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Volumn 32, Issue 6, 2016, Pages 926-928

Global copy number profiling of cancer genomes

(8) Wang, Xuefeng a,b Chen, Mengjie c Yu, Xiaoqing d Pornputtapong, Natapol b,e Chen, Hao f Zhang, Nancy R g Powers, R Scott h Krauthammer, Michael b,e

a STONY BROOK UNIVERSITY (United States)

b YALE UNIVERSITY SCHOOL OF MEDICINE (United States)

c University of North Carolina at Chapel Hill (United States)

d Department of Biostatistics ^* (United States)

e YALE UNIVERSITY (United States)

f UNIVERSITY OF CALIFORNIA (United States)

g UNIVERSITY OF PENNSYLVANIA (United States)

h STONY BROOK UNIVERSITY (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALGORITHM; COPY NUMBER VARIATION; DNA SEQUENCE; GENE FREQUENCY; HUMAN; HUMAN GENOME; NEOPLASM;

ALGORITHMS; DNA COPY NUMBER VARIATIONS; GENE FREQUENCY; GENOME, HUMAN; HUMANS; NEOPLASMS; SEQUENCE ANALYSIS, DNA;

EID: 84962195786 PISSN: 13674803 EISSN: 14602059 Source Type: Journal
DOI: 10.1093/bioinformatics/btv676 Document Type: Article

Times cited : (3)

References (8)

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2
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- Favero, F.¹

5
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- Allele-specific amplification in cancer revealed by SNP array analysis
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- A general framework for analyzing tumor subclonality uing SNP array and DNA sequencing data
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- Allele-specific copy number analysis of tumors
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.