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Volumn 18, Issue SUPPL. 2, 2002, Pages

A similarity-based method for genome-wide prediction of disease-relevant human genes

Author keywords

[No Author keywords available]

Indexed keywords

CONFERENCE PAPER; DATA BASE; DISEASE CLASSIFICATION; GENE FUNCTION; GENE LOCUS; GENE MUTATION; GENE TARGETING; GENETIC DISORDER; HUMAN; HUMAN GENOME; MONOGENIC DISORDER; PHENOTYPE; PREDICTION; PRIORITY JOURNAL; VALIDATION PROCESS;

EID: 0037580196     PISSN: 13674803     EISSN: 13674811     Source Type: Journal    
DOI: 10.1093/bioinformatics/18.suppl_2.S110     Document Type: Conference Paper
Times cited : (194)

References (11)
  • 1
    • 2042437650 scopus 로고    scopus 로고
    • Initial Sequencing and Analysis of the Human Genome
    • International Human Genome Sequencing Consortium (2001) Initial Sequencing and Analysis of the Human Genome. Nature, 409, 860-921.
    • (2001) Nature , vol.409 , pp. 860-921
  • 2
    • 0035895505 scopus 로고    scopus 로고
    • The sequence of the human genome
    • Venter,J.C. et al. (2001) The sequence of the human genome. Science, 291, 1304-1351.
    • (2001) Science , vol.291 , pp. 1304-1351
    • Venter, J.C.1
  • 3
    • 0028877463 scopus 로고
    • Genetic dissection of complex traits: Guidelines for interpreting and reporting linkage results
    • Lander,E. and Kruglyak,L. (1995) Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results. Nature Genet., 11, 241-247.
    • (1995) Nature Genet. , vol.11 , pp. 241-247
    • Lander, E.1    Kruglyak, L.2
  • 4
    • 0029741063 scopus 로고    scopus 로고
    • The future of genetic studies of complex human disease
    • Risch,N. and Merikangas,K. (1996) The future of genetic studies of complex human disease. Science, 273, 1516-1517.
    • (1996) Science , vol.273 , pp. 1516-1517
    • Risch, N.1    Merikangas, K.2
  • 5
    • 0036649742 scopus 로고    scopus 로고
    • Association of genes to genetically inherited diseases using data mining
    • June 2002 advance online publication
    • Perez-Iratxeta,C. et al. (2002) Association of genes to genetically inherited diseases using data mining. Nature Genet., (June 2002 advance online publication).
    • (2002) Nature Genet.
    • Perez-Iratxeta, C.1
  • 6
    • 0033985936 scopus 로고    scopus 로고
    • Online Mendelian Inheritance in Man (OMIM)
    • Hamosh,A. et al. (2000) Online Mendelian Inheritance in Man (OMIM). Human Mutation, 15, 57-61.
    • (2000) Human Mutation , vol.15 , pp. 57-61
    • Hamosh, A.1
  • 7
    • 0035175625 scopus 로고    scopus 로고
    • Proteome analysis database: Online application of InterPro and ClusSTr for the functional classification of proteins in whole genomes
    • Apweiler,R. et al. (2001) Proteome analysis database: online application of InterPro and ClusSTr for the functional classification of proteins in whole genomes. Nucleic Acids Res., 29, 44-48.
    • (2001) Nucleic Acids Res. , vol.29 , pp. 44-48
    • Apweiler, R.1
  • 8
    • 0034069495 scopus 로고    scopus 로고
    • Gene Ontology: Tool for the unification of biology
    • The Gene Ontology Consortium (2000) Gene Ontology: tool for the unification of biology. Nature Genet., 25, 25-29.
    • (2000) Nature Genet. , vol.25 , pp. 25-29
  • 9
    • 0035865078 scopus 로고    scopus 로고
    • Human disease genes
    • Jiminez-Sanchez,G. et al. (2001) Human disease genes. Nature, 409, 853-854.
    • (2001) Nature , vol.409 , pp. 853-854
    • Jiminez-Sanchez, G.1
  • 10
    • 33544457003 scopus 로고    scopus 로고
    • An automated computer system to support ultra high throughput SNP genotyping
    • Heil,A. et al. (2002) An automated computer system to support ultra high throughput SNP genotyping. Pac. Symp. Biocomput., 7, 41-52.
    • (2002) Pac. Symp. Biocomput. , vol.7 , pp. 41-52
    • Heil, A.1


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