WaveCNV: Allele-specific copy number alterations in primary tumors and xenograft models from next-generation sequencing

Bioinformatics

Volumn 30, Issue 6, 2014, Pages 768-774

  Holt, Carson ^a   Losic, Bojan ^a   Pai, Deepa ^a   Zhao, Zhen ^a   Trinh, Quang ^a   Syam, Sujata ^a   Arshadi, Niloofar ^a   Jang, Gun Ho ^a   Ali, Johar ^a   Beck, Tim ^a   McPherson, John ^a   Muthuswamy, Lakshmi B ^a,b  

^a ONTARIO INSTITUTE FOR CANCER RESEARCH   (Canada)

^b UNIVERSITY OF TORONTO   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ALGORITHM; ALLELE; ANEUPLOIDY; ANIMAL; ARTICLE; COMPUTER PROGRAM; COPY NUMBER VARIATION; DNA SEQUENCE; DRUG SCREENING; GENETICS; HIGH THROUGHPUT SEQUENCING; HUMAN; METHODOLOGY; MOUSE; NEOPLASM;

ALGORITHMS; ALLELES; ANEUPLOIDY; ANIMALS; DNA COPY NUMBER VARIATIONS; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; MICE; NEOPLASMS; SEQUENCE ANALYSIS, DNA; SOFTWARE; XENOGRAFT MODEL ANTITUMOR ASSAYS;

EID: 84897853363     PISSN: 13674803     EISSN: 14602059     Source Type: Journal    
DOI: 10.1093/bioinformatics/btt611     Document Type: Article

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