Comparative microarray analysis

被引:41
作者
Larsson, Ola
Wennmalm, Kristian
Sandberg, Rickard
机构
[1] Univ Minnesota, Dept Med, Minneapolis, MN 55455 USA
[2] Karolinska Inst, Ctr Canc, Dept Pathol & Oncol, Stockholm, Sweden
[3] St Gorans Univ Hosp, S-11281 Stockholm, Sweden
[4] MIT, Dept Biol, Cambridge, MA 02139 USA
关键词
D O I
10.1089/omi.2006.10.381
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
Microarrays enable high-throughput parallel gene expression analysis, and their use has grown exponentially during the past decade. We are now in a position where individual experiments could benefit from using the swelling public data repositories to allow microarrays to progress from being a hypothesis-generating tool to a powerful resource that can be used to test hypothesis about biology. Comparative microarray analysis could better distinguish phenotypes from associated phenotypes; identify valid differentially expressed genes by combining many studies; test new hypothesis; and discover fundamental patterns of gene regulation. This review aims to describe the additional methodology needed for such comparative microarray analysis, and we identify and discuss a number of problems such as loss of published data, lack of annotations, and variable array quality, which need to be solved before comparative microarray analysis can be used in a more systematic and powerful manner.
引用
收藏
页码:381 / 397
页数:17
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