Genome-wide analysis of the role of copy-number variation in pancreatic cancer risk

Frontiers in Genetics

Volumn 5, Issue FEB, 2014, Pages

  Willis, Jason A ^a   Mukherjee, Semanti ^a   Orlow, Irene ^a   Viale, Agnes ^a   Offit, Kenneth ^a   Kurtz, Robert C ^a   Olson, Sara H ^a   Klein, Robert J ^a  

^a MEMORIAL SLOAN KETTERING CANCER CENTER   (United States)

Author keywords

Cancer risk; CNVs; Copy number variation; Pancreatic cancer; SNP microarrays

Indexed keywords

ADULT; AGED; ARTICLE; CANCER RISK; CONTROLLED STUDY; COPY NUMBER VARIATION; FEMALE; GENE CLUSTER; GENE LOCUS; GENETIC ASSOCIATION; GENETIC DIFFERENCE; GENETIC PREDISPOSITION; GENETIC RISK; GENETIC VARIABILITY; GENOME ANALYSIS; GENOTYPING TECHNIQUE; HUMAN; MAJOR CLINICAL STUDY; MALE; MICROARRAY ANALYSIS; MIDDLE AGED; MULTIVARIATE LOGISTIC REGRESSION ANALYSIS; OVERLAPPING GENE; PANCREAS CANCER; POPULATION GENETIC STRUCTURE; QUALITY CONTROL; SINGLE NUCLEOTIDE POLYMORPHISM; SPECTROPHOTOMETRY;

EID: 84897744896     PISSN: None     EISSN: 16648021     Source Type: Journal    
DOI: 10.3389/fgene.2014.00029     Document Type: Article

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