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Gene Expression Signature Discovery using Independent Component Analysis

机译:基因表达签名发现使用独立分量分析

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With the advent of high throughput DNA microarrays and the large cross section of the gene activity, or expression, that it provides, the potential for the early detection and diagnosis of cancer before morphogenesis has dramatically increased. While many statistical methods, such as cluster analysis, have been developed to tap into this enormous information source, a reliable method of early detection and diagnosis has yet to be developed. In this paper we propose using independent component analysis (ICA) as a first step in a process to identify diseased tissue solely based on its gene expression profile. In the ICA vernacular, a set of genes can be viewed as the sensors while certain biological processes, including the manifestation of a given disease, can be viewed as the signals. The goal then is to identify one or more 'demixed' signals, or signatures, that can be associated with the given disease. The demixing matrix can then be used to find the biological signals of an unknown sample, which might, in turn, be used for diagnosis when compared to the previously determined disease signatures. In this paper we explore the use of this technique on a previously studied melanoma dataset (Bittner, et. al., 2000).
机译:随着高通量DNA微阵列的出现和基因活性的大横截面,或表达,它提供的,在形态发生之前,癌症早期检测和诊断的可能性显着增加。虽然已经开发出许多统计方法,例如聚类分析以利用这种巨大的信息源,但尚未开发出可靠的早期检测和诊断方法。在本文中,我们将使用独立的分量分析(ICA)作为一种过程中仅基于其基因表达谱来鉴定患病组织的第一步。在ICA白天,可以将一组基因视为传感器,而某些生物过程,包括给定疾病的表现,可以被视为信号。然后,目标是识别可以与给定疾病相关联的一个或多个“解脱枯的”信号或签名。然后可以使用解析矩阵来找到未知样品的生物信号,其可能又用于与先前确定的疾病签名相比的诊断。在本文中,我们探讨了这种技术在先前研究的黑色素瘤数据集(Bittner等,2000)。

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