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Bioinformatics
Volumn 32, Issue 15, 2016, Pages 2375-2377
Canvas: Versatile and scalable detection of copy number variants
Author keywords

[No Author keywords available]
Indexed keywords

ALGORITHM; COPY NUMBER VARIATION; EXOME; HUMAN; NEOPLASM; SOFTWARE;
EID: 84991498358     PISSN: 13674803     EISSN: 14602059     Source Type: Journal    
DOI: 10.1093/bioinformatics/btw163     Document Type: Article
Times cited : (140)
References (10)
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    • Amarasinghe, K.C.1
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    • Control-FREEC: A tool for assessing copy number and allelic content using next generation sequencing data
    • Boeva, V. et al. (2011) Control-FREEC: a tool for assessing copy number and allelic content using next generation sequencing data. Bioinformatics, 28, 423-425.
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    • Boeva, V.1
  • 5
    • 84924336542 scopus 로고    scopus 로고
    • TITAN: Inference of copy number architectures in clonal cell populations from tumor whole-genome sequence data
    • Ha, G. et al. (2014) TITAN: inference of copy number architectures in clonal cell populations from tumor whole-genome sequence data. Genome Res., 24, 1881-1893.
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    • Ha, G.1
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    • EXCAVATOR: Detecting copy number variants from whole-exome sequencing data
    • Magi, A. et al. (2013) EXCAVATOR: detecting copy number variants from whole-exome sequencing data. Genome Biol., 14, R120.
    • (2013) Genome Biol. , vol.14 , pp. R120
    • Magi, A.1
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    • Evaluation of somatic copy number estimation tools for whole-exome sequencing data
    • Nam, J. et al. (2015) Evaluation of somatic copy number estimation tools for whole-exome sequencing data. Brief. Bioinf., 17, 185-192.
    • (2015) Brief. Bioinf. , vol.17 , pp. 185-192
    • Nam, J.1
  • 8
    • 77953870937 scopus 로고    scopus 로고
    • Tracing the tumor lineage
    • Navin, N.E. (2010) Tracing the tumor lineage. Mol. Oncol., 4, 267-283.
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    • Navin, N.E.1
  • 9
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    • Newman, S. (2013) The relative timing of mutations in a breast cancer genome. PLoS One, 8, e64991.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.