Highly sensitive inference of time-delayed gene regulations by network deconvolution — ASN Events

Highly sensitive inference of time-delayed gene regulations by network deconvolution (#81)

Haifen Chen 1 , Piyushkumar A. Mundra 2 , Li Na Zhao 1 , Feng Lin 1 , Jie Zheng 1 3
  1. Nanyang Technological University, Singapore
  2. Metabolomics Laboratory, Baker IDI Heart and Diabetes Institute, Melbourne, Australia
  3. Genome Institute of Singapore, Singapore

Background: Gene regulatory network (GRN) is a fundamental topic in systems biology. The dynamics of GRN can shed light on the cellular processes, which facilitates our understanding the mechanisms of disease when the processes are dysregulated. Accurate reconstruction of GRN could also provide guidelines for experimental biologists. Therefore, inferring gene regulatory network from high-throughput gene expression data is a central problem in systems biology. However, due to the inherent complexity of gene regulation, noise in measuring the data and short time-series data, it is very challenging to reconstruct accurate GRNs. On the other hand, a better understanding into gene regulation could help to improve the performance of GRN inference. Time delay is one of the most important characteristics of gene regulation. By incorporating the information of time delays, we can achieve more accurate inference of GRN.

Results: In this paper, we propose a method to infer time-delayed gene regulations based on cross-correlation and network deconvolution (ND). First, we employ cross-correlation to obtain the probable time delays for the interactions between each target gene and its potential regulators. Then based on the inferred delays, the technique of network deconvolution (ND) is applied to identify direct interactions between the target gene and its regulators. Experiments on real-life gene expression datasets show that our method achieves overall better performance than existing methods for inferring time-delayed GRNs.

Conclusion: By taking into account the time delays among gene interactions, our method is able to infer GRN more accurately. The effectiveness of our method has been shown by the experiments on three real-life gene expression datasets of yeast. Compared with other existing methods which were designed for learning time-delayed GRN, our method has significantly higher sensitivity without much reduction of specificity.