An assessment of Motorola CodeLink™ microarray performance for gene expression profiling applications -: art. no. e30

被引:153
作者
Ramakrishnan, R [1 ]
Dorris, D [1 ]
Lublinsky, A [1 ]
Nguyen, A [1 ]
Domanus, M [1 ]
Prokhorova, A [1 ]
Gieser, L [1 ]
Touma, E [1 ]
Lockner, R [1 ]
Tata, M [1 ]
Zhu, XM [1 ]
Patterson, M [1 ]
Shippy, R [1 ]
Sendera, TJ [1 ]
Mazumder, A [1 ]
机构
[1] Motorola Life Sci, Northbrook, IL 60062 USA
关键词
D O I
10.1093/nar/30.7.e30
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
DNA microarrays enable users to obtain information on differences in transcript abundance on a massively parallel scale. Recently, however, data analyses have revealed potential pitfalls related to image acquisition, variability and misclassifications in replicate measurements, cross-hybridization and sensitivity limitations. We have generated a series of analytical tools to address the manufacturing, detection and data analysis components of a microarray experiment. Together, we have used these tools to optimize performance in an expression profiling study. We demonstrate three significant advantages of the Motorola CodeLink(TM) platform: sensitivity of one copy per cell, coefficients of variation of 10% in the hybridization signals across slides and across target preparations, and specificity in distinguishing highly homologous sequences. Slides where oligonucleotide probes are spotted in 6-fold redundancy were used to demonstrate the effect of replication on data quality. Lastly, the differential expression ratios obtained with the CodeLink(TM) expression platform were validated against those obtained with quantitative reverse transcription-PCR assays for 54 genes.
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页数:12
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