Detecting multiple causal rare variants in exome sequence data

Genetic Epidemiology

Volumn 35, Issue SUPPL. 1, 2011, Pages

  Ye, Kenny Q ^a   Engelman, Corinne D ^b  

^a ALBERT EINSTEIN COLLEGE OF MEDICINE   (United States)

^b UNIVERSITY OF WISCONSIN SCHOOL OF MEDICINE AND PUBLIC HEALTH   (United States)

Author keywords

Bayesian; Pathways; Simulated

Indexed keywords

ALLELE; ARTICLE; BAYES THEOREM; CAUSAL ATTRIBUTION; EFFECT SIZE; EXOME; GENE; GENE FREQUENCY; GENE SEQUENCE; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOTYPE; HUMAN; HUMAN GENOME; PHENOTYPE; SIGNAL TRANSDUCTION; SINGLE NUCLEOTIDE POLYMORPHISM; WORKSHOP;

CAUSALITY; EXOME; GENETIC PREDISPOSITION TO DISEASE; HUMAN GENOME PROJECT; HUMANS; MODELS, GENETIC; MOLECULAR EPIDEMIOLOGY; POLYMORPHISM, SINGLE NUCLEOTIDE; SEQUENCE ANALYSIS;

EID: 82455172172     PISSN: 07410395     EISSN: 10982272     Source Type: Journal    
DOI: 10.1002/gepi.20644     Document Type: Article

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