Technical evaluation of cDNA microarrays.

APMIS. Supplementum Pub Date : 2003-01-01
Casper M Frederiksen, Mads Aaboe, Lars Dyrskjøt, Søren Laurberg, Hans Wolf, Torben F Ørntoft, Mogens Kruhøffer
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Abstract

The aims were to evaluate the common reference design approach in microarray experiments and to evaluate the technical performance and the normalisation of cDNA microarrays with a limited number of spots. Total RNA from 3 normal and 3 tumour sample biopsies were used for synthesis of amino-allyl labelled cRNA. Equal amounts of cRNA from all samples were mixed as reference. After conjugation of cRNA with fluorophores (Cy3/Cy5), each individual tumour cRNA was hybridised to a cDNA microarray together with reference cRNA, scanned and analysed. We show that our procedures for producing cDNA microarrays are reproducible. The concordance between duplicated spots and replicate hybridisation was found to be high. We have demonstrated that our cDNA microarrays are of a high technical quality. The majority of the cDNA microarrays had low local spot background levels. Despite the high background levels for some local spots, variation could be minimized by locally weighted scatter plot smooth normalisation (LOWESS), which we showed was also suitable for normalisation of cDNA microarrays with a limited number of probes.

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cDNA微阵列技术评价。
目的是评估微阵列实验中常见的参考设计方法,并评估具有有限数量斑点的cDNA微阵列的技术性能和规范化。3个正常和3个肿瘤活检样本的总RNA用于合成氨基烯丙基标记的cRNA。将所有样本中等量的cRNA混合作为参考。将cRNA与荧光团(Cy3/Cy5)偶联后,将每个肿瘤cRNA与参考cRNA杂交到cDNA微阵列中,进行扫描和分析。我们表明,我们的程序生产cDNA微阵列是可重复的。重复点与重复杂交的一致性较高。我们已经证明了我们的cDNA微阵列具有很高的技术质量。大多数cDNA微阵列具有较低的局部斑点背景水平。尽管某些局部斑点的背景水平很高,但通过局部加权散点图平滑归一化(LOWESS)可以将变异最小化,我们发现该方法也适用于具有有限数量探针的cDNA微阵列的归一化。
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