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Volumn 18, Issue 1, 2017, Pages

Accurate and equitable medical genomic analysis requires an understanding of demography and its influence on sample size and ratio

Author keywords

[No Author keywords available]

Indexed keywords

AFRICAN; ANCESTRY GROUP; ASIAN; DEMOGRAPHY; ETHNIC DIFFERENCE; EUROPEAN; GENE FREQUENCY; GENETIC VARIABILITY; GENOME ANALYSIS; HISPANIC; HUMAN; LETTER; POPULATION DISTRIBUTION; POPULATION SIZE; ETHNIC GROUP; GENOMICS; PROCEDURES; REPRODUCIBILITY; SAMPLE SIZE; STANDARDS;

EID: 85014128406     PISSN: 14747596     EISSN: 1474760X     Source Type: Journal    
DOI: 10.1186/s13059-017-1172-8     Document Type: Letter
Times cited : (2)

References (8)
  • 1
    • 84979523711 scopus 로고    scopus 로고
    • Unequal representation of genetic variation across ancestry groups creates healthcare inequality in the application of precision medicine
    • Petrovski S, Goldstein DB. Unequal representation of genetic variation across ancestry groups creates healthcare inequality in the application of precision medicine. Genome Biol. 2016;17:157.
    • (2016) Genome Biol , vol.17 , pp. 157
    • Petrovski, S.1    Goldstein, D.B.2
  • 2
    • 84946081339 scopus 로고    scopus 로고
    • OMIM.org: Online Mendelian Inheritance in Man (OMIM(R)), an online catalog of human genes and genetic disorders
    • Amberger JS, Bocchini CA, Schiettecatte F, Scott AF, Hamosh A. OMIM.org: Online Mendelian Inheritance in Man (OMIM(R)), an online catalog of human genes and genetic disorders. Nucleic Acids Res. 2015;43:D789-98.
    • (2015) Nucleic Acids Res , vol.43 , pp. D789-D798
    • Amberger, J.S.1    Bocchini, C.A.2    Schiettecatte, F.3    Scott, A.F.4    Hamosh, A.5
  • 4
    • 84863556835 scopus 로고    scopus 로고
    • Evolution and functional impact of rare coding variation from deep sequencing of human exomes
    • Tennessen JA, Bigham AW, O'Connor TD, Fu W, Kenny EE, Gravel S, et al. Evolution and functional impact of rare coding variation from deep sequencing of human exomes. Science. 2012;337:64-9.
    • (2012) Science , vol.337 , pp. 64-69
    • Tennessen, J.A.1    Bigham, A.W.2    O'Connor, T.D.3    Fu, W.4    Kenny, E.E.5    Gravel, S.6
  • 5
    • 84872143942 scopus 로고    scopus 로고
    • Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants
    • Fu W, O'Connor TD, Jun G, Kang HM, Abecasis G, Leal SM, et al. Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants. Nature. 2013;493:216-20.
    • (2013) Nature , vol.493 , pp. 216-220
    • Fu, W.1    O'Connor, T.D.2    Jun, G.3    Kang, H.M.4    Abecasis, G.5    Leal, S.M.6
  • 8
    • 84991409036 scopus 로고    scopus 로고
    • Challenges and disparities in the application of personalized genomic medicine to populations with African ancestry
    • Kessler MD, Yerges-Armstrong L, Taub MA, Shetty AC, Maloney K, Jeng LJ, et al. Challenges and disparities in the application of personalized genomic medicine to populations with African ancestry. Nat Commun. 2016;7:12521.
    • (2016) Nat Commun , vol.7 , pp. 12521
    • Kessler, M.D.1    Yerges-Armstrong, L.2    Taub, M.A.3    Shetty, A.C.4    Maloney, K.5    Jeng, L.J.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.