Identification and analysis of error types in high-throughput genotyping - Wikidata - awgldk - TriplyDB

Identification and analysis of error types in high-throughput genotyping

Identification and analysis of error types in high-throughput genotyping

http://www.wikidata.org/entity/Q34142683

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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 rates Genetic dissection of the human leukocyte antigen region by use of haplotypes of Tasmanians with multiple sclerosis Genotyping errors in a calibrated DNA register: implications for identification of individuals Genomewide linkage scan of schizophrenia in a large multicenter pedigree sample using single nucleotide polymorphisms Mycobacterium 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 data The 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 test Genomewide 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 families A 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 1q Genomewide 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 prioritization Microsatellite 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 germplasm Bioinformatics challenges for personalized medicine HLA 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--endometriosis Relationship 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 genetics Linkage of Paget disease of bone to a novel region on human chromosome 18q23.Presence of large deletions in kindreds with autism.

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P2860

Identification and analysis of error types in high-throughput genotyping

http://www.wikidata.org/entity/Q34142683

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

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2000年論文

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2000年論文

@zh-hant

2000年論文

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2000年論文

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2000年論文

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2000年论文

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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

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P1433

American Journal of Human Genetics

P1476

Identification and analysis of error types in high-throughput genotyping

@en

P2093

B Mowry

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

D F Levinson

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

J W Barlow

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K R Ewen

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M Bahlo

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

S A Treloar

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S J Foote

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P2860

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

Genetic and physical mapping of the Treacher Collins syndrome locus: refinement of the localization to chromosome 5q32-33.2

Hypervariabflity of simple sequences as a general source for polymorphic DNA markers

High resolution of human evolutionary trees with polymorphic microsatellites

A multipoint method for detecting genotyping errors and mutations in sibling-pair linkage data.

Systematic detection of errors in genetic linkage data.

Microsatellite mapping of the gene causing weaver disease in cattle will allow the study of an associated quantitative trait locus.

Genetic variation of microsatellite loci in a bottlenecked species: the northern hairy-nosed wombat Lasiorhinus krefftii.

Detection of highly polymorphic microsatellite loci in a species with little allozyme polymorphism.

Using quality measures to facilitate allele calling in high-throughput genotyping.

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727-736

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10.1086/303048

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3

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67

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12396801

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10924406

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1287531

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