首页> 外文期刊>DNA research: an international journal for rapid publication of reports on genes and genomes >Detection and normalization of biases present in spotted cDNA microarray data: a composite method addressing dye, intensity-dependent, spatially-dependent, and print-order biases.
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Detection and normalization of biases present in spotted cDNA microarray data: a composite method addressing dye, intensity-dependent, spatially-dependent, and print-order biases.

机译:斑点cDNA微阵列数据中存在的偏差的检测和归一化:一种解决染料,强度依赖性,空间依赖性和打印顺序偏差的复合方法。

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摘要

Microarrays are often used to identify target genes that trigger specific diseases, to elucidate the mechanisms of drug effects, and to check SNPs. However, data from microarray experiments are well known to contain biases resulting from the experimental protocols. Therefore, in order to elucidate biological knowledge from the data, systematic biases arising from their protocols must be removed prior to any data analysis. To remove these biases, many normalization methods are used by researchers. However, not all biases are eliminated from the microarray data because not all types of errors from experimental protocols are known. In this paper, we report an effective way of removing various types of biases by treating each microarray dataset independently to detect biases present in the dataset. After the biases contained in each dataset were identified, a combination of normalization methods specifically made for each dataset was applied to remove biases one at a time.
机译:微阵列通常用于鉴定触发特定疾病的靶基因,阐明药物作用的机制并检查SNP。但是,众所周知,来自微阵列实验的数据包含实验方案产生的偏差。因此,为了从数据中阐明生物学知识,在进行任何数据分析之前,必须消除由于其规程引起的系统性偏见。为了消除这些偏差,研究人员使用了许多标准化方法。然而,由于并非所有来自实验方案的错误类型,都无法从微阵列数据中消除所有偏差。在本文中,我们报告了一种通过独立处理每个微阵列数据集以检测数据集中存在的偏差来消除各种类型偏差的有效方法。识别每个数据集中包含的偏差后,将针对每个数据集专门制定的归一化方法组合应用于一次消除一个偏差。

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