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DNA probe signal processing for identification of abnormal gene regulation and pathogenetic understanding — A data mining approach

机译:DNA探针信号处理,用于识别异常基因调控和病原学理解—一种数据挖掘方法

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Gene expression microarray leverages DNA probes to acquire signal intensity in the hybridized biological samples, and has become a major source for producing high-throughput experiment data. The raw, probe-level signal leads to a comprehensive understanding of the overall microarray data set, which is especially useful when the goals of the research are different from the original data producer or contributor. Dissecting the genetic basis of complex diseases and understanding their pathogenesis thereby hinges on the successful processing of the DNA probe-level signal. Moreover, starting exploration from raw probe-level signal ensures the integrity of original data from being compromized, thus usually yielding reasonable instinct towards choosing the precise algorithms or techniques for further analysis. In this paper, we present steps towards processing probe-level signal from the microarray. As case studies of our approach, two public data sets are then used, starting from scratch: one describes the gene expression in synchronous and metachronous liver metastatic lesions from colorectal cancer, the other one uses biopsies from patients with EBV-positive undifferentiated nasopharyngeal carcinoma and from cancer-free controls. Compared with previous work, our approach not only identifies up/ down-regulated genes, but discovers insightful pathogenesis as well.
机译:基因表达微阵列利用DNA探针获取杂交生物样品中的信号强度,已成为产生高通量实验数据的主要来源。原始的探针级信号可导致对整个微阵列数据集的全面了解,这在研究目标与原始数据产生者或贡献者不同的情况下尤其有用。剖析复杂疾病的遗传基础并了解其发病机理,取决于DNA探针水平信号的成功处理。此外,从原始探针级信号开始探索可确保原始数据的完整性不受影响,因此通常会产生合理的本能,以选择进一步分析的精确算法或技术。在本文中,我们介绍了处理来自微阵列的探针水平信号的步骤。作为我们方法的案例研究,从头开始使用了两个公共数据集:一个描述了结直肠癌同步和异时肝转移病灶中的基因表达,另一个描述了EBV阳性未分化鼻咽癌患者的活检样本,以及来自无癌症的对照。与以前的工作相比,我们的方法不仅可以识别上调/下调的基因,而且还可以发现有洞察力的发病机理。

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