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Symbolic Data Analysis to Defy Low Signal-to-Noise Ratio in Microarray Data for Breast Cancer Prognosis

机译:符号数据分析可克服微阵列数据中低信噪比的乳腺癌预后

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摘要

>Microarray profiling has recently generated the hope to gain new insights into breast cancer biology and thereby improve the performance of current prognostic tools. However, it also poses several serious challenges to classical data analysis techniques related to the characteristics of resulting data, mainly high dimensionality and low signal-to-noise ratio. Despite the tremendous research work performed to handle the first challenge in the feature selection framework, very little attention has been directed to address the second one. We propose in this article to address both issues simultaneously based on symbolic data analysis capabilities in order to derive more accurate genetic marker–based prognostic models. In particular, interval data representation is employed to model various uncertainties in microarray measurements. A recent feature selection algorithm that handles symbolic interval data is used then to derive a genetic signature. The predictive value of the derived signature is then assessed by following a rigorous experimental setup and compared with existing prognostic approaches in terms of predictive performance and estimated survival probability. It is shown that the derived signature (GenSym) performs significantly better than other prognostic models, including the 70-gene signature, St. Gallen, and National Institutes of Health criteria.
机译:>最近,微阵列分析已成为希望获得对乳腺癌生物学的新见解,从而改善当前预后工具性能的希望。但是,它也对与所得数据的特征有关的经典数据分析技术提出了一些严峻的挑战,主要是高维数和低信噪比。尽管为解决功能选择框架中的第一个挑战而进行了大量的研究工作,但针对第二个挑战的关注却很少。我们在本文中建议基于符号数据分析功能同时解决这两个问题,以便得出更准确的基于遗传标记的预测模型。特别地,间隔数据表示被用来对微阵列测量中的各种不确定性建模。然后使用处理符号间隔数据的最新特征选择算法来导出遗传签名。然后,通过遵循严格的实验设置评估派生签名的预测价值,并在预测性能和估计的生存概率方面与现有的预后方法进行比较。结果表明,衍生签名(GenSym)的性能明显优于其他预后模型,包括70个基因的签名,St。Gallen和国立卫生研究院的标准

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