eMERGEing progress in genomics-the first seven years.

eMERGEing progress in genomics-the first seven years.
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DOI:
10.3389/fgene.2014.00184
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发表时间:
2014
影响因子:
3.7
通讯作者:
Ritchie MD
Ritchie MD
中科院分区:
生物学3区
文献类型:
--
作者:
Crawford DC;Crosslin DR;Tromp G;Kullo IJ;Kuivaniemi H;Hayes MG;Denny JC;Bush WS;Haines JL;Roden DM;McCarty CA;Jarvik GP;Ritchie MD

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电子病历和基因组学 (eMERGE) 网络由美国国立卫生研究院 (NIH) 的国家人类基因组研究所 (NHGRI) 于 2007 年建立,部分目的是探索电子病历 (EMR) 在基因组科学中的实用性。最初的重点是主要使用全基因组关联范式进行发现,但最近,该网络已开始评估将新基因组信息与临床决策支持结合到 EMR 中的机制。在此,我们描述了这一演变,包括个体和合并的 eMERGE 基因组数据集的开发、网络对基因组发现和人类健康所做的贡献,以及为下一代基因型-表型关联研究和临床实施所采取的步骤。
The electronic MEdical Records & GEnomics (eMERGE) network was established in 2007 by the National Human Genome Research Institute (NHGRI) of the National Institutes of Health (NIH) in part to explore the utility of electronic medical records (EMRs) in genome science. The initial focus was on discovery primarily using the genome-wide association paradigm, but more recently, the network has begun evaluating mechanisms to implement new genomic information coupled to clinical decision support into EMRs. Herein, we describe this evolution including the development of the individual and merged eMERGE genomic datasets, the contribution the network has made toward genomic discovery and human health, and the steps taken toward the next generation genotype-phenotype association studies and clinical implementation.
来自1,092个人基因组的遗传变异的综合图。
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