Affiliations 

  • 1 Department of Software Engineering, College of IT, University of Tenaga Nasional, Jalan IKRAM-UNITEN, 43000 Kajang, Malaysia. Electronic address: faridahh@uniten.edu.my
  • 2 Centre of Artificial Intelligence, Faculty of Information Sciences & Technology, Universiti Kebangsaan Malaysia, 43650 UKM Bangi, Malaysia. Electronic address: shereena.arif@ukm.edu.my
  • 3 Centre of Artificial Intelligence, Faculty of Information Sciences & Technology, Universiti Kebangsaan Malaysia, 43650 UKM Bangi, Malaysia. Electronic address: suhaila.zainudin@ukm.edu.my
  • 4 School of Biosciences & Biotechnology, Faculty of Science & Technology, Universiti Kebangsaan Malaysia, 43600 Bangi, Selangor, Malaysia. Electronic address: firdaus@mfrlab.org
Comput Biol Chem, 2015 Dec;59 Pt B:3-14.
PMID: 26278974 DOI: 10.1016/j.compbiolchem.2015.04.012

Abstract

A gene regulatory network (GRN) is a large and complex network consisting of interacting elements that, over time, affect each other's state. The dynamics of complex gene regulatory processes are difficult to understand using intuitive approaches alone. To overcome this problem, we propose an algorithm for inferring the regulatory interactions from knock-out data using a Gaussian model combines with Pearson Correlation Coefficient (PCC). There are several problems relating to GRN construction that have been outlined in this paper. We demonstrated the ability of our proposed method to (1) predict the presence of regulatory interactions between genes, (2) their directionality and (3) their states (activation or suppression). The algorithm was applied to network sizes of 10 and 50 genes from DREAM3 datasets and network sizes of 10 from DREAM4 datasets. The predicted networks were evaluated based on AUROC and AUPR. We discovered that high false positive values were generated by our GRN prediction methods because the indirect regulations have been wrongly predicted as true relationships. We achieved satisfactory results as the majority of sub-networks achieved AUROC values above 0.5.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.