Joint analyses of disease and correlated quantitative phenotypes using next-generation sequencing data

Genetic Epidemiology

Volumn 35, Issue SUPPL. 1, 2011, Pages

  Melton, Phillip E ^a   Pankratz, Nathan ^b  

^a SOUTHWEST FOUNDATION FOR BIOMEDICAL RESEARCH   (United States)

^b UNIVERSITY OF MINNESOTA MEDICAL SCHOOL   (United States)

Author keywords

Combined phenotype analysis; Dimensionality reduction; Next generation sequencing; Quantitative traits; Rare variants

Indexed keywords

ARTICLE; EXOME; FAMILY STUDY; GENE LINKAGE DISEQUILIBRIUM; GENE SEQUENCE; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC LINKAGE; GENETIC VARIABILITY; GOLD STANDARD; HUMAN; MEDICAL RESEARCH; PHENOTYPE; PLEIOTROPY; QUANTITATIVE ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM;

CASE-CONTROL STUDIES; EXOME; GENETIC PREDISPOSITION TO DISEASE; HUMAN GENOME PROJECT; HUMANS; MODELS, GENETIC; MOLECULAR EPIDEMIOLOGY; PHENOTYPE; PRINCIPAL COMPONENT ANALYSIS; REGRESSION ANALYSIS; SEQUENCE ANALYSIS;

EID: 82455219119     PISSN: 07410395     EISSN: 10982272     Source Type: Journal    
DOI: 10.1002/gepi.20653     Document Type: Article

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