelian consistent genotyping errors in pedigrees.Guidelines for genotyping in genomewide linkage studies: single-nucleotide-polymorphism maps versus microsatellite maps.Ignoring linkage disequilibrium among tightly linked markers induces false-positive evidence of linkage for affected sib pair analysis The value of molecular haplotypes in a family-based linkage study Genomewide scan for nonsyndromic cleft lip and palate in multigenerational Indian families reveals significant evidence of linkage at 13q33.1-34 Haplotype phasing: existing methods and new developments.Genomewide linkage scan for split-hand/foot malformation with long-bone deficiency in a large Arab family identifies two novel susceptibility loci on chromosomes 1q42.2-q43 and 6q14.1.Genetic analysis of 103 candidate genes for coronary artery disease and associated phenotypes in a founder population reveals a new association between endothelin-1 and high-density lipoprotein cholesterol Pharmacogenomic assessment of Mexican and Peruvian populations.Autosomal dominant nonsyndromic cleft lip and palate: significant evidence of linkage at 18q21.1.Pharmacogenetic pathway analysis of docetaxel elimination.A new method for haplotype inference including full-sib information.Genome-wide linkage analysis of a Parkinsonian-pyramidal syndrome pedigree by 500 K SNP arrays.GIGI: an approach to effective imputation of dense genotypes on large pedigrees Influence of solute carriers on the pharmacokinetics of CYP3A4 probes.Haplotyping methods for pedigrees.Hierarchical modeling of linkage disequilibrium: genetic structure and spatial relations CACNA1C gene polymorphisms, cardiovascular disease outcomes, and treatment response Mapping quantitative traits in unselected families: algorithms and examples.Constructing the parental linkage phase and the genetic map over distances <1 cM using pooled haploid DNA Haplotype inference in general pedigrees using the cluster variation method.Evidence for genetic linkage between a polymorphism in the adenosine 2A receptor and panic disorder.

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P2860

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

http://www.wikidata.org/entity/Q43202210

description

2002 nî lūn-bûn

@nan

2002年の論文

@ja

2002年学术文章

@wuu

2002年学术文章

@zh

2002年学术文章

@zh-cn

2002年学术文章

@zh-hans

2002年学术文章

@zh-my

2002年学术文章

@zh-sg

2002年學術文章

@yue

2002年學術文章

@zh-hant

name

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

@en

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

@nl

type

label

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

@en

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

@nl

prefLabel

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

@en

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

@nl

P1433

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P1433

American Journal of Human Genetics

P1476

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

@en

P2093

Daniel J Schaid

http://www.w3.org/2001/XMLSchema#string

Liang Wang

http://www.w3.org/2001/XMLSchema#string

Shannon K McDonnell

http://www.w3.org/2001/XMLSchema#string

Stephen N Thibodeau

http://www.w3.org/2001/XMLSchema#string

P2860

Germline mutations in the ribonuclease L gene in families showing linkage with HPC1

Parametric and nonparametric linkage analysis: a unified multipoint approach

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

Descent graphs in pedigree analysis: applications to haplotyping, location scores, and marker-sharing statistics

Linkage disequilibrium in the human genome

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

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

Analysis of the RNASEL gene in familial and sporadic prostate cancer.

An E-M algorithm and testing strategy for multiple-locus haplotypes.

Haplotyping and estimation of haplotype frequencies for closely linked biallelic multilocus genetic phenotypes including nuclear family information.

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992-995

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scholarly article

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10.1086/342666

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4

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71

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Julie M. Cunningham

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2002-10-01T00:00:00Z

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11074811

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12387273

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378555

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