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Volumn 40, Issue D1, 2012, Pages

SNPedia: A wiki supporting personal genome annotation, interpretationand analysis

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOMATION; COMPUTER PROGRAM; GENE FREQUENCY; GENE LOCUS; GENETIC ASSOCIATION; GENETIC DATABASE; GENETIC VARIABILITY; GENOME; GENOTYPE; HETEROZYGOSITY; HOMOZYGOSITY; NOMENCLATURE; PHENOTYPE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; SNPEDIA DATABASE;

EID: 84861063896     PISSN: 03051048     EISSN: 13624962     Source Type: Journal    
DOI: 10.1093/nar/gkr798     Document Type: Article
Times cited : (174)

References (11)
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    • DOI 10.1093/nar/gki033
    • Hamosh,A., Scott,A., Amberger,J., Bocchini,C. and McKusick,V. (2005) Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders. Nucleic Acids Res., 33, D514-D517. (Pubitemid 40207927)
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    • Hamosh, A.1    Scott, A.F.2    Amberger, J.S.3    Bocchini, C.A.4    McKusick, V.A.5
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    • The personal genome project
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    • Davies, K.1
  • 11
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    • Structural variation in two human genomes mapped at single-nucleotide resolution by whole genome de novo assembly
    • Li,Y., Zheng,H., Luo,R., Wu,H., Zhu,H., Li,R., Cao,H., Wu,B., Huang,S., Shao,H. et al. (2011) Structural variation in two human genomes mapped at single-nucleotide resolution by whole genome de novo assembly. Nat. Biotech., 29, 723-730.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.