PPIGCF: A Protein–Protein Interaction-Based Gene Correlation Filter for Optimal Gene Selection

Author:

Pati Soumen Kumar1,Gupta Manan Kumar1,Banerjee Ayan2ORCID,Mallik Saurav345,Zhao Zhongming36ORCID

Affiliation:

1. Department of Bioinformatics, Maulana Abul Kalam Azad University of Technology, Haringhata 741249, West Bengal, India

2. Department of Computer Science and Engineering, Jalpaiguri Govt. Engineering College, Jalpaiguri 735102, West Bengal, India

3. Center for Precision Health, School of Biomedical Informatics, The University of Texas Health Science Center at Houston, Houston, TX 77030, USA

4. Department of Environmental Health, Harvard T H Chan School of Public Health, Boston, MA 02115, USA

5. Department of Pharmacology & Toxicology, University of Arizona, Tucson, AZ 85721, USA

6. Human Genetics Center, School of Public Health, The University of Texas Health Science Center at Houston, Houston, TX 77030, USA

Abstract

Biological data at the omics level are highly complex, requiring powerful computational approaches to identifying significant intrinsic characteristics to further search for informative markers involved in the studied phenotype. In this paper, we propose a novel dimension reduction technique, protein–protein interaction-based gene correlation filtration (PPIGCF), which builds on gene ontology (GO) and protein–protein interaction (PPI) structures to analyze microarray gene expression data. PPIGCF first extracts the gene symbols with their expression from the experimental dataset, and then, classifies them based on GO biological process (BP) and cellular component (CC) annotations. Every classification group inherits all the information on its CCs, corresponding to the BPs, to establish a PPI network. Then, the gene correlation filter (regarding gene rank and the proposed correlation coefficient) is computed on every network and eradicates a few weakly correlated genes connected with their corresponding networks. PPIGCF finds the information content (IC) of the other genes related to the PPI network and takes only the genes with the highest IC values. The satisfactory results of PPIGCF are used to prioritize significant genes. We performed a comparison with current methods to demonstrate our technique’s efficiency. From the experiment, it can be concluded that PPIGCF needs fewer genes to reach reasonable accuracy (~99%) for cancer classification. This paper reduces the computational complexity and enhances the time complexity of biomarker discovery from datasets.

Funder

Cancer Prevention and Research Institute of Texas

Publisher

MDPI AG

Subject

Genetics (clinical),Genetics

Reference73 articles.

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3. An Integrative Framework for Protein Interaction Network and Methylation Data to Discover Epigenetic Modules;Ma;IEEE/ACM Trans. Comput. Biol. Bioinf.,2018

4. Banerjee, A., Pati, S.K., and Gupta, M.K. (2020). Computational Intelligence in Pattern Recognition, Springer.

5. Deciphering Brain Complexity Using Single-Cell Sequencing;Mu;Genom. Proteom. Bioinform.,2019

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