High-throughput electronic biology: mining information for drug discovery

被引:63
作者
Loging, William [1 ]
Harland, Lee
Williams-Jones, Bryn
机构
[1] Pfizer Inc, Computat Biol Grp, Groton, CT 06340 USA
[2] Pfizer Ltd, eBiol Grp, Sandwich CT13 9NJ, Kent, England
[3] Pfizer Ltd, Computat Biol Grp, Sandwich CT13 9NJ, Kent, England
关键词
D O I
10.1038/nrd2265
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The vast range of in silico resources that are available in life sciences research hold much promise towards aiding the drug discovery process. To fully realize this opportunity, computational scientists must consider the practical issues of data integration and identify how best to apply these resources scientifically. In this article we describe in silico approaches that are driven towards the identification of testable laboratory hypotheses; we also address common challenges in the field. We focus on flexible, high-throughput techniques, which may be initiated independently of 'wet-lab' experimentation, and which may be applied to multiple disease areas. The utility of these approaches in drug discovery highlights the contribution that in silico techniques can make and emphasizes the need for collaboration between the areas of disease research and computational science.
引用
收藏
页码:220 / 230
页数:11
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