A 3.9-centimorgan-resolution human single-nucleotide polymorphism linkage map and screening set. - Wikidata - awgldk - TriplyDB

A 3.9-centimorgan-resolution human single-nucleotide polymorphism linkage map and screening set.

A 3.9-centimorgan-resolution human single-nucleotide polymorphism linkage map and screening set.

http://www.wikidata.org/entity/Q33905163

about

Human subtelomeric WASH genes encode a new subclass of the WASP family A population-genetic test of founder effects and implications for Ashkenazi Jewish diseases.Handling marker-marker linkage disequilibrium: pedigree analysis with clustered markers Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia: suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sample.Integrating linkage and radiation hybrid mapping data for bovine chromosome 15 Whole-genome scan, in a complex disease, using 11,245 single-nucleotide polymorphisms: comparison with microsatellites Genomewide linkage searches for Mendelian disease loci can be efficiently conducted using high-density SNP genotyping arrays Genetic analysis of genome-wide variation in human gene expression Linkage studies of catechol-O-methyltransferase (COMT) and dopamine-beta-hydroxylase (DBH) cDNA expression levels.Reconstituting the frequency spectrum of ascertained single-nucleotide polymorphism data.Data for Genetic Analysis Workshop (GAW) 15, Problem 1: genetics of gene expression variation in humans Linkage and association analyses of microsatellites and single-nucleotide polymorphisms in nuclear families Comparison of microsatellites, single-nucleotide polymorphisms (SNPs) and composite markers derived from SNPs in linkage analysis Evaluation of linkage disequilibrium and its effect on non-parametric multipoint linkage analysis using two high density single-nucleotide polymorphism mapping panels.Automated SNP detection from a large collection of white spruce expressed sequences: contributing factors and approaches for the categorization of SNPs Elevated rates of sister chromatid exchange at chromosome ends.In vitro whole-genome analysis identifies a susceptibility locus for HIV-1.Artificial neural networks for linkage analysis of quantitative gene expression phenotypes and evaluation of gene x gene interactions.Joint linkage and imprinting analyses of GAW15 rheumatoid arthritis and gene expression data SNP HiTLink: a high-throughput linkage analysis system employing dense SNP data.Meiotic recombination in human oocytes.Regional differences in recombination hotspots between two chicken populations Linkage disequilibrium and inference of ancestral recombination in 538 single-nucleotide polymorphism clusters across the human genome Sequence-based linkage analysis Guidelines for genotyping in genomewide linkage studies: single-nucleotide-polymorphism maps versus microsatellite maps.A combined linkage-physical map of the human genome Ethnicity and human genetic linkage maps.Maternal age and chromosomally abnormal pregnancies: what we know and what we wish we knew.Analysis of human meiotic recombination events with a parent-sibling tracing approach Cytological studies of recombination in rhesus males.Sex, not genotype, determines recombination levels in mice.Extensive natural variation for cellular hydrogen peroxide release is genetically controlled.In silico method for inferring genotypes in pedigrees.Sex: differences in mutation, recombination, selection, gene flow, and genetic drift.Diverse mutational mechanisms cause pathogenic subtelomeric rearrangements.Multipoint linkage analysis with many multiallelic or dense diallelic markers: Markov chain-Monte Carlo provides practical approaches for genome scans on general pedigrees.The future of genetic testing for drug response.Whole genomewide linkage screen for neural tube defects reveals regions of interest on chromosomes 7 and 10.Widespread RNA and DNA sequence differences in the human transcriptome.Polymorphic variation in human meiotic recombination.

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P2860

A 3.9-centimorgan-resolution human single-nucleotide polymorphism linkage map and screening set.

http://www.wikidata.org/entity/Q33905163

description

2003 nî lūn-bûn

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2003 թուականի Յուլիսին հրատարակուած գիտական յօդուած

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2003 թվականի հուլիսին հրատարակված գիտական հոդված

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2003年の論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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2003年论文

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A 3.9-centimorgan-resolution h ...... linkage map and screening set.

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A 3.9-centimorgan-resolution h ...... linkage map and screening set.

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A 3.9-centimorgan-resolution h ...... linkage map and screening set.

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American Journal of Human Genetics

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A 3.9-centimorgan-resolution h ...... linkage map and screening set.

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Alexander F Wilson

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Andrew G Clark

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Arkadiy Silbergleit

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Arthur L Holden

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Buena Chui

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Carl T Yamashiro

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Chunsheng He

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Claudia de Toma

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Emily S Winn-Deen

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Eric Lai

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Initial sequencing and analysis of the human genome

The Sequence of the Human Genome

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

Mutation analysis of the spastin gene (SPG4) in patients with hereditary spastic paraparesis

Strategies for multilocus linkage analysis in humans

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms

Construction of a genetic linkage map in man using restriction fragment length polymorphisms

A fast and scalable radiation hybrid map construction and integration strategy

The future of genetic studies of complex human diseases

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271-284

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10.1086/377137

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2

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Margaret A. Pericak-Vance

Ellen M. Wijsman

Kyriacos Markianos

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2003-07-03T00:00:00Z

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10676138

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12844283

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single-nucleotide polymorphism

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1180367

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