INDEED: R package for network based differential expression analysis.

Zhenzhi Li, Yiming Zuo, Chaohui Xu, Rency S Varghese, Habtom W Ressom
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引用次数: 5

Abstract

With recent advancement of omics technologies, fueled by decreased cost and increased number of available datasets, computational methods for differential expression analysis are sought to identify disease-associated biomolecules. Conventional differential expression analysis methods (e.g. student's t-test, ANOVA) focus on assessing mean and variance of biomolecules in each biological group. On the other hand, network-based approaches take into account the interactions between biomolecules in choosing differentially expressed ones. These interactions are typically evaluated by correlation methods that tend to generate over-complicated networks due to many seemingly indirect associations. In this paper, we introduce a new R/Bioconductor package INDEED that allows users to construct a sparse network based on partial correlation, and to identify biomolecules that have significant changes both at individual expression and pairwise interaction levels. We applied INDEED for analysis of two omic datasets acquired in a cancer biomarker discovery study to help rank disease-associated biomolecules. We believe biomolecules selected by INDEED lead to improved sensitivity and specificity in detecting disease status compared to those selected by conventional statistical methods. Also, INDEED's framework is amenable to further expansion to integrate networks from multi-omic studies, thereby allowing selection of reliable disease-associated biomolecules or disease biomarkers.

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基于网络的差分表达式分析的R包。
随着组学技术的进步,成本的降低和可用数据集数量的增加,人们寻求用于差异表达分析的计算方法来识别疾病相关的生物分子。传统的差异表达分析方法(如学生t检验、方差分析)侧重于评估每个生物组中生物分子的均值和方差。另一方面,基于网络的方法在选择差异表达分子时考虑了生物分子之间的相互作用。这些相互作用通常通过相关方法进行评估,由于许多看似间接的关联,这些方法往往会产生过于复杂的网络。在本文中,我们引入了一个新的R/Bioconductor包INDEED,它允许用户构建基于偏相关的稀疏网络,并识别在个体表达和成对相互作用水平上都有显著变化的生物分子。我们应用了INDEED对癌症生物标志物发现研究中获得的两个组学数据集进行分析,以帮助对疾病相关生物分子进行排序。我们相信,与传统统计方法相比,通过INDEED选择的生物分子在检测疾病状态方面具有更高的敏感性和特异性。此外,INDEED的框架可以进一步扩展,以整合来自多组学研究的网络,从而允许选择可靠的疾病相关生物分子或疾病生物标志物。
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