ArticleBMC systems biology2013
Disentangling function from topology to infer the network properties of disease genes.
Article in BMC systems biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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Who cites it
10 citing papers in PubMed, 18 citations in OpenAlex.
- Three topological features of regulatory networks control life-essential and specialized subsystems.Scientific reports · 2021Article
- Applications of molecular networks in biomedicine.Biology methods & protocols · 2019Review
- Arete - candidate gene prioritization using biological network topology with additional evidence types.BioData mining · 2017Article
- Predicting chemotherapeutic drug combinations through gene network profiling.Scientific reports · 2016Article
- Genome-Wide Detection and Analysis of Multifunctional Genes.PLoS computational biology · 2015Article
- Scale-space measures for graph topology link protein network architecture to function.Bioinformatics (Oxford, England) · 2014Article
- Interaction-based discovery of functionally important genes in cancers.Nucleic acids research · 2014Article
- Characterization of regulatory features of housekeeping and tissue-specific regulators within tissue regulatory networks.BMC systems biology · 2013Article
- Reconstruction of the experimentally supported human protein interactome: what can we learn?BMC systems biology · 2013Article
- Simple topological features reflect dynamics and modularity in protein interaction networks.PLoS computational biology · 2013Article
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Authors and funding
2 authors at 1 institution in 1 country.
Funding
Abstract
backgroundThe topological features of disease genes within interaction networks are the subject of intense study, as they shed light on common mechanisms of pathology and are useful for uncovering additional disease genes. Computational analyses typically try to uncover whether disease genes exhibit distinct network features, as compared to all genes.
resultsWe demonstrate that the functional composition of disease gene sets is an important confounding factor in these types of analyses. We consider five disease sets and show that while they indeed have distinct topological features, they are also enriched in functions that a priori exhibit distinct network properties. To address this, we develop a computational framework to assess the network properties of disease genes based on a sampling algorithm that generates control gene sets that are functionally similar to the disease set. Using our function-constrained sampling approach, we demonstrate that for most of the topological properties studied, disease genes are more similar to sets of genes with similar functional make-up than they are to randomly selected genes; this suggests that these observed differences in topological properties reflect not only the distinguishing network features of disease genes but also their functional composition. Nevertheless, we also highlight many cases where disease genes have distinct topological properties even when accounting for function.
conclusionsOur approach is an important first step in extracting the residual topological differences in disease genes when accounting for function, and leads to new insights into the network properties of disease genes.
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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.