Genomic data sharing for translational research and diagnostics

被引：6
|
作者：
Robinson, Peter N. [1 ,2 ,3 ,4 ]
机构：
[1] Charite, Inst Med & Human Genet, D-13353 Berlin, Germany
[2] Charite, Berlin Ctr Regenerat Therapies, D-13353 Berlin, Germany
[3] Max Planck Inst Mol Genet, D-14195 Berlin, Germany
[4] Free Univ Berlin, Dept Math & Comp Sci, Inst Bioinformat, D-14195 Berlin, Germany
来源：
GENOME MEDICINE | 2014年 / 6卷
关键词：
MISSING HERITABILITY; HUMAN PHENOTYPE; SEQUENCE;
D O I：
10.1186/s13073-014-0078-2
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
Translational genomics is changing, not only in the technology used but also in the sharing of data. The enormous potential for genomics technologies to improve patient care has been recognized, but it will not be reached unless powerful but secure data-sharing technologies are developed. A recent study demonstrates the power of federated queries, in which sequence variants can be searched simultaneously in files distributed over multiple centers.
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页数：3
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