Development of a large-scale de-identified DNA biobank to enable personalized medicine

被引:669
作者
Roden, D. M. [1 ,2 ,3 ]
Pulley, J. M. [4 ]
Basford, M. A. [1 ,4 ]
Bernard, G. R. [2 ,4 ]
Clayton, E. W. [5 ,6 ]
Balser, J. R. [3 ,4 ]
Masys, D. R. [7 ]
机构
[1] Vanderbilt Univ, Sch Med, Off Personalized Med, Nashville, TN 37212 USA
[2] Vanderbilt Univ, Sch Med, Dept Med, Nashville, TN 37212 USA
[3] Vanderbilt Univ, Sch Med, Dept Pharmacol, Nashville, TN 37212 USA
[4] Vanderbilt Univ, Sch Med, Res Off, Nashville, TN 37212 USA
[5] Vanderbilt Univ, Sch Med, Dept Pediat, Nashville, TN 37212 USA
[6] Vanderbilt Univ, Sch Law, Nashville, TN 37212 USA
[7] Vanderbilt Univ, Sch Med, Dept Biomed Informat, Nashville, TN 37212 USA
关键词
D O I
10.1038/clpt.2008.89
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Our objective was to develop a DNA biobank linked to phenotypic data derived from an electronic medical record (EMR) system. An "opt-out" model was implemented after significant review and revision. The plan included (i) development and maintenance of a de-identified mirror image of the EMR, namely, the "synthetic derivative" (SD) and (ii) DNA extracted from discarded blood samples and linked to the SD. Surveys of patients indicated general acceptance of the concept, with only a minority (similar to 5%) opposing it. As a result, mechanisms to facilitate opt-out included publicity and revision of a standard "consent to treatment" form. Algorithms for sample handling and procedures for de-identification were developed and validated in order to ensure acceptable error rates (<0.3 and <0.1%, respectively). The rate of sample accrual is 700-900 samples/week. The advantages of this approach are the rate of sample acquisition and the diversity of phenotypes based on EMRs.
引用
收藏
页码:362 / 369
页数:8
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