Generating the logicome from microarray data

Charmi Panchal, V. Rogojin
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Abstract

The advances in complex statistics and machine learning methods lead to the development of powerful classifiers that can be used to recognize cellular states (such as gene expression profiles) that are associated to a number of gene-scale expressed diseases, for instance, cancer. However, the data-driven models built by means of learning from datasets in a number of cases represent “black boxes” that cannot be easily analyzed and understood. In this article, we suggest a method for building a data-driven logicome. I.e., the method for building a set of small boolean expressions as classifiers for disjoint groups of samples from a microarray dataset. We validate our method on the microarray dataset of head and neck/oral squamous cell carcinoma, where our boolean signature presented a set of gene activity/inactivity combinations that are characteristic for various cancer sub-types and normal samples. Our findings correlate well with the literature.
从微阵列数据生成逻辑组
复杂统计学和机器学习方法的进步导致了强大分类器的发展,这些分类器可用于识别与许多基因尺度表达疾病(例如癌症)相关的细胞状态(例如基因表达谱)。然而,在许多情况下,通过从数据集学习而建立的数据驱动模型代表了不容易分析和理解的“黑盒子”。在本文中,我们建议一种构建数据驱动逻辑集的方法。即,构建一组小布尔表达式作为微阵列数据集中不相交样本组的分类器的方法。我们在头颈部/口腔鳞状细胞癌的微阵列数据集上验证了我们的方法,其中我们的布尔签名呈现了一组基因活性/不活性组合,这些组合是各种癌症亚型和正常样本的特征。我们的发现与文献很吻合。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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