Next generation genome-wide association tool: design and coverage of a high-throughput European-optimized SNP array
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Characterizing Race/Ethnicity and Genetic Ancestry for 100,000 Subjects in the Genetic Epidemiology Research on Adult Health and Aging (GERA) CohortClinical review: Genome-wide association studies of skeletal phenotypes: what we have learned and where we are headedStrategies for Imputing and Analyzing Rare Variants in Association StudiesImputation of the rare HOXB13 G84E mutation and cancer risk in a large population-based cohortLimitations of the human reference genome for personalized genomicsGenome-wide association study identifies TNFSF15 and POU2AF1 as susceptibility loci for primary biliary cirrhosis in the Japanese populationBig Data Analytics for Genomic MedicineGenome-wide association study of subclinical interstitial lung disease in MESA.A Large Genome-Wide Association Study of Age-Related Hearing Impairment Using Electronic Health RecordsWhat if we had whole-genome sequence data for millions of individuals?Cell-autonomous correction of ring chromosomes in human induced pluripotent stem cellsQuantifying the mapping precision of genome-wide association studies using whole-genome sequencing dataApplications of the 1000 Genomes Project resourcesTissue Sources for Accurate Measurement of Germline DNA Genotypes in Prostate Cancer Patients Treated With Radical Prostatectomy.Simple, standardized incorporation of genetic risk into non-genetic risk prediction tools for complex traits: coronary heart disease as an example.Functional logistic regression approach to detecting gene by longitudinal environmental exposure interaction in a case-control study.Nocturnal asthma and the importance of race/ethnicity and genetic ancestryThe impact of improved microarray coverage and larger sample sizes on future genome-wide association studiesA genome-wide survey of transgenerational genetic effects in autism.Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study dataAssessment of the geographic origins of pinewood nematode isolates via single nucleotide polymorphism in effector genesDevelopment of the catfish 250K SNP array for genome-wide association studies.Enrichment of Minor Alleles of Common SNPs and Improved Risk Prediction for Parkinson's Disease.ClinLabGeneticist: a tool for clinical management of genetic variants from whole exome sequencing in clinical genetic laboratories.Genome-wide association study identifies ABCG2 (BCRP) as an allopurinol transporter and a determinant of drug response.Differences in the Genetic Susceptibility to Age-Related Macular Degeneration Clinical SubtypesIntegrating 400 million variants from 80,000 human samples with extensive annotations: towards a knowledge base to analyze disease cohorts.A large multiethnic genome-wide association study of prostate cancer identifies novel risk variants and substantial ethnic differences.Smokescreen: a targeted genotyping array for addiction researchAn integrated analysis tool for analyzing hybridization intensities and genotypes using new-generation population-optimized human arrays.Multiethnic genome-wide association study identifies ethnic-specific associations with body mass index in Hispanics and African AmericansA Powerful Procedure for Pathway-Based Meta-analysis Using Summary Statistics Identifies 43 Pathways Associated with Type II Diabetes in European Populations.Genotyping Informatics and Quality Control for 100,000 Subjects in the Genetic Epidemiology Research on Adult Health and Aging (GERA) CohortConcept and design of a genome-wide association genotyping array tailored for transplantation-specific studiesPleiotropic Mechanisms Indicated for Sex Differences in AutismReverse Pathway Genetic Approach Identifies Epistasis in Autism Spectrum Disorders.Japonica array: improved genotype imputation by designing a population-specific SNP array with 1070 Japanese individualsGenome-wide association screens for Achilles tendon and ACL tears and tendinopathy.Contrasting genetic architectures of schizophrenia and other complex diseases using fast variance-components analysisA Multidisciplinary Phenotyping and Genotyping Analysis of a Mapping Population Enables Quality to Be Combined with Yield in Rice.
P2860
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P2860
Next generation genome-wide association tool: design and coverage of a high-throughput European-optimized SNP array
description
2011 nî lūn-bûn
@nan
2011 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Next generation genome-wide as ...... t European-optimized SNP array
@ast
Next generation genome-wide as ...... t European-optimized SNP array
@en
type
label
Next generation genome-wide as ...... t European-optimized SNP array
@ast
Next generation genome-wide as ...... t European-optimized SNP array
@en
prefLabel
Next generation genome-wide as ...... t European-optimized SNP array
@ast
Next generation genome-wide as ...... t European-optimized SNP array
@en
P2093
P2860
P1433
P1476
Next generation genome-wide as ...... t European-optimized SNP array
@en
P2093
Alan Williams
Andrea Finn
Carlos Iribarren
Catherine Schaefer
Charles Quesenberry
Christine Aquino
Christopher C Wen
Dana Ludwig
David Smethurst
P2860
P356
10.1016/J.YGENO.2011.04.005
P50
P577
2011-04-30T00:00:00Z