Copy number variation accuracy in genome-wide association studies

Human Heredity

Volumn 71, Issue 3, 2011, Pages 141-147

  Lin, Peng ^a   Hartz, Sarah M ^a   Wang, Jen Chyong ^a   Krueger, Robert F ^b   Foroud, Tatiana M ^c   Edenberg, Howard J ^c   Nurnberger Jr , John I ^c   Brooks, Andrew I ^d   Tischfield, Jay A ^d   Almasy, Laura ^e   Webb, Bradley T ^f   Hesselbrock, Victor M ^g   Porjesz, Bernice ^h   Goate, Alison M ^a   Bierut, Laura J ^a   Rice, John P ^a  

^a WASHINGTON UNIVERSITY   (United States)

^b UNIVERSITY OF MINNESOTA   (United States)

^c INDIANA UNIVERSITY   (United States)

^d RUTGERS UNIVERSITY   (United States)

^e SOUTHWEST FOUNDATION FOR BIOMEDICAL RESEARCH   (United States)

^f VIRGINIA COMMONWEALTH UNIVERSITY   (United States)

^g UNIVERSITY OF CONNECTICUT HEALTH CENTER   (United States)

^h SUNY DOWNSTATE MEDICAL CENTER   (United States)

Author keywords

Accuracy; Copy number variations; False positives; Genome wide association studies

Indexed keywords

ARTICLE; CLINICAL RESEARCH; COPY NUMBER VARIATION; FOLLOW UP; GENETIC ASSOCIATION; LABORATORY DIAGNOSIS; MICROARRAY ANALYSIS; PREDICTIVE VALUE; REPRODUCIBILITY; SENSITIVITY ANALYSIS;

DNA COPY NUMBER VARIATIONS; GENOME-WIDE ASSOCIATION STUDY; HUMANS; POLYMORPHISM, SINGLE NUCLEOTIDE; PREDICTIVE VALUE OF TESTS; REPRODUCIBILITY OF RESULTS; SOFTWARE;

EID: 79960751640     PISSN: 00015652     EISSN: 14230062     Source Type: Journal    
DOI: 10.1159/000324683     Document Type: Article

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