Identification of rare germline copy number variations over-represented in five human cancer types

Molecular Cancer

Volumn 14, Issue 1, 2015, Pages

  Park, Richard W ^a,b   Kim, Tae Min ^b,c   Kasif, Simon ^a,d,e   Park, Peter J ^b,e  

^a BOSTON UNIVERSITY   (United States)

^b Harvard Medical School Center for Biomedical Informatics   (United States)

^c The Catholic University of Korea   (South Korea)

^d Boston University   (United States)

^e HARVARD MIT DIVISION OF HEALTH SCIENCES AND TECHNOLOGY   (United States)

Author keywords

Array CGH; Cancer susceptibility; CNV association study; DNA copy number

Indexed keywords

DNA; MICRORNA; RNA;

ARTICLE; BRAIN CANCER; BREAST CANCER; CANCER RISK; CANCER SUSCEPTIBILITY; CASE CONTROL STUDY; CONTROLLED STUDY; COPY NUMBER VARIATION; GENE DOSAGE; GENETIC ASSOCIATION; GERMLINE COPY NUMBER VARIATION; HUMAN; HUMAN GENOME; KIDNEY CANCER; KIDNEY CARCINOMA; MAJOR CLINICAL STUDY; OVARY CANCER; SINGLE NUCLEOTIDE POLYMORPHISM; FEMALE; GENETIC PREDISPOSITION; GENETICS; GENOME-WIDE ASSOCIATION STUDY; GENOTYPE; MALE; NEOPLASM; PROCEDURES; RISK;

CASE-CONTROL STUDIES; DNA COPY NUMBER VARIATIONS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENOME-WIDE ASSOCIATION STUDY; GENOTYPE; HUMANS; MALE; NEOPLASMS; POLYMORPHISM, SINGLE NUCLEOTIDE; RISK;

EID: 84925856279     PISSN: None     EISSN: 14764598     Source Type: Journal    
DOI: 10.1186/s12943-015-0292-6     Document Type: Article

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