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Volumn 41, Issue D1, 2013, Pages

DbVar and DGVa: Public archives for genomic structural variation

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; COMPUTER INTERFACE; COMPUTER PROGRAM; COMPUTER SYSTEM; COPY NUMBER VARIATION; DATA ANALYSIS SOFTWARE; DBVAR DATABASE; DGVA DATABASE; GENE SEQUENCE; GENETIC DATABASE; GENETIC VARIABILITY; PHENOTYPE; PRIORITY JOURNAL; PROCESS DEVELOPMENT; REFERENCE DATABASE; VALIDATION PROCESS;

EID: 84876527890     PISSN: 03051048     EISSN: 13624962     Source Type: Journal    
DOI: 10.1093/nar/gks1213     Document Type: Article
Times cited : (209)

References (20)
  • 5
    • 79954672317 scopus 로고    scopus 로고
    • Genome structural variation discovery and genotyping
    • Alkan, C., Coe, B.P. and Eichler, E.E. (2011) Genome structural variation discovery and genotyping. Nat. Rev. Genet., 12, 363-376.
    • (2011) Nat. Rev. Genet. , vol.12 , pp. 363-376
    • Alkan, C.1    Coe, B.P.2    Eichler, E.E.3
  • 7
    • 84975742565 scopus 로고    scopus 로고
    • A map of human genome variation from population-scale sequencing
    • Durbin, R. (2010) A map of human genome variation from population-scale sequencing. Nature, 467, 1061-1073.
    • (2010) Nature , vol.467 , pp. 1061-1073
    • Durbin, R.1
  • 13
  • 14
    • 77953936166 scopus 로고    scopus 로고
    • The human phenotype ontology
    • Robinson, P.N. and Mundlos, S. (2010) The human phenotype ontology. Clinical genetics, 77, 525-534.
    • (2010) Clinical Genetics , vol.77 , pp. 525-534
    • Robinson, P.N.1    Mundlos, S.2
  • 18
    • 33751527925 scopus 로고    scopus 로고
    • Development of bioinformatics resources for display and analysis of copy number and other structural variants in the human genome
    • Zhang, J., Feuk, L., Duggan, G.E., Khaja, R. and Scherer, S.W. (2006) Development of bioinformatics resources for display and analysis of copy number and other structural variants in the human genome. Cytogenet. Genome Res., 115, 205-214.
    • (2006) Cytogenet. Genome Res. , vol.115 , pp. 205-214
    • Zhang, J.1    Feuk, L.2    Duggan, G.E.3    Khaja, R.4    Scherer, S.W.5
  • 20
    • 77955405475 scopus 로고    scopus 로고
    • Deriving the consequences of genomic variants with the Ensembl API and SNP effect predictor
    • McLaren, W., Pritchard, B., Rios, D., Chen, Y., Flicek, P. and Cunningham, F. (2010) Deriving the consequences of genomic variants with the Ensembl API and SNP effect predictor. Bioinformatics, 26, 2069-2070.
    • (2010) Bioinformatics , vol.26 , pp. 2069-2070
    • McLaren, W.1    Pritchard, B.2    Rios, D.3    Chen, Y.4    Flicek, P.5    Cunningham, F.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.