微分香农熵和微分变异系数:在寻找疾病相关基因中对差异表达的替代和增强。

Q4 Pharmacology, Toxicology and Pharmaceutics
Kai Wang, Charles A Phillips, Gary L Rogers, Fredrik Barrenas, Mikael Benson, Michael A Langston
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引用次数: 12

摘要

自微阵列技术出现以来,差异表达一直是分析病例对照转录组数据的标准工具。事实证明,它在描述疾病的分子机制方面是无价的。然而,一个基因在不同样本中的表达谱可能会受到干扰,但表达水平不变,而生物学效应仍然存在。本文描述并分析了差分香农熵和微分变异系数这两种鉴定感兴趣基因的方法。对16个人类疾病数据集的本体论分析表明,这些替代方法在识别仅通过差异表达无法发现的疾病相关基因方面是有效的。由于这两种替代技术基于不同的数学公式,它们往往会产生不同的基因列表。此外,每个人都可以精确定位被另一个人完全忽视的基因。因此,熵和变异的度量可以用来代替或更好地增强标准微分表达式计算。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Differential Shannon entropy and differential coefficient of variation: alternatives and augmentations to differential expression in the search for disease-related genes.

Differential Shannon entropy and differential coefficient of variation: alternatives and augmentations to differential expression in the search for disease-related genes.

Differential Shannon entropy and differential coefficient of variation: alternatives and augmentations to differential expression in the search for disease-related genes.

Differential Shannon entropy and differential coefficient of variation: alternatives and augmentations to differential expression in the search for disease-related genes.

Differential expression has been a standard tool for analysing case-control transcriptomic data since the advent of microarray technology. It has proved invaluable in characterising the molecular mechanisms of disease. Nevertheless, the expression profile of a gene across samples can be perturbed in ways that leave the expression level unaltered, while a biological effect is nonetheless present. This paper describes and analyses differential Shannon entropy and differential coefficient of variation, two alternate techniques for identifying genes of interest. Ontological analysis across 16 human disease datasets demonstrates that these alternatives are effective at identifying disease-related genes not found by mere differential expression alone. Because the two alternate techniques are based on somewhat different mathematical formulations, they tend to produce somewhat different gene lists. Moreover, each may pinpoint genes completely overlooked by the other. Thus, measures of entropy and variation can be used to replace or better yet augment standard differential expression computations.

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来源期刊
International Journal of Computational Biology and Drug Design
International Journal of Computational Biology and Drug Design Pharmacology, Toxicology and Pharmaceutics-Drug Discovery
CiteScore
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