Detection of recurrent rearrangement breakpoints from copy number data

BMC Bioinformatics

Volumn 12, Issue , 2011, Pages

  Ritz, Anna ^a   Paris, Pamela L ^b   Ittmann, Michael M ^c   Collins, Colin ^d   Raphael, Benjamin J ^a,e  

^a Brown Univerity   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c BAYLOR COLLEGE OF MEDICINE   (United States)

^d VANCOUVER PROSTATE CENTRE   (Canada)

^e BROWN UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CANCER GENOME; COPY NUMBER DATUM; GENE TRUNCATION; GLIOBLASTOMAS; NEXT-GENERATION DNA SEQUENCING; PROSTATE TUMOR; PROTEIN PHOSPHATASE; RECURRENT CNV;

DNA SEQUENCES; TUMORS;

GENES;

NON RECEPTOR PROTEIN TYROSINE PHOSPHATASE 12; PTPN12 PROTEIN, HUMAN;

ALGORITHM; ARTICLE; CHROMOSOME BREAKAGE; COMPARATIVE GENOMIC HYBRIDIZATION; COMPUTER PROGRAM; COPY NUMBER VARIATION; DNA SEQUENCE; GENE DOSAGE; GENETICS; GLIOBLASTOMA; HUMAN; MALE; NEOPLASM; PROSTATE TUMOR;

ALGORITHMS; CHROMOSOME BREAKPOINTS; COMPARATIVE GENOMIC HYBRIDIZATION; DNA COPY NUMBER VARIATIONS; GENE DOSAGE; GLIOBLASTOMA; HUMANS; MALE; NEOPLASMS; PROSTATIC NEOPLASMS; PROTEIN TYROSINE PHOSPHATASE, NON-RECEPTOR TYPE 12; SEQUENCE ANALYSIS, DNA; SOFTWARE;

EID: 79954600754     PISSN: None     EISSN: 14712105     Source Type: Journal    
DOI: 10.1186/1471-2105-12-114     Document Type: Article

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