Update: looking beyond the 100,000 Genome Project

被引：5
|
作者：
Haga, Susanne B. [1 ]
机构：
[1] Duke Univ, Sch Med, Ctr Appl Genom & Precis Med, 304 Res Dr,Box 90141, Durham, NC 27708 USA
来源：
PERSONALIZED MEDICINE | 2017年 / 14卷 / 02期
关键词：
big data; clinical implementation; communication; patient engagement; provider training; sequencing; PRECISION MEDICINE; HEALTHY-INDIVIDUALS; SEQUENCING PANEL; CANCER-RISK; SCIENCE; ADULT; CARE;
D O I：
10.2217/pme-2016-0101
中图分类号：
R9 [药学];
学科分类号：
1007 ;
摘要：
Though the idea of incorporating genomic data in health risk assessments has been raised, the benefits of universal-genome sequencing are far from clear in healthy patients, and even for some diseases.
引用
收藏
页码：85 / 87
页数：3
相关论文
共 50 条
  • [21] GENOMICS ENGLAND'S 100,000 GENOME PROJECT: WHERE DO BRAIN TUMOURS FIT IN?
    Ashkan, Keyoumars
    Houlston, Richard
    NEURO-ONCOLOGY, 2017, 19 : 124 - 124
  • [22] 100,000 genomes project: Integrating whole genome sequencing (WGS) data into clinical practice
    Sosinsky, A.
    Ambrose, J.
    Zarowiecki, M.
    Mitchell, J.
    Henderson, S.
    Murugaesu, N.
    Hamblin, A.
    Turnbull, C.
    Walker, S.
    Perez-Gil, D.
    Rueda-Martin, A.
    Fowler, T.
    Caulfield, M.
    Rendon, A.
    ANNALS OF ONCOLOGY, 2019, 30
  • [23] A pipeline to detect repeat expansions from whole genome sequencing in the 100,000 Genomes Project
    Ibanez, K.
    Dolzhenko, E.
    Smith, K. R.
    Scott, R. H.
    Thomas, E.
    Baple, E.
    Brittain, H.
    Bourn, D.
    Brennan, P.
    Polke, J.
    Houlden, H.
    Rendon, A.
    Caulfield, M. J.
    Eberle, M. A.
    Tucci, A.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 : 847 - 848
  • [24] 100,000 Men
    Foofo, Fafa
    TRANSITION, 2015, (117) : 91 - 98
  • [25] PROJECT-100,000
    BRADDOCK, C
    PHI DELTA KAPPAN, 1967, 48 (09) : 425 - 427
  • [26] 100,000 Tons Primary Aluminum Project at Mianchi County
    China Nonferrous Metals Monthly, 2002, (05) : 5 - 5
  • [27] 100,000 Days
    不详
    BULLETIN OF THE MENNINGER CLINIC, 1939, 3 (04) : 127 - 127
  • [28] Participant experiences of genome sequencing for rare diseases in the 100,000 Genomes Project: A mixed methods study
    Peter, Michelle
    Hammond, Jennifer
    Sanderson, Saskia C.
    Gurasashvili, Jana
    Hunter, Amy
    Searle, Beverly
    Patch, Christine
    Chitty, Lyn S.
    Hill, Melissa
    Lewis, Celine
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2022, 30 (SUPPL 1) : 69 - 69
  • [29] 100,000 collaborators
    Lefebvre, Denis
    HISTORIA, 2017, (850): : 16 - 17
  • [30] The NHS England 100,000 Genomes Project: feasibility and utility of centralised genome sequencing for children with cancer
    Jamie Trotman
    Ruth Armstrong
    Helen Firth
    Claire Trayers
    James Watkins
    Kieren Allinson
    Thomas S. Jacques
    James C. Nicholson
    G. A. Amos Burke
    Sam Behjati
    Matthew J. Murray
    Catherine E. Hook
    Patrick Tarpey
    British Journal of Cancer, 2022, 127 : 137 - 144
12345