Abstract

BackgroundAlthough most of the current disease candidate gene identification and prioritization methods depend on functional annotations, the coverage of the gene functional annotations is a limiting factor. In the current study, we describe a candidate gene prioritization method that is entirely based on protein-protein interaction network (PPIN) analyses.ResultsFor the first time, extended versions of the PageRank and HITS algorithms, and the K-Step Markov method are applied to prioritize disease candidate genes in a training-test schema. Using a list of known disease-related genes from our earlier study as a training set ("seeds"), and the rest of the known genes as a test list, we perform large-scale cross validation to rank the candidate genes and also evaluate and compare the performance of our approach. Under appropriate settings – for example, a back probability of 0.3 for PageRank with Priors and HITS with Priors, and step size 6 for K-Step Markov method – the three methods achieved a comparable AUC value, suggesting a similar performance.ConclusionEven though network-based methods are generally not as effective as integrated functional annotation-based methods for disease candidate gene prioritization, in a one-to-one comparison, PPIN-based candidate gene prioritization performs better than all other gene features or annotations. Additionally, we demonstrate that methods used for studying both social and Web networks can be successfully used for disease candidate gene prioritization.

Highlights

  • Most of the current disease candidate gene identification and prioritization methods depend on functional annotations, the coverage of the gene functional annotations is a limiting factor

  • Most of the current disease candidate gene prioritization methods [1,2,3,4,5,6] rely on functional annotations

  • The remaining 265 genes are separated into 119 smaller components or sub networks of size two to five nodes or genes. Since majority of these smaller subnetworks contain only two genes, we reasoned that it might not be of interest to check the distribution of the disease genes among them

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Summary

Introduction

Most of the current disease candidate gene identification and prioritization methods depend on functional annotations, the coverage of the gene functional annotations is a limiting factor. We describe a candidate gene prioritization method that is entirely based on protein-protein interaction network (PPIN) analyses. Most of the current disease candidate gene prioritization methods [1,2,3,4,5,6] rely on functional annotations. The coverage of the gene functional annotations is a limiting factor. Analysis of protein-protein interaction networks (PPINs) is important for inferring the function of uncharacterized proteins. Protein-protein interactions refer to the association among the protein molecules and the study of these associations from the perspective of biochemistry, signal transduction and biomolecular networks.

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