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Volumn 57, Issue 10, 2012, Pages 676-678

NDesign: Software for study design for the detection of rare variants from next-generation sequencing data

Author keywords

next generation sequencing; rare variant detection; study design

Indexed keywords

ALLELE; ARTICLE; COMPUTER LANGUAGE; COMPUTER PROGRAM; GENE SEQUENCE; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC VARIABILITY; HETEROZYGOTE; INTERNET; NEXT GENERATION SEQUENCING; WEB BROWSER;

EID: 84867972906     PISSN: 14345161     EISSN: 1435232X     Source Type: Journal    
DOI: 10.1038/jhg.2012.81     Document Type: Article
Times cited : (3)

References (8)
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    • (2002) Nat. Genet , vol.32 , pp. 650-654
    • Ozaki, K.1    Ohnishi, Y.2    Iida, A.3    Sekine, A.4    Yamada, R.5    Tsunoda, T.6
  • 2
    • 20244380171 scopus 로고    scopus 로고
    • Complement factor H polymorphism in age-related macular degeneration
    • Klein, R, J., Zeiss, C., Chew, E. Y., Tsai, J. K., Sackler, R. S., Haynes, C. et al. Complement factor H polymorphism in age-related macular degeneration. Science 308, 385-389 (2005
    • (2005) Science , vol.308 , pp. 385-389
    • Klein, R.J.1    Zeiss, C.2    Chew, E.Y.3    Tsai, J.K.4    Sackler, R.S.5    Haynes, C.6
  • 3
    • 33845340501 scopus 로고    scopus 로고
    • A genome-wide association study identifies IL23R as an inflammatory bowel disease gene
    • Duerr, R, H., Taylor, K. D., Brant, S. R., Rioux, J. D., Silverberg, M. S., Daly, M. J. et al. A genome-wide association study identifies IL23R as an inflammatory bowel disease gene. Science 314, 1461-1463 (2006
    • (2006) Science , vol.314 , pp. 1461-1463
    • Duerr, R.H.1    Taylor, K.D.2    Brant, S.R.3    Rioux, J.D.4    Silverberg, M.S.5    Daly, M.J.6
  • 4
    • 33846627302 scopus 로고    scopus 로고
    • A genomewide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1
    • Hampe, J., Franke, A., Rosenstiel, P., Till, A., Teuber, M., Huse, K. et al. A genomewide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1. Nat. Genet. 39, 207-211 (2006
    • (2006) Nat. Genet , vol.39 , pp. 207-211
    • Hampe, J.1    Franke, A.2    Rosenstiel, P.3    Till, A.4    Teuber, M.5    Huse, K.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.