A transmission/disequilibrium test that allows for genotyping errors in the analysis of single-nucleotide polymorphism data.
about
A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?A transmission disequilibrium test for general pedigrees that is robust to the presence of random genotyping errors and any number of untyped parents.Trend-TDT - a transmission/disequilibrium based association test on functional mini/microsatellites.Impact of genotyping errors on the type I error rate and the power of haplotype-based association methods.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.A family-based likelihood ratio test for general pedigree structures that allows for genotyping error and missing data.Detection of genotyping errors by Hardy-Weinberg equilibrium testing.SUP: an extension to SLINK to allow a larger number of marker loci to be simulated in pedigrees conditional on trait values.The merits of testing Hardy-Weinberg equilibrium in the analysis of unmatched case-control data: a cautionary note.Approaches to handling incomplete data in family-based association testing.Using the longest significance run to estimate region-specific p-values in genetic association mapping studies.Estimating the single nucleotide polymorphism genotype misclassification from routine double measurements in a large epidemiologic sample.Deviations from hardy-weinberg equilibrium in parental and unaffected sibling genotype dataOn quality control measures in genome-wide association studies: a test to assess the genotyping quality of individual probands in family-based association studies and an application to the HapMap data.In vitro vs in silico detected SNPs for the development of a genotyping array: what can we learn from a non-model species?Optimal two-stage design for case-control association analysis incorporating genotyping errors.Detection of Mendelian consistent genotyping errors in pedigrees.ALG: automated genotype calling of Luminex assaysUndetected genotyping errors cause apparent overtransmission of common alleles in the transmission/disequilibrium testA 3.9-centimorgan-resolution human single-nucleotide polymorphism linkage map and screening set.A quality control algorithm for filtering SNPs in genome-wide association studies.Recent developments in genomewide association scans: a workshop summary and reviewGenome-wide association filtering using a highly locus-specific transmission/disequilibrium testDifferentiating population stratification from genotyping error using family data.Family-based association tests using genotype data with uncertainty.Parent-child DRD4 genotype as a potential biomarker for oppositional, anxiety, and repetitive behaviors in children with autism spectrum disorderTDT-HET: a new transmission disequilibrium test that incorporates locus heterogeneity into the analysis of family-based association data.Examination of potential overlap in autism and language loci on chromosomes 2, 7, and 13 in two independent samples ascertained for specific language impairmentSNP genotyping on a genome-wide amplified DOP-PCR templateAssessing genuine parents-offspring trios for genetic association studies.Genotyping error detection through tightly linked markers.Genome-wide association studies of adolescent idiopathic scoliosis suggest candidate susceptibility genes.Integrated model of de novo and inherited genetic variants yields greater power to identify risk genes.A tale of two genotypes: consistency between two high-throughput genotyping centers.A powerful nonparametric statistical framework for family-based association analyses.CHD7 gene polymorphisms are associated with susceptibility to idiopathic scoliosis.A genomewide linkage scan for quantitative-trait loci for obesity phenotypes.African-derived genetic polymorphisms in TNFAIP3 mediate risk for autoimmunityEvaluating the evidence for transmission distortion in human pedigrees.
P2860
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P2860
A transmission/disequilibrium test that allows for genotyping errors in the analysis of single-nucleotide polymorphism data.
description
2001 nî lūn-bûn
@nan
2001 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
A transmission/disequilibrium ...... -nucleotide polymorphism data.
@ast
A transmission/disequilibrium ...... -nucleotide polymorphism data.
@en
type
label
A transmission/disequilibrium ...... -nucleotide polymorphism data.
@ast
A transmission/disequilibrium ...... -nucleotide polymorphism data.
@en
prefLabel
A transmission/disequilibrium ...... -nucleotide polymorphism data.
@ast
A transmission/disequilibrium ...... -nucleotide polymorphism data.
@en
P2093
P2860
P356
P1476
A transmission/disequilibrium ...... -nucleotide polymorphism data.
@en
P2093
P2860
P304
P356
10.1086/321981
P407
P577
2001-07-05T00:00:00Z