Localising loci underlying complex trait variation using Regional Genomic Relationship Mapping. - Wikidata - wikimedia - TriplyDB

Localising loci underlying complex trait variation using Regional Genomic Relationship Mapping.

Localising loci underlying complex trait variation using Regional Genomic Relationship Mapping.

http://www.wikidata.org/entity/Q34450357

about

Genome-wide association reveals QTL for growth, bone and in vivo carcass traits as assessed by computed tomography in Scottish Blackface lambs.Quantitative trait loci mapping for canine hip dysplasia and its related traits in UK Labrador Retrievers A new tool called DISSECT for analysing large genomic data sets using a Big Data approach.Analysis of the genetics of boar taint reveals both single SNPs and regional effects Fine-mapping host genetic variation underlying outcomes to Mycobacterium bovis infection in dairy cows.Local exome sequences facilitate imputation of less common variants and increase power of genome wide association studies.Complex variation in measures of general intelligence and cognitive change.Heterogeneity of genetic architecture of body size traits in a free-living population.Regional Heritability Mapping to identify loci underlying genetic variation of complex traits The Genetic Architecture of Arsenic Metabolism Efficiency:A SNP-Based Heritability Study of Bangladeshi Adults.Genomic regions underlying susceptibility to bovine tuberculosis in Holstein-Friesian cattle Antagonistic genetic correlations for milking traits within the genome of dairy cattle Genome-wide association and regional heritability mapping to identify loci underlying variation in nematode resistance and body weight in Scottish Blackface lambs.Conserved Genetic Architecture Underlying Individual Recombination Rate Variation in a Wild Population of Soay Sheep (Ovis aries)The power of regional heritability analysis for rare and common variant detection: simulations and application to eye biometrical traits.The heritability and patterns of DNA methylation in normal human colorectum A Combined Pathway and Regional Heritability Analysis Indicates NETRIN1 Pathway Is Associated With Major Depressive Disorder.Genome-wide association study identifies novel loci associated with resistance to bovine tuberculosis.Regional heritability mapping method helps explain missing heritability of blood lipid traits in isolated populations.Immunogenomics of gastrointestinal nematode infection in ruminants - breeding for resistance to produce food sustainably and safely.Genome-wide Regional Heritability Mapping Identifies a Locus Within the TOX2 Gene Associated With Major Depressive Disorder.The Nature of Genetic Variation for Complex Traits Revealed by GWAS and Regional Heritability Mapping Analyses.Variation in Recombination Rate and Its Genetic Determinism in Sheep Populations.A joint analysis to identify loci underlying variation in nematode resistance in three European sheep populations.Genome-Wide Association and Genomic Selection for Resistance to Amoebic Gill Disease in Atlantic Salmon.Haplotype Heritability Mapping Method Uncovers Missing Heritability of Complex Traits.Functional Validation of Candidate Genes Detected by Genomic Feature Models.Regional heritability mapping and genome-wide association identify loci for complex growth, wood and disease resistance traits in Eucalyptus.Detecting polygenic selection in marine populations by combining population genomics and quantitative genetics approaches.Alleles versus mutations: Understanding the evolution of genetic architecture requires a molecular perspective on allelic origins.GWAS by GBLUP: Single and Multimarker EMMAX and Bayes Factors, with an Example in Detection of a Major Gene for Horse Gait.A Genomic Region Containing REC8 and RNF212B Is Associated with Individual Recombination Rate Variation in a Wild Population of Red Deer (Cervus elaphus).

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Localising loci underlying complex trait variation using Regional Genomic Relationship Mapping.

http://www.wikidata.org/entity/Q34450357

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2012 nî lūn-bûn

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2012 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

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2012 թվականի հոտեմբերին հրատարակված գիտական հոդված

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P2860

Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations

Genetic architecture of complex traits and accuracy of genomic prediction: coat colour, milk-fat percentage, and type in Holstein cattle as contrasting model traits

Finding the missing heritability of complex diseases

Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease

Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters

Hundreds of variants clustered in genomic loci and biological pathways affect human height

PLINK: a tool set for whole-genome association and population-based linkage analyses

SLC2A9 is a newly identified urate transporter influencing serum urate concentration, urate excretion and gout

The mystery of missing heritability: Genetic interactions create phantom heritability

The future of genetic studies of complex human diseases

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