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Volumn 13, Issue 7, 2013, Pages 647-650

Integrating next-generation sequencing into clinical cancer diagnostics

Author keywords

[No Author keywords available]

Indexed keywords

CANCER DIAGNOSIS; CANCER GENETICS; DNA SEQUENCE; GENE TECHNOLOGY; HUMAN; NEOPLASM; REVIEW; EDITORIAL; GENETICS; HIGH THROUGHPUT SEQUENCING; HUMAN GENOME; MOLECULAR DIAGNOSIS; NUCLEOTIDE SEQUENCE; NEOPLASMS;

EID: 84898689509     PISSN: 14737159     EISSN: 17448352     Source Type: Journal    
DOI: 10.1586/14737159.2013.820551     Document Type: Review
Times cited : (5)

References (14)
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    • Jiang Q, Turner T, Sosa MX, Rakha A, Arnold S, Chakravarti A. Rapid and efficient human mutation detection using a bench-top next-generation DNA sequencer. Hum Mutat. 2012; 33(1):281-9.
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    • Jiang, Q.1    Turner, T.2    Sosa, M.X.3    Rakha, A.4    Arnold, S.5    Chakravarti, A.6
  • 4
    • 84867400465 scopus 로고    scopus 로고
    • Development of a next-generation sequencing method for BRCA mutation screening: A comparison between a high-throughput and a benchtop platform
    • Chan M, Ji SM, Yeo ZX, Gan L, Yap E, Yap YS, et al. Development of a next-generation sequencing method for BRCA mutation screening: a comparison between a high-throughput and a benchtop platform. J. Mol. Diagn. 2012; 14(6):602-12.
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    • Chan, M.1    Ji, S.M.2    Yeo, Z.X.3    Gan, L.4    Yap, E.5    Yap, Y.S.6
  • 5
    • 84875519657 scopus 로고    scopus 로고
    • Nonoptical massive parallel DNA sequencing of BRCA1 and BRCA2 genes in a diagnostic setting
    • Costa JL, Sousa S, Justino A, Kay T, Fernandes S, Cirnes L, et al. Nonoptical massive parallel DNA sequencing of BRCA1 and BRCA2 genes in a diagnostic setting. Hum Mutat. 2013; 34(4):629-35.
    • (2013) Hum Mutat. , vol.34 , Issue.4 , pp. 629-635
    • Costa, J.L.1    Sousa, S.2    Justino, A.3    Kay, T.4    Fernandes, S.5    Cirnes, L.6
  • 7
    • 79955483667 scopus 로고    scopus 로고
    • A framework for variation discovery and genotyping using next-generation DNA sequencing data
    • DePristo MA, Banks E, Poplin R, Garimella KV, Maguire JR, Hartl C et al. A framework for variation discovery and genotyping using next-generation DNA sequencing data. Nat. Genet. 2011; 43(5):491-8.
    • (2011) Nat. Genet. , vol.43 , Issue.5 , pp. 491-498
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  • 8
    • 84866564536 scopus 로고    scopus 로고
    • Improving indel detection specificity of the Ion Torrent PGM benchtop sequencer
    • Yeo ZX, Chan M, Yap YS, Ang P, Rozen S, Lee AS. Improving indel detection specificity of the Ion Torrent PGM benchtop sequencer. PLoS One 2012; 7(9):e45798.
    • (2012) PLoS One , vol.7 , Issue.9
    • Yeo, Z.X.1    Chan, M.2    Yap, Y.S.3    Ang, P.4    Rozen, S.5    Lee, A.S.6
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    • 84857691276 scopus 로고    scopus 로고
    • Rapid and efficient human mutation detection using a bench-top next-generation DNA sequencer
    • doi: 10.1002/humu.21602. (Epub ahead of print
    • Jiang Q, Turner T, Sosa M, Rakha A, Arnold S, Chakravarti A. Rapid and efficient human mutation detection using a bench-top next-generation DNA sequencer. Hum. Mutat. 2011; doi: 10.1002/humu.21602. (Epub ahead of print).
    • (2011) Hum. Mutat.
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    • Next-generation sequencing for cancer diagnostics: A practical perspective
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.