ArticlePloS one2013
Identifying gene set association enrichment using the coefficient of intrinsic dependence.
Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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Who cites it
4 citing papers in PubMed.
- Redundancy-aware unsupervised ranking based on game theory: Ranking pathways in collections of gene sets.PloS one · 2023Article
- Identification of DYNLT1 associated with proliferation, relapse, and metastasis in breast cancer.Frontiers in medicine · 2023Article
- Construction of gene causal regulatory networks using microarray data with the coefficient of intrinsic dependence.Botanical studies · 2019Article
- Microarray meta-analysis to explore abiotic stress-specific gene expression patterns in Arabidopsis.Botanical studies · 2017Article
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Authors and funding
2 authors.
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Abstract
Gene set testing problem has become the focus of microarray data analysis. A gene set is a group of genes that are defined by a priori biological knowledge. Several statistical methods have been proposed to determine whether functional gene sets express differentially (enrichment and/or deletion) in variations of phenotypes. However, little attention has been given to analyzing the dependence structure among gene sets. In this study, we have proposed a novel statistical method of gene set association analysis to identify significantly associated gene sets using the coefficient of intrinsic dependence. The simulation studies show that the proposed method outperforms the conventional methods to detect general forms of association in terms of control of type I error and power. The correlation of intrinsic dependence has been applied to a breast cancer microarray dataset to quantify the un-supervised relationship between two sets of genes in the tumor and non-tumor samples. It was observed that the existence of gene-set association differed across various clinical cohorts. In addition, a supervised learning was employed to illustrate how gene sets, in signaling transduction pathways or subnetworks regulated by a set of transcription factors, can be discovered using microarray data. In conclusion, the coefficient of intrinsic dependence provides a powerful tool for detecting general types of association. Hence, it can be useful to associate gene sets using microarray expression data. Through connecting relevant gene sets, our approach has the potential to reveal underlying associations by drawing a statistically relevant network in a given population, and it can also be used to complement the conventional gene set analysis.
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