Evidence map›Paper›PMID 22672776›Full record

ArticleBMC systems biology2012

Centrality-based pathway enrichment: a systematic approach for finding significant pathways dominated by key genes.

Zuguang Gu, Jialin Liu, Kunming Cao, Junfeng Zhang, Jin Wang

Abstract read
In one paragraph

Article in BMC systems biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

47 citing papers in PubMed.

  1. Article
  2. Distribution of centrality measures on undirected random networks via the cavity method.Proceedings of the National Academy of Sciences of the United States of America · 2024
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  7. Review
  8. Pathway expression analysis.Scientific reports · 2022
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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Zuguang GuThe State Key Laboratory of Pharmaceutical Biotechnology and Jiangsu Engineering Research Center for MicroRNA Biology and Biotechnology, School of Life Science, Nanjing University, Nanjing, 210093, China.
Jialin Liu
Kunming Cao
Junfeng Zhang
Jin Wang

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBiological pathways are important for understanding biological mechanisms. Thus, finding important pathways that underlie biological problems helps researchers to focus on the most relevant sets of genes. Pathways resemble networks with complicated structures, but most of the existing pathway enrichment tools ignore topological information embedded within pathways, which limits their applicability.

resultsA systematic and extensible pathway enrichment method in which nodes are weighted by network centrality was proposed. We demonstrate how choice of pathway structure and centrality measurement, as well as the presence of key genes, affects pathway significance. We emphasize two improvements of our method over current methods. First, allowing for the diversity of genes' characters and the difficulty of covering gene importance from all aspects, we set centrality as an optional parameter in the model. Second, nodes rather than genes form the basic unit of pathways, such that one node can be composed of several genes and one gene may reside in different nodes. By comparing our methodology to the original enrichment method using both simulation data and real-world data, we demonstrate the efficacy of our method in finding new pathways from biological perspective.

conclusionsOur method can benefit the systematic analysis of biological pathways and help to extract more meaningful information from gene expression data. The algorithm has been implemented as an R package CePa, and also a web-based version of CePa is provided.

Indexed as

AlgorithmsComputational BiologyComputer GraphicsGene Regulatory Networks

Identifiers

PMID22672776
PMCPMC3443660

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.