Exome sequencing-based copy-number variation and loss of heterozygosity detection: ExomeCNV

Bioinformatics

Volumn 27, Issue 19, 2011, Pages 2648-2654

  Sathirapongsasuti, Jarupon Fah ^a,b,c   Lee, Hane ^c   Horst, Basil A J ^c,d   Brunner, Georg ^e   Cochran, Alistair J ^c   Binder, Scott ^c   Quackenbush, John ^a,b   Nelson, Stanley F ^c  

^a HARVARD SCHOOL OF PUBLIC HEALTH   (United States)

^b DANA FARBER CANCER INSTITUTE   (United States)

^c UNIVERSITY OF CALIFORNIA   (United States)

^d NewYork Presbyterian Hospital   (United States)

^e Department of Cancer Research   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ALGORITHM; ARTICLE; BIOLOGICAL MODEL; COPY NUMBER VARIATION; DNA SEQUENCE; EXOME; GENETICS; GENOTYPE; HETEROZYGOSITY LOSS; HUMAN; MELANOMA; METHODOLOGY; NUCLEOTIDE SEQUENCE; SINGLE NUCLEOTIDE POLYMORPHISM; SKIN TUMOR;

ALGORITHMS; BASE SEQUENCE; DNA COPY NUMBER VARIATIONS; EXOME; GENOTYPE; HUMANS; LOSS OF HETEROZYGOSITY; MELANOMA; MODELS, GENETIC; POLYMORPHISM, SINGLE NUCLEOTIDE; SEQUENCE ANALYSIS, DNA; SKIN NEOPLASMS;

EID: 80053446554     PISSN: 13674803     EISSN: 14602059     Source Type: Journal    
DOI: 10.1093/bioinformatics/btr462     Document Type: Article

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