Abstract

Gene regulatory network can intuitively reflect the interaction between genes, and an in-depth study of these relationships plays a significant role in the treatment and prevention of clinical diseases. Therefore, correct reconstruction of gene regulatory network has become the first critical step in the study of disease treatment and prevention at the genetic level. Among the methods for gene regulatory network reconstruction, the Bayesian network model has been widely concerned because of its advantages of expressing both the regulatory relationship and the degree of strength between genes. Nevertheless, the complexity of the Bayesian network model in structure learning is extremely high, making the efficiency of the reconstruction network is low and the scale is limited. Therefore, this paper proposed a dynamic Bayesian network modeling based on structure prediction (DBN-SP). The method combines the correlation model with the dynamic Bayesian network model. On the premise of making full use of the search strategy of dynamic Bayesian network model structure learning, the candidate parent node set is selected based on the structure prediction firstly. Based on this, some redundant information can be removed and the search space can be reduced in the DBN structure learning to improves the efficiency of the network reconstruction. After the network is reconstructed, structure optimization by using the conditional mutual information method can further remove redundant edges and make the network more accurate. The experimental results show that DBN-SP greatly improves the efficiency and scale of the gene regulatory network reconstruction, and the accuracy and other indexes are also improved. DBN-SP is freely accessible at https://github.com/quluxuan/DBN-SP.git .

Highlights

  • Gene is the material basis of heredity and the code to decipher all human life [1]–[3]

  • EXPERIMENTAL SETTINGS The experiment was mainly divided into two parts, that is, using the small-scale network to evaluate the performance of the Dynamic Bayesian Network (DBN)-SP method, and using the relatively large-scale network to evaluate the reconstruction scale of the network

  • We can see that the performance of DBN-SP was better than CNMIT [40] in True Positive Rate (TPR) which measured the number of True Positive (TP) edges and CNMIT [40] was better than DBN-SP in False Positive Rate (FPR) index which measured the number of False Positive (FP) edges

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Summary

Introduction

Gene is the material basis of heredity and the code to decipher all human life [1]–[3]. The differences in gene expression lead to many otherness in the natural characteristics of individuals [4], [5]. Common human diseases, such as neurodegenerative diseases, malignant tumors, and so on, are due to abnormal gene expression [6]–[8]. Finding out the upstream and downstream pathways of abnormal genes are of great significance in exploring the mechanism of the human body and the treatment of diseases. These are based on the reconstruction of the relatively correct gene regulatory network to study the relationships between genes. A more accurate and effective network reconstruction has become one of the problems in gene regulatory network research [10], [11]

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