A multipoint method for detecting genotyping errors and mutations in sibling-pair linkage data.
about
Admixture dynamics in Hispanics: a shift in the nuclear genetic ancestry of a South American population isolateEvidence for an apartheid-like social structure in early Anglo-Saxon EnglandComparative linkage analysis and visualization of high-density oligonucleotide SNP array dataComparison of microsatellites versus single-nucleotide polymorphisms in a genome linkage screen for prostate cancer-susceptibility LociMutation screening and association analysis of six candidate genes for autism on chromosome 7qCandidate-gene screening and association analysis at the autism-susceptibility locus on chromosome 16p: evidence of association at GRIN2A and ABATSASI-Seq: sample assurance Spike-Ins, and highly differentiating 384 barcoding for Illumina sequencing.A transmission/disequilibrium test that allows for genotyping errors in the analysis of single-nucleotide polymorphism data.Probability of detection of genotyping errors and mutations as inheritance inconsistencies in nuclear-family dataSimultaneous estimation of QTL effects and positions when using genotype data with errors.Sibship reconstruction from genetic data with typing errors.A genome-wide linkage analysis of alcoholism on microsatellite and single-nucleotide polymorphism data, using alcohol dependence phenotypes and electroencephalogram measuresThe impact of data quality on the identification of complex disease genes: experience from the Family Blood Pressure Program.Detection of genotyping errors by Hardy-Weinberg equilibrium testing.An examination of the genotyping error detection function of SIMWALK2.Using overall allele-sharing to detect the presence of large-scale data errors and parameter misspecification in sib-pair linkage studies.Effect of genotyping error in model-free linkage analysis using microsatellite or single-nucleotide polymorphism marker maps.Influence of genotyping error in linkage mapping for complex traits--an analytic study.Deviations from hardy-weinberg equilibrium in parental and unaffected sibling genotype dataMissing call bias in high-throughput genotyping.Detection of Mendelian consistent genotyping errors in pedigrees.Undetected genotyping errors cause apparent overtransmission of common alleles in the transmission/disequilibrium testLinkage analysis of extremely discordant and concordant sibling pairs identifies quantitative-trait loci that influence variation in the human personality trait neuroticismGuidelines for genotyping in genomewide linkage studies: single-nucleotide-polymorphism maps versus microsatellite maps.Genomewide significant linkage to recurrent, early-onset major depressive disorder on chromosome 15q.Incorporating genotyping uncertainty in haplotype inference for single-nucleotide polymorphisms.A genomewide scan for loci predisposing to type 2 diabetes in a U.K. population (the Diabetes UK Warren 2 Repository): analysis of 573 pedigrees provides independent replication of a susceptibility locus on chromosome 1qA genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p.Whole-genome screening in ankylosing spondylitis: evidence of non-MHC genetic-susceptibility loci.Identification and analysis of error types in high-throughput genotypingImproved inference of relationship for pairs of individualsReplication strategies for rare variant complex trait association studies via next-generation sequencing.Genome scan for loci predisposing to anxiety disorders using a novel multivariate approach: strong evidence for a chromosome 4 risk locus.Genotyping error detection through tightly linked markers.A tale of two genotypes: consistency between two high-throughput genotyping centers.Integration of SNP genotyping confidence scores in IBD inferenceEvidence for linkage and association with reading disability on 6p21.3-22.Factors affecting statistical power in the detection of genetic association.Rules for resolving Mendelian inconsistencies in nuclear pedigrees typed for two-allele markers.Genotyping errors: causes, consequences and solutions.
P2860
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P2860
A multipoint method for detecting genotyping errors and mutations in sibling-pair linkage data.
description
2000 nî lūn-bûn
@nan
2000 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի մարտին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
A multipoint method for detect ...... in sibling-pair linkage data.
@ast
A multipoint method for detect ...... in sibling-pair linkage data.
@en
type
label
A multipoint method for detect ...... in sibling-pair linkage data.
@ast
A multipoint method for detect ...... in sibling-pair linkage data.
@en
prefLabel
A multipoint method for detect ...... in sibling-pair linkage data.
@ast
A multipoint method for detect ...... in sibling-pair linkage data.
@en
P2860
P356
P1476
A multipoint method for detect ...... in sibling-pair linkage data.
@en
P2093
P2860
P304
P356
10.1086/302861
P407
P577
2000-03-28T00:00:00Z