Detection and integration of genotyping errors in statistical genetics
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Homozygous nonsense mutations in KIAA1279 are associated with malformations of the central and enteric nervous systems.Wide disparity in genetic admixture among Mexican Americans from San Antonio, TXEpilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutationsNeuropathy target esterase gene mutations cause motor neuron diseaseMutations in TMEM76* cause mucopolysaccharidosis IIIC (Sanfilippo C syndrome)Contributions of PTCH gene variants to isolated cleft lip and palateComparative linkage analysis and visualization of high-density oligonucleotide SNP array dataEffects of DNA mass on multiple displacement whole genome amplification and genotyping performance.Replication of linkage on chromosome 7q22 and association of the regional Reelin gene with working memory in schizophrenia familiesGenomewide linkage screen for Waldenstrom macroglobulinemia susceptibility loci in high-risk familiesComparison of microsatellites versus single-nucleotide polymorphisms in a genome linkage screen for prostate cancer-susceptibility LociHeritability and preliminary genome-wide linkage analysis of arsenic metabolites in urineAssociation of Cardiometabolic Genes with Arsenic Metabolism Biomarkers in American Indian Communities: The Strong Heart Family Study (SHFS)Truncation of the E3 ubiquitin ligase component FBXO31 causes non-syndromic autosomal recessive intellectual disability in a Pakistani familyA transmission disequilibrium test for general pedigrees that is robust to the presence of random genotyping errors and any number of untyped parents.ALDH2 is associated to alcohol dependence and is the major genetic determinant of "daily maximum drinks" in a GWAS study of an isolated rural Chinese sampleGenome-wide linkage scan for loci of musical aptitude in Finnish families: evidence for a major locus at 4q22.Increasing genotype-phenotype model determinism: application to bivariate reading/language traits and epistatic interactions in language-impaired families.A genomewide search finds major susceptibility loci for gallbladder disease on chromosome 1 in Mexican Americans.Statistical genetic analysis of serological measures of common, chronic infections in Alaska Native participants in the GOCADAN study.Probability of detection of genotyping errors and mutations as inheritance inconsistencies in nuclear-family dataValue of Mendelian laws of segregation in families: data quality control, imputation, and beyondQuantitative analysis of low-density SNP data for parentage assignment and estimation of family contributions to pooled samples.Data for Genetic Analysis Workshop 18: human whole genome sequence, blood pressure, and simulated phenotypes in extended pedigrees.Joint analysis of sequence data and single-nucleotide polymorphism data using pedigree information for imputation and recombination inference.Using Mendelian inheritance errors as quality control criteria in whole genome sequencing data set.Simultaneous estimation of QTL effects and positions when using genotype data with errors.Mega2: data-handling for facilitating genetic linkage and association analyses.PEDSTATS: descriptive statistics, graphics and quality assessment for gene mapping data.Precision and type I error rate in the presence of genotype errors and missing parental data: a comparison between the original transmission disequilibrium test (TDT) and TDTae statisticsThe impact of data quality on the identification of complex disease genes: experience from the Family Blood Pressure Program.Maximum-likelihood estimation of allelic dropout and false allele error rates from microsatellite genotypes in the absence of reference data.Estimating genealogies from linked marker data: a Bayesian approach.Imputing missing genotypic data of single-nucleotide polymorphisms using neural networks.Estimating ethnic admixture from pedigree data.Elucidation of the 'Honeycrisp' pedigree through haplotype analysis with a multi-family integrated SNP linkage map and a large apple (Malus×domestica) pedigree-connected SNP data setDetection of genotyping errors by Hardy-Weinberg equilibrium testing.An examination of the genotyping error detection function of SIMWALK2.Pedigree and genotype errors in the Framingham Heart StudyEffect of genotyping error in model-free linkage analysis using microsatellite or single-nucleotide polymorphism marker maps.
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Detection and integration of genotyping errors in statistical genetics
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 08 January 2002
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Detection and integration of genotyping errors in statistical genetics
@en
Detection and integration of genotyping errors in statistical genetics.
@nl
type
label
Detection and integration of genotyping errors in statistical genetics
@en
Detection and integration of genotyping errors in statistical genetics.
@nl
prefLabel
Detection and integration of genotyping errors in statistical genetics
@en
Detection and integration of genotyping errors in statistical genetics.
@nl
P2860
P356
P1476
Detection and integration of genotyping errors in statistical genetics
@en
P2093
Jeanette C Papp
Kenneth Lange
P2860
P304
P356
10.1086/338920
P407
P577
2002-01-08T00:00:00Z