Quantitative polymerase chain reaction: Validation of microarray results from postmortem brain studies

被引:40
|
作者
Mimmack, ML
Brooking, J
Bahn, S [1 ]
机构
[1] Babraham Inst, Dept Neurobiol, Cambridge CB2 4AT, England
[2] Babraham Inst, Med Res Council Geneserv, Cambridge CB2 4AT, England
[3] Babraham Inst, Babraham Bioincubator, Cambridge CB2 4AT, England
[4] Univ Cambridge, Addenbrookes Hosp, Dept Psychiat, Cambridge CB2 1TN, England
关键词
quantitative polymerase chain reaction (Q-PCR); reverse transcription polymerase chain reaction (RT-PCR); minor groove binder; standard curve analysis; housekeeping genes; dissociation curve analysis;
D O I
10.1016/j.biopsych.2003.09.007
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Quantitative polymerase chain reaction (Q-PCR) is now considered the "technique of choice" for validating gene expression changes identified with ribonucleic acid-based expression profiling technologies (especially micro- and macroarray techniques). The identification of altered gene expression profiles with microarrays is best viewed as the first step in the determination of potential disease-associated genes; however, the false-positive rate can be high, particularly with small sample sets and in view of the typically small differences observed in brain expression studies. Quantitative PCR is a rapid and highly sensitive technique for accurate quantification of microarray results; however, careful consideration of experimental design, quality of primer/probe design, internal standards, and normalization procedures are pivotal, particularly when the work involves postmortem tissue.
引用
收藏
页码:337 / 345
页数:9
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