Genome-wide algorithm for detecting CNV associations with diseases

BMC Bioinformatics

Volumn 12, Issue , 2011, Pages

  Xu, Yaji ^a,b,c   Peng, Bo ^a   Fu, Yunxin ^b   Amos, Christopher I ^a  

^a UNIVERSITY OF TEXAS MD ANDERSON CANCER CENTER   (United States)

^b UNIVERSITY OF TEXAS SCHOOL OF PUBLIC HEALTH   (United States)

^c YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALTERNATIVE PROCEDURES; DISEASE ASSOCIATIONS; FALSE POSITIVE RATES; INTENSITY VALUES; LOGISTIC REGRESSION MODELING; SIMULATION STUDIES; SINGLE NUCLEOTIDE POLYMORPHISMS; STATISTICAL ALGORITHM;

COMPUTER SIMULATION; GENES; HIDDEN MARKOV MODELS; REGRESSION ANALYSIS; RISK PERCEPTION; SIGNAL DETECTION;

ALGORITHMS;

ALGORITHM; ARTICLE; COMPUTER PROGRAM; COMPUTER SIMULATION; COPY NUMBER VARIATION; DISEASES; GENETIC ASSOCIATION; GENETICS; HUMAN; HUMAN GENOME; MELANOMA; REGRESSION ANALYSIS; SENSITIVITY AND SPECIFICITY; SINGLE NUCLEOTIDE POLYMORPHISM; STATISTICAL MODEL;

ALGORITHMS; COMPUTER SIMULATION; DISEASE; DNA COPY NUMBER VARIATIONS; GENOME, HUMAN; GENOME-WIDE ASSOCIATION STUDY; HUMANS; MELANOMA; MODELS, STATISTICAL; POLYMORPHISM, SINGLE NUCLEOTIDE; REGRESSION ANALYSIS; SENSITIVITY AND SPECIFICITY; SOFTWARE;

EID: 79961140556     PISSN: None     EISSN: 14712105     Source Type: Journal    
DOI: 10.1186/1471-2105-12-331     Document Type: Article

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