Identification and analysis of error types in high-throughput genotyping
about
Genomewide linkage study in 1,176 affected sister pair families identifies a significant susceptibility locus for endometriosis on chromosome 10q26.Likelihood-based estimation of microsatellite mutation ratesGenetic dissection of the human leukocyte antigen region by use of haplotypes of Tasmanians with multiple sclerosisGenotyping errors in a calibrated DNA register: implications for identification of individualsGenomewide linkage scan of schizophrenia in a large multicenter pedigree sample using single nucleotide polymorphismsMycobacterium tuberculosis complex genetic diversity: mining the fourth international spoligotyping database (SpolDB4) for classification, population genetics and epidemiology"Are we there yet?": Deciding when one has demonstrated specific genetic causation in complex diseases and quantitative traits.Trend-TDT - a transmission/disequilibrium based association test on functional mini/microsatellites.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 dataThe 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.Detection of genotyping errors by Hardy-Weinberg equilibrium testing.Influence of genotyping error in linkage mapping for complex traits--an analytic study.Evaluation of microsatellite variation in the 1000 Genomes Project pilot studies is indicative of the quality and utility of the raw data and alignments.Current trends in microsatellite genotyping.Undetected genotyping errors cause apparent overtransmission of common alleles in the transmission/disequilibrium testGenomewide linkage scan for schizophrenia susceptibility loci among Ashkenazi Jewish families shows evidence of linkage on chromosome 10q22.Genomewide linkage scan for bipolar-disorder susceptibility loci among Ashkenazi Jewish familiesA genome wide linkage scan for dizygotic twinning in 525 families of mothers of dizygotic twins.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 1qGenomewide high-density SNP linkage analysis of 236 Japanese families supports the existence of schizophrenia susceptibility loci on chromosomes 1p, 14q, and 20p.Confidence-based somatic mutation evaluation and prioritizationMicrosatellite standardization and evaluation of genotyping error in a large multi-partner research programme for conservation of Atlantic salmon (Salmo salar L.).A tale of two genotypes: consistency between two high-throughput genotyping centers.Identification of mildew resistance in wild and cultivated Central Asian grape germplasmBioinformatics challenges for personalized medicineHLA and genomewide allele sharing in dizygotic twins.lobSTR: A short tandem repeat profiler for personal genomes.A comprehensive literature review of haplotyping software and methods for use with unrelated individuals.Factors affecting statistical power in the detection of genetic association.Queensland Centre for Mental Health Research: the first 17 years.Rules for resolving Mendelian inconsistencies in nuclear pedigrees typed for two-allele markers.Genotyping errors: causes, consequences and solutions.Functional genetic polymorphisms and female reproductive disorders: part II--endometriosisRelationship inference from trios of individuals, in the presence of typing error.A genomewide search for type 2 diabetes-susceptibility genes in indigenous Australians.Detection and integration of genotyping errors in statistical geneticsLinkage of Paget disease of bone to a novel region on human chromosome 18q23.Presence of large deletions in kindreds with autism.
P2860
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P2860
Identification and analysis of error types in high-throughput genotyping
description
2000 nî lūn-bûn
@nan
2000 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի օգոստոսին 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
Identification and analysis of error types in high-throughput genotyping
@ast
Identification and analysis of error types in high-throughput genotyping
@en
Identification and analysis of error types in high-throughput genotyping
@nl
type
label
Identification and analysis of error types in high-throughput genotyping
@ast
Identification and analysis of error types in high-throughput genotyping
@en
Identification and analysis of error types in high-throughput genotyping
@nl
prefLabel
Identification and analysis of error types in high-throughput genotyping
@ast
Identification and analysis of error types in high-throughput genotyping
@en
Identification and analysis of error types in high-throughput genotyping
@nl
P2093
P2860
P356
P1476
Identification and analysis of error types in high-throughput genotyping
@en
P2093
D F Levinson
J W Barlow
S A Treloar
P2860
P304
P356
10.1086/303048
P407
P577
2000-08-02T00:00:00Z