메뉴 건너뛰기




Volumn 10, Issue 10, 2015, Pages

Virtual pharmacist: A platform for pharmacogenomics

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; COMPUTER PROGRAM; COMPUTER SECURITY; DATA PROCESSING; DRUG DATABASE; DRUG RESPONSE; EXOME; GENE SEQUENCE; GENOME; PHARMACIST; PHARMACOGENOMICS; SINGLE NUCLEOTIDE POLYMORPHISM; VARIANT CALL FORMAT; VIRTUAL PHARMACIST; WORKFLOW; COMPUTER INTERFACE; DATA MINING; GENOTYPE; HUMAN; HUMAN GENOME; INTERNET; MULTIVARIATE ANALYSIS; PERSONALIZED MEDICINE; PHARMACOGENETICS;

EID: 84949255994     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0141105     Document Type: Article
Times cited : (11)

References (29)
  • 3
    • 23044440450 scopus 로고    scopus 로고
    • The impact of CYP2C9 and VKORC1 genetic polymorphism and patient characteristics upon warfarin dose requirements: Proposal fora new dosing regimen
    • PMID: 15947090
    • Sconce EA, Khan TI, Wynne HA, Avery P, Monkhouse L, King BP, et al. The impact of CYP2C9 and VKORC1 genetic polymorphism and patient characteristics upon warfarin dose requirements: proposal fora new dosing regimen. Blood. 2005; 106(7):2329-33. PMID: 15947090
    • (2005) Blood. , vol.106 , Issue.7 , pp. 2329-2333
    • Sconce, E.A.1    Khan, T.I.2    Wynne, H.A.3    Avery, P.4    Monkhouse, L.5    King, B.P.6
  • 5
    • 79951809825 scopus 로고    scopus 로고
    • CPIC: Clinical pharmacogenetics implementation consortium of the pharmacogeno-mics research network
    • PMID: 21270786
    • Relling M, Klein T. CPIC: clinical pharmacogenetics implementation consortium of the pharmacogeno-mics research network. Clinical Pharmacology & Therapeutics. 2011; 89(3):464-7. doi: 10.1038/clpt. 2010.279 PMID: 21270786
    • (2011) Clinical Pharmacology & Therapeutics. , vol.89 , Issue.3 , pp. 464-467
    • Relling, M.1    Klein, T.2
  • 7
    • 33645072440 scopus 로고    scopus 로고
    • Gene sequencing. The raceforthe $1000 genome
    • Epub 2006/03/18 PMID: 16543431
    • Service RF. Gene sequencing. The raceforthe $1000 genome. Science. 2006; 311(5767):1544-6. Epub 2006/03/18. doi: 10.1126/science.311.5767.1544 PMID: 16543431.
    • (2006) Science. , vol.311 , Issue.5767 , pp. 1544-1546
    • Service, R.F.1
  • 8
    • 84886671743 scopus 로고    scopus 로고
    • The 'thousand-dollar genome': An ethical exploration
    • Epub 2013/05/17 PMID: 23677179; PubMed Central PMCID: PMCPmc3660958
    • Dondorp WJ, de Wert GM. The 'thousand-dollar genome': an ethical exploration. European journal of human genetics: EJHG. 2013; 21 Suppl 1:S6-26. Epub 2013/05/17. doi: 10.1038/ejhg.2013.73 PMID: 23677179; PubMed Central PMCID: PMCPmc3660958.
    • (2013) European Journal of Human Genetics: EJHG. , vol.21 , pp. S6-26
    • Dondorp, W.J.1    De Wert, G.M.2
  • 9
    • 33748923131 scopus 로고    scopus 로고
    • Sequencers step up to the speed challenge
    • Epub 2006/09/22 PMID: 16988678
    • Dalton R. Sequencers step up to the speed challenge. Nature. 2006; 443(7109):258-9. Epub 2006/09/22. doi: 10.1038/443258a PMID: 16988678.
    • (2006) Nature. , vol.443 , Issue.7109 , pp. 258-259
    • Dalton, R.1
  • 11
    • 77951589703 scopus 로고    scopus 로고
    • Clinical assessment incorporating a personal genome
    • PMID: 20435227
    • Ashley EA, Butte A. J., et al. Clinical assessment incorporating a personal genome. Lancet. 2010; 375 (9725):1525-35. doi: 10.1016/S0140-6736(10)60452-7 PMID: 20435227
    • (2010) Lancet. , vol.375 , Issue.9725 , pp. 1525-1535
    • Ashley, E.A.1    Butte, A.J.2
  • 12
    • 84864294140 scopus 로고    scopus 로고
    • WANNOVAR: Annotating genetic variants for personal genomes via the web
    • jmedgenet-2012-100918
    • Chang X, Wang K. wANNOVAR: annotating genetic variants for personal genomes via the web. Journal of medical genetics. 2012:jmedgenet-2012-100918.
    • (2012) Journal of Medical Genetics.
    • Chang, X.1    Wang, K.2
  • 14
    • 38049130261 scopus 로고    scopus 로고
    • Letting the Genome out of the Bottle-Will We Get Our Wish?
    • PMID: 18184955
    • Hunter DJ, Khoury MJ, Drazen JM. Letting the Genome out of the Bottle-Will We Get Our Wish? New England Journal of Medicine. 2008; 358(2):105-7. doi: 10.1056/NEJMp0708162 PMID: 18184955.
    • (2008) New England Journal of Medicine. , vol.358 , Issue.2 , pp. 105-107
    • Hunter, D.J.1    Khoury, M.J.2    Drazen, J.M.3
  • 16
    • 84904823994 scopus 로고    scopus 로고
    • The personal genome browser: Visualizing functions of genetic variants
    • Juan L, Teng M, Zang T, Hao Y, Wang Z, Yan C, et al. The personal genome browser: visualizing functions of genetic variants. Nucleic acids research. 2014; 42(W1):W192-W7.
    • (2014) Nucleic Acids Research. , vol.42 , Issue.W1 , pp. W192-W197
    • Juan, L.1    Teng, M.2    Zang, T.3    Hao, Y.4    Wang, Z.5    Yan, C.6
  • 17
    • 84904818189 scopus 로고    scopus 로고
    • A web-based interactive framework to assist in the prioritization of disease candidate genes in whole-exome sequencing studies
    • Alemán A, Garcia-Garcia F, Salavert F, Medina I, Dopazo J. A web-based interactive framework to assist in the prioritization of disease candidate genes in whole-exome sequencing studies. Nucleic acids research. 2014:gku407.
    • (2014) Nucleic Acids Research. , pp. gku407
    • Alemán, A.1    Garcia-Garcia, F.2    Salavert, F.3    Medina, I.4    Dopazo, J.5
  • 18
    • 78650775954 scopus 로고    scopus 로고
    • The $1, 000 genome, the $100, 000 analysis?
    • PMID: 21114804
    • Mardis E. The $1, 000 genome, the $100, 000 analysis? Genome Medicine. 2010; 2(11):84. doi: 10. 1186/gm205 PMID: 21114804
    • (2010) Genome Medicine. , vol.2 , Issue.11 , pp. 84
    • Mardis, E.1
  • 19
    • 77956534324 scopus 로고    scopus 로고
    • ANNOVAR: Functional annotation of genetic variants from high-throughput sequencing data
    • PMID: 20601685
    • Wang K, Li M, Hakonarson H.ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data. Nucleic acids research. 2010; 38(16):e164-e. doi: 10.1093/nar/gkq603 PMID: 20601685
    • (2010) Nucleic Acids Research. , vol.38 , Issue.16 , pp. e164-e
    • Wang, K.1    Li, M.2    Hakonarson, H.3
  • 20
    • 78650580271 scopus 로고    scopus 로고
    • GAMES identifies and annotates mutations in next-generation sequencing projects
    • PMID: 20971986
    • Sana ME, Iascone M, Marchetti D, Palatini J, Galasso M, Volinia S. GAMES identifies and annotates mutations in next-generation sequencing projects. Bioinformatics. 2011; 27(1):9-13. doi: 10.1093/bioinformatics/btq603 PMID: 20971986
    • (2011) Bioinformatics. , vol.27 , Issue.1 , pp. 9-13
    • Sana, M.E.1    Iascone, M.2    Marchetti, D.3    Palatini, J.4    Galasso, M.5    Volinia, S.6
  • 22
    • 78651287426 scopus 로고    scopus 로고
    • Drug Bank3.0: A comprehensive resource for 'omics' research on drugs
    • Knox C, Law V, Jewison T, Liu P, Ly S, Frolkis A, et al. Drug Bank3.0: a comprehensive resource for 'omics' research on drugs. Nucleic acids research. 2011; 39(suppl 1):D1035-D41.
    • (2011) Nucleic Acids Research. , vol.39 , pp. D1035-D1041
    • Knox, C.1    Law, V.2    Jewison, T.3    Liu, P.4    Ly, S.5    Frolkis, A.6
  • 23
    • 67649884743 scopus 로고    scopus 로고
    • Fast and accurate short read alignment with Burrows-Wheelertransform
    • PMID: 19451168
    • Li H, Durbin R. Fast and accurate short read alignment with Burrows-Wheelertransform. Bioinformatics. 2009; 25(14):1754-60. doi: 10.1093/bioinformatics/btp324 PMID: 19451168
    • (2009) Bioinformatics. , vol.25 , Issue.14 , pp. 1754-1760
    • Li, H.1    Durbin, R.2
  • 24
    • 68549104404 scopus 로고    scopus 로고
    • The sequence alignment/map format and SAMtools
    • PMID: 19505943
    • Li H, Handsaker B, Wysoker A, Fennell T, Ruan J, Homer N, et al. The sequence alignment/map format and SAMtools. Bioinformatics. 2009; 25(16):2078-9. doi: 10.1093/bioinformatics/btp352 PMID: 19505943
    • (2009) Bioinformatics. , vol.25 , Issue.16 , pp. 2078-2079
    • Li, H.1    Handsaker, B.2    Wysoker, A.3    Fennell, T.4    Ruan, J.5    Homer, N.6
  • 25
    • 77956295988 scopus 로고    scopus 로고
    • The Genome Analysis Toolkit: A Map Reduce framework for analyzing next-generation DNA sequencing data
    • Epub 2010/07/21 PMID: 20644199; PubMed Central PMCID: PMCPmc2928508
    • McKenna A, Hanna M, Banks E, Sivachenko A, Cibulskis K, Kernytsky A, et al. The Genome Analysis Toolkit: a Map Reduce framework for analyzing next-generation DNA sequencing data. Genome research. 2010; 20(9):1297-303. Epub 2010/07/21. doi: 10.1101/gr.107524.110 PMID: 20644199; PubMed Central PMCID: PMCPmc2928508.
    • (2010) Genome Research. , vol.20 , Issue.9 , pp. 1297-1303
    • McKenna, A.1    Hanna, M.2    Banks, E.3    Sivachenko, A.4    Cibulskis, K.5    Kernytsky, A.6
  • 26
    • 84975795680 scopus 로고    scopus 로고
    • An integrated map of genetic variation from 1, 092 human genomes
    • PMID: 23128226
    • Consortium GP. An integrated map of genetic variation from 1, 092 human genomes. Nature. 2012; 491 (7422):56-65. doi: 10.1038/nature11632 PMID: 23128226
    • (2012) Nature. , vol.491 , Issue.7422 , pp. 56-65
    • Consortium, G.P.1
  • 29
    • 84904793868 scopus 로고    scopus 로고
    • Disease Connect: A comprehensive web server for mechanism-based disease-disease connections
    • Liu C-C, Tseng Y-T, Li W, Wu C-Y, Mayzus I, Rzhetsky A, et al. Disease Connect: a comprehensive web server for mechanism-based disease-disease connections. Nucleic acids research. 2014; 42 (W1):W137-W46.
    • (2014) Nucleic Acids Research. , vol.42 , Issue.W1 , pp. W137-W146
    • Liu, C.-C.1    Tseng, Y.-T.2    Li, W.3    Wu, C.-Y.4    Mayzus, I.5    Rzhetsky, A.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.