A linear programming model for identifying non-redundant biomarkers based on gene expression profiles

X. Ren, Yong Wang, Luonan Chen, Xiang-Sun Zhang
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Abstract

With the development of high-throughput technologies, e.g. microarrays and the second generation sequencing technologies, gene expression profiles have been applied widely to characterize the functional states of various samples at different conditions. This is especially important for clinical biomarker identification that is vital to the understanding of the pathogenesis of a certain disease and the subsequent therapies. Because of the complexity of multi-gene disorders, a single biomarker or a set of separate biomarkers often fails to discriminate the samples correctly. Moreover, biomarker identification and class assignment of diseases are intrinsically linked while the current solutions to these two tasks are generally separated. Motivated by these issues, we give out a novel model based on linear programming in this study to simultaneously identify the most meaningful biomarkers and classify accurately the disease types for patients. Results on a few real data sets suggest the effectiveness and advantages of our method.
基于基因表达谱识别非冗余生物标志物的线性规划模型
随着微阵列技术和第二代测序技术等高通量技术的发展,基因表达谱被广泛应用于表征不同条件下各种样品的功能状态。这对于临床生物标志物的识别尤其重要,这对于理解某种疾病的发病机制和随后的治疗至关重要。由于多基因疾病的复杂性,单个生物标志物或一组单独的生物标志物往往不能正确区分样本。此外,生物标志物鉴定和疾病分类是内在联系的,而目前这两个任务的解决方案通常是分开的。在这些问题的激励下,本研究提出了一种基于线性规划的新模型,以同时识别最有意义的生物标志物并准确分类患者的疾病类型。在一些实际数据集上的结果表明了该方法的有效性和优越性。
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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