A customized and versatile high-density genotyping array for the mouse. - Wikidata - wikimedia - TriplyDB

A customized and versatile high-density genotyping array for the mouse.

A customized and versatile high-density genotyping array for the mouse.

http://www.wikidata.org/entity/Q37327534

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Genomic mapping of social behavior traits in a F2 cross derived from mice selectively bred for high aggression.Genetic implication of a novel thiamine transporter in human hypertension.Evaluating genetic markers and neurobiochemical analytes for fluoxetine response using a panel of mouse inbred strains Connecting Anxiety and Genomic Copy Number Variation: A Genome-Wide Analysis in CD-1 Mice Genetic Architecture of Atherosclerosis in Mice: A Systems Genetics Analysis of Common Inbred Strains The Genetic Architecture of Hearing Impairment in Mice: Evidence for Frequency-Specific Genetic Determinants A cellular genetics approach identifies gene-drug interactions and pinpoints drug toxicity pathway nodes A performance study of the impact of recombination on species tree analysis Mapping the genomic architecture of adaptive traits with interspecific introgressive origin: a coalescent-based approach Collaborative Cross and Diversity Outbred data resources in the Mouse Phenome Database Molecular and phenotypic distinction of the very recently evolved insular subspecies Mus musculus helgolandicus ZIMMERMANN, 1953 A multi-megabase copy number gain causes maternal transmission ratio distortion on mouse chromosome 2 Deconstructing Mus gemischus: advances in understanding ancestry, structure, and variation in the genome of the laboratory mouse SNP microarray analyses reveal copy number alterations and progressive genome reorganization during tumor development in SVT/t driven mice breast cancer Integration of mouse and human genome-wide association data identifies KCNIP4 as an asthma gene Preservation Analysis of Macrophage Gene Coexpression Between Human and Mouse Identifies PARK2 as a Genetically Controlled Master Regulator of Oxidative Phosphorylation in Humans.Integration of genome-wide association and extant brain expression QTL identifies candidate genes influencing prepulse inhibition in inbred F1 mice.Identification of quantitative trait loci influencing skeletal architecture in mice: emergence of Cdh11 as a primary candidate gene regulating femoral morphology Serious limitations of the QTL/microarray approach for QTL gene discovery.Antipsychotic-induced vacuous chewing movements and extrapyramidal side effects are highly heritable in mice.Multiple imputation of missing phenotype data for QTL mapping.Staggered chromosomal hybrid zones in the house mouse: relevance to reticulate evolution and speciation.Accessing Data Resources in the Mouse Phenome Database for Genetic Analysis of Murine Life Span and Health Span A forest-based feature screening approach for large-scale genome data with complex structures.Integrating human and rodent data to identify the genetic factors involved in chronic kidney disease High-resolution sex-specific linkage maps of the mouse reveal polarized distribution of crossovers in male germline Mapping allele-specific DNA methylation: a new tool for maximizing information from GWAS.Commercially available outbred mice for genome-wide association studies.Integrated genomics of susceptibility to alkylator-induced leukemia in mice An HMM-based comparative genomic framework for detecting introgression in eukaryotes.Selective breeding and selection mapping using a novel wild-derived heterogeneous stock of mice revealed two closely-linked loci for tameness.Genomes of the Mouse Collaborative Cross.Selected rapporteur summaries from the XX World Congress of Psychiatric Genetics, Hamburg, Germany, October 14-18, 2012.Regulation of sex determination in mice by a non-coding genomic region.Measures of linkage disequilibrium among neighbouring SNPs indicate asymmetries across the house mouse hybrid zone.Parent-independent genotyping for constructing an ultrahigh-density linkage map based on population sequencing.Fine mapping in 94 inbred mouse strains using a high-density haplotype resource.Identification of a QTL in Mus musculus for alcohol preference, withdrawal, and Ap3m2 expression using integrative functional genomics and precision genetics.Fine-mapping QTLs in advanced intercross lines and other outbred populations.CGDSNPdb: a database resource for error-checked and imputed mouse SNPs.

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P2860

A customized and versatile high-density genotyping array for the mouse.

http://www.wikidata.org/entity/Q37327534

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on 09 August 2009

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

A customized and versatile high-density genotyping array for the mouse.

@en

A customized and versatile high-density genotyping array for the mouse.

@nl

type

label

A customized and versatile high-density genotyping array for the mouse.

@en

A customized and versatile high-density genotyping array for the mouse.

@nl

prefLabel

A customized and versatile high-density genotyping array for the mouse.

@en

A customized and versatile high-density genotyping array for the mouse.

@nl

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A customized and versatile high-density genotyping array for the mouse

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P2093

Beverly J Paigen

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

Fernando Pardo-Manuel de Villena

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

Gary A Churchill

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Hyuna Yang

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Jin Szatkiewicz

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Lucie N Hutchins

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Timothy A Bell

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Yueming Ding

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P2860

A common and unstable copy number variant is associated with differences in Glo1 expression and anxiety-like behavior

Ultraconserved Elements in the Human Genome

Silhouette scores for assessment of SNP genotype clusters

A high-resolution map of segmental DNA copy number variation in the mouse genome

Gene expression and isoform variation analysis using Affymetrix Exon Arrays.

Ascertainment bias in studies of human genome-wide polymorphism.

Mouse segmental duplication and copy number variation

An imputed genotype resource for the laboratory mouse

The Collaborative Cross at Oak Ridge National Laboratory: developing a powerful resource for systems genetics

Widespread monoallelic expression on human autosomes.

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10.1038/NMETH.1359

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9

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6

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2009-08-09T00:00:00Z

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26729802

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19668205

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