ArticleBMC systems biology2014
A group LASSO-based method for robustly inferring gene regulatory networks from multiple time-course datasets.
Article in BMC systems biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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8 citing papers in PubMed, 48 citations in OpenAlex.
- A Noise-Tolerating Gene Association Network Uncovering an Oncogenic Regulatory Motif in Lymphoma Transcriptomics.Life (Basel, Switzerland) · 2023Article
- Using single cell atlas data to reconstruct regulatory networks.Nucleic acids research · 2023Article
- Prediction of condition-specific regulatory genes using machine learning.Nucleic acids research · 2020Article
- fastBMA: scalable network inference and transitive reduction.GigaScience · 2017Article
- Adaptive modelling of gene regulatory network using Bayesian information criterion-guided sparse regression approach.IET systems biology · 2016Article
- GUIdock: Using Docker Containers with a Common Graphics User Interface to Address the Reproducibility of Research.PloS one · 2016Article
- CyNetworkBMA: a Cytoscape app for inferring gene regulatory networks.Source code for biology and medicine · 2015Article
- Computational Modeling of Gene-Specific Transcriptional Repression, Activation and Chromatin Interactions in Leukemogenesis by LASSO-Regularized Logistic Regression.IEEE/ACM transactions on computational biology and bioinformaticsArticle
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Authors and funding
3 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundAs an abstract mapping of the gene regulations in the cell, gene regulatory network is important to both biological research study and practical applications. The reverse engineering of gene regulatory networks from microarray gene expression data is a challenging research problem in systems biology. With the development of biological technologies, multiple time-course gene expression datasets might be collected for a specific gene network under different circumstances. The inference of a gene regulatory network can be improved by integrating these multiple datasets. It is also known that gene expression data may be contaminated with large errors or outliers, which may affect the inference results.
resultsA novel method, Huber group LASSO, is proposed to infer the same underlying network topology from multiple time-course gene expression datasets as well as to take the robustness to large error or outliers into account. To solve the optimization problem involved in the proposed method, an efficient algorithm which combines the ideas of auxiliary function minimization and block descent is developed. A stability selection method is adapted to our method to find a network topology consisting of edges with scores. The proposed method is applied to both simulation datasets and real experimental datasets. It shows that Huber group LASSO outperforms the group LASSO in terms of both areas under receiver operating characteristic curves and areas under the precision-recall curves.
conclusionsThe convergence analysis of the algorithm theoretically shows that the sequence generated from the algorithm converges to the optimal solution of the problem. The simulation and real data examples demonstrate the effectiveness of the Huber group LASSO in integrating multiple time-course gene expression datasets and improving the resistance to large errors or outliers.
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