메뉴 건너뛰기




Volumn 115, Issue 3-4, 2006, Pages 205-214

Development of bioinformatics resources for display and analysis of copy number and other structural variants in the human genome

Author keywords

[No Author keywords available]

Indexed keywords

GENOMIC DNA;

EID: 33751527925     PISSN: 14248581     EISSN: None     Source Type: Journal    
DOI: 10.1159/000095916     Document Type: Article
Times cited : (173)

References (26)
  • 1
    • 4444375366 scopus 로고    scopus 로고
    • As normal as normal can be?
    • Carter NP: As normal as normal can be? Nat Genet 36:931-932 (2004).
    • (2004) Nat Genet , vol.36 , pp. 931-932
    • Carter, N.P.1
  • 2
    • 27144485366 scopus 로고    scopus 로고
    • Human genome: Patchwork people
    • Check E: Human genome: patchwork people. Nature 437:1084-1086 (2005).
    • (2005) Nature , vol.437 , pp. 1084-1086
    • Check, E.1
  • 3
    • 0037837485 scopus 로고    scopus 로고
    • Genome-wide detection of segmental duplications and potential assembly errors in the human genome sequence
    • Cheung J, Estivill X, Khaja R, MacDonald JR, Lau K, et al: Genome-wide detection of segmental duplications and potential assembly errors in the human genome sequence. Genome Biol 4:R25 (2003).
    • (2003) Genome Biol , vol.4
    • Cheung, J.1    Estivill, X.2    Khaja, R.3    MacDonald, J.R.4    Lau, K.5
  • 4
    • 0036107052 scopus 로고    scopus 로고
    • Time for a unified system of mutation description and reporting: A review of locus-specific mutation databases
    • Claustres M, Horaitis O, Vanevski M, Cotton RG: Time for a unified system of mutation description and reporting: a review of locus-specific mutation databases. Genome Res 12:680-688 (2002).
    • (2002) Genome Res , vol.12 , pp. 680-688
    • Claustres, M.1    Horaitis, O.2    Vanevski, M.3    Cotton, R.G.4
  • 6
    • 29444438167 scopus 로고    scopus 로고
    • Widening the spectrum of human genetic variation
    • Eichler EE: Widening the spectrum of human genetic variation. Nat Genet 38:9-11 (2006).
    • (2006) Nat Genet , vol.38 , pp. 9-11
    • Eichler, E.E.1
  • 7
  • 8
    • 33746363353 scopus 로고    scopus 로고
    • Structural variants: Changing the landscape of chromosomes and design of disease studies
    • Feuk L, Marshall CR, Wintle RF, Scherer SW: Structural variants: changing the landscape of chromosomes and design of disease studies. Hum Mol Genet 15 Spec No 1:R57-66 (2006b).
    • (2006) Hum Mol Genet , vol.15 , Issue.SPEC NO 1
    • Feuk, L.1    Marshall, C.R.2    Wintle, R.F.3    Scherer, S.W.4
  • 11
    • 13444259868 scopus 로고    scopus 로고
    • The Molecular Biology Database Collection: 2005 Update
    • Galperin MY: The Molecular Biology Database Collection: 2005 update. Nucleic Acids Res 33:D5-24 (2005).
    • (2005) Nucleic Acids Res , vol.33
    • Galperin, M.Y.1
  • 12
    • 20044377204 scopus 로고    scopus 로고
    • The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility
    • Gonzalez E, Kulkarni H, Bolivar H, Mangano A, Sanchez R, et al: The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility. Science 307:1434-1440 (2005).
    • (2005) Science , vol.307 , pp. 1434-1440
    • Gonzalez, E.1    Kulkarni, H.2    Bolivar, H.3    Mangano, A.4    Sanchez, R.5
  • 13
    • 29444450702 scopus 로고    scopus 로고
    • Common deletions and SNPs are in linkage disequilibrium in the human genome
    • Hinds DA, Kloek AP, Jen M, Chen X, Frazer KA: Common deletions and SNPs are in linkage disequilibrium in the human genome. Nat Genet 38:82-85 (2006).
    • (2006) Nat Genet , vol.38 , pp. 82-85
    • Hinds, D.A.1    Kloek, A.P.2    Jen, M.3    Chen, X.4    Frazer, K.A.5
  • 15
    • 33745089349 scopus 로고    scopus 로고
    • Lafora progressive Myoclonus Epilepsy mutation database- EPM2A and NHLRC1 ( EMP2B ) genes
    • Ianzano L, Zhang J, Chan EM, Zhao XC, Lohi H, et al: Lafora progressive Myoclonus Epilepsy mutation database- EPM2A and NHLRC1 ( EMP2B ) genes. Hum Mutat 26:397 (2005).
    • (2005) Hum Mutat , vol.26 , pp. 397
    • Ianzano, L.1    Zhang, J.2    Chan, E.M.3    Zhao, X.C.4    Lohi, H.5
  • 16
    • 0037184794 scopus 로고    scopus 로고
    • Polymorphism of cytochrome P450 and xenobiotic toxicity
    • Ingelman-Sundberg M: Polymorphism of cytochrome P450 and xenobiotic toxicity. Toxicology 181-182:447-452 (2002).
    • (2002) Toxicology , vol.181-182 , pp. 447-452
    • Ingelman-Sundberg, M.1
  • 17
    • 0026495364 scopus 로고
    • Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors
    • Kallioniemi A, Kallioniemi OP, Sudar D, Rutovitz D, Gray JW, et al: Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors. Science 258:818-821 (1992).
    • (1992) Science , vol.258 , pp. 818-821
    • Kallioniemi, A.1    Kallioniemi, O.P.2    Sudar, D.3    Rutovitz, D.4    Gray, J.W.5
  • 18
    • 22844440839 scopus 로고    scopus 로고
    • Vive la difference!
    • Lee C: Vive la difference! Nat Genet 37:660-661 (2005).
    • (2005) Nat Genet , vol.37 , pp. 660-661
    • Lee, C.1
  • 20
    • 17344371740 scopus 로고    scopus 로고
    • High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays
    • Pinkel D, Segraves R, Sudar D, Clark S, Poole I, et al: High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays. Nat Genet 20:207-211 (1998).
    • (1998) Nat Genet , vol.20 , pp. 207-211
    • Pinkel, D.1    Segraves, R.2    Sudar, D.3    Clark, S.4    Poole, I.5
  • 22
    • 3242808027 scopus 로고    scopus 로고
    • Large-scale copy number polymorphism in the human genome
    • Sebat J, Lakshmi B, Troge J, Alexander J, Young J, et al: Large-scale copy number polymorphism in the human genome. Science 305:525-528 (2004).
    • (2004) Science , vol.305 , pp. 525-528
    • Sebat, J.1    Lakshmi, B.2    Troge, J.3    Alexander, J.4    Young, J.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.