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Volumn 13, Issue 1, 2012, Pages

Copy Number Variation detection from 1000 Genomes project exon capture sequencing data

Author keywords

[No Author keywords available]

Indexed keywords

BAYESIAN METHODS; COPY NUMBER VARIATIONS; EFFICIENT DETECTION; FALSE DISCOVERY RATE; GENE DELETION; GENOTYPING; HIGH IMPACT; HIGH-THROUGHPUT SEQUENCING; ILLUMINA; POWER ANALYSIS; PROJECT ANALYSIS; TARGET REGIONS;

EID: 84869021472     PISSN: None     EISSN: 14712105     Source Type: Journal    
DOI: 10.1186/1471-2105-13-305     Document Type: Article
Times cited : (23)

References (18)
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    • Gene copy number variation and common human disease
    • Fanciulli M, Petretto E, Aitman TJ. Gene copy number variation and common human disease. Clin Genet 2010, 77(3):201-213.
    • (2010) Clin Genet , vol.77 , Issue.3 , pp. 201-213
    • Fanciulli, M.1    Petretto, E.2    Aitman, T.J.3
  • 3
    • 77949362533 scopus 로고    scopus 로고
    • Upregulation of FOXM1 induces genomic instability in human epidermal keratinocytes
    • Teh MT, Gemenetzidis E, Chaplin T, Young BD, Philpott MP. Upregulation of FOXM1 induces genomic instability in human epidermal keratinocytes. Mol Cancer 2010, 9:45.
    • (2010) Mol Cancer , vol.9 , pp. 45
    • Teh, M.T.1    Gemenetzidis, E.2    Chaplin, T.3    Young, B.D.4    Philpott, M.P.5
  • 6
    • 62549145367 scopus 로고    scopus 로고
    • The role of rare structural variants in the genetics of autism spectrum disorders
    • Kusenda M, Sebat J. The role of rare structural variants in the genetics of autism spectrum disorders. Cytogenet Genome Res 2008, 123(1-4):36-43.
    • (2008) Cytogenet Genome Res , vol.123 , Issue.1-4 , pp. 36-43
    • Kusenda, M.1    Sebat, J.2
  • 12
    • 34347354302 scopus 로고    scopus 로고
    • Mutational and selective effects on copy-number variants in the human genome
    • Cooper GM, Nickerson DA, Eichler EE. Mutational and selective effects on copy-number variants in the human genome. Nat Genet 2007, 39(7 Suppl):S22-9.
    • (2007) Nat Genet , vol.39 , Issue.7 SUPPL
    • Cooper, G.M.1    Nickerson, D.A.2    Eichler, E.E.3
  • 13
    • 69749122557 scopus 로고    scopus 로고
    • Sensitive and accurate detection of copy number variants using read depth of coverage
    • Yoon S, Xuan Z, Makarov V, Ye K, Sebat J. Sensitive and accurate detection of copy number variants using read depth of coverage. Genome Res 2009, 19(9):1586-1592.
    • (2009) Genome Res , vol.19 , Issue.9 , pp. 1586-1592
    • Yoon, S.1    Xuan, Z.2    Makarov, V.3    Ye, K.4    Sebat, J.5
  • 16
    • 84975742565 scopus 로고    scopus 로고
    • A map of human genome variation from population-scale sequencing
    • 1000 Genomes Project Consortium
    • 1000 Genomes Project Consortium A map of human genome variation from population-scale sequencing. Nature 2010, 467(7319):1061-1073. 1000 Genomes Project Consortium.
    • (2010) Nature , vol.467 , Issue.7319 , pp. 1061-1073
  • 18
    • 84864609288 scopus 로고    scopus 로고
    • NHLBI Exome Sequencing Project, Quinlan AR, Nickerson DA, Eichler EE: Copy number variation detection and genotyping from exome sequence data
    • Krumm N, Sudmant PH, Ko A, O'Roak BJ, Malig M, Coe BP. NHLBI Exome Sequencing Project, Quinlan AR, Nickerson DA, Eichler EE: Copy number variation detection and genotyping from exome sequence data. Genome Res 2012, 22(8):1525-1532.
    • (2012) Genome Res , vol.22 , Issue.8 , pp. 1525-1532
    • Krumm, N.1    Sudmant, P.H.2    Ko, A.3    O'Roak, B.J.4    Malig, M.5    Coe, B.P.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.