Abstract

BackgroundThere are different and complicated associations between genes and diseases. Finding the causal associations between genes and specific diseases is still challenging. In this work we present a method to predict novel associations of genes and pathways with inflammatory bowel disease (IBD) by integrating information of differential gene expression, protein-protein interaction and known disease genes related to IBD.ResultsWe downloaded IBD gene expression data from NCBI’s Gene Expression Omnibus, performed statistical analysis to determine differentially expressed genes, collected known IBD genes from DisGeNet database, which were used to construct a IBD related PPI network with HIPPIE database. We adapted our graph-based clustering algorithm DPClusO to cluster the disease PPI network. We evaluated the statistical significance of the identified clusters in the context of determining the richness of IBD genes using Fisher’s exact test and predicted novel genes related to IBD. We showed 93.8% of our predictions are correct in the context of other databases and published literatures related to IBD.ConclusionsFinding disease-causing genes is necessary for developing drugs with synergistic effect targeting many genes simultaneously. Here we present an approach to identify novel disease genes and pathways and discuss our approach in the context of IBD. The approach can be generalized to find disease-associated genes for other diseases.

Highlights

  • There are different and complicated associations between genes and diseases

  • The Genome-wide association studies (GWAS) performed to date together with a meta-analyasis of several GWAS have identified a total of 163 inflammatory bowel disease (IBD) loci [1]

  • Out of 299 diseases only 20% of the respective known disease gene from some type of modules [24]. To compensate for such gaps to a certain extent, In the present work we focus on finding novel IBD associated genes and pathways by integrating IBD gene expression, Protein-protein interaction (PPI), and known IBD genes by adapting the DPClusO network clustering algorithm we published previously

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Summary

Introduction

There are different and complicated associations between genes and diseases. Finding the causal associations between genes and specific diseases is still challenging. There are two major subtypes of IBD: ulcerative colitis (UC) and Crohn’s disease (CD). Both types usually involve severe diarrhea, pain, fatigue and weight loss. The GWAS performed to date together with a meta-analyasis of several GWAS have identified a total of 163 IBD loci [1]. These studies mainly focused on the common genetic variants (single nucleotide polymorphisms (SNPs)).

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