ArticleBMC bioinformatics2016
CMIP: a software package capable of reconstructing genome-wide regulatory networks using gene expression data.
Article in BMC bioinformatics, 2016. 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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Who cites it
8 citing papers in PubMed.
- Evolution of gene regulatory network of CPlant communications · 2023Article
- Parallel sequence tagging for concept recognition.BMC bioinformatics · 2022Article
- Genome-wide dynamic network analysis reveals the potential genes for MeJA-induced growth-to-defense transition.BMC plant biology · 2021Article
- Mechanistic Modeling of Gene Regulation and Metabolism Identifies Potential Targets for Hepatocellular Carcinoma.Frontiers in genetics · 2020Article
- Time of day and network reprogramming during drought induced CAM photosynthesis in Sedum album.PLoS genetics · 2019Article
- Parallel Algorithms for Inferring Gene Regulatory Networks: A Review.Current genomics · 2018Review
- Improving GRN re-construction by mining hidden regulatory signals.IET systems biology · 2017Article
- CytoCluster: A Cytoscape Plugin for Cluster Analysis and Visualization of Biological Networks.International journal of molecular sciences · 2017Article
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Authors and funding
7 authors.
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Abstract
backgroundA gene regulatory network (GRN) represents interactions of genes inside a cell or tissue, in which vertexes and edges stand for genes and their regulatory interactions respectively. Reconstruction of gene regulatory networks, in particular, genome-scale networks, is essential for comparative exploration of different species and mechanistic investigation of biological processes. Currently, most of network inference methods are computationally intensive, which are usually effective for small-scale tasks (e.g., networks with a few hundred genes), but are difficult to construct GRNs at genome-scale.
resultsHere, we present a software package for gene regulatory network reconstruction at a genomic level, in which gene interaction is measured by the conditional mutual information measurement using a parallel computing framework (so the package is named CMIP). The package is a greatly improved implementation of our previous PCA-CMI algorithm. In CMIP, we provide not only an automatic threshold determination method but also an effective parallel computing framework for network inference. Performance tests on benchmark datasets show that the accuracy of CMIP is comparable to most current network inference methods. Moreover, running tests on synthetic datasets demonstrate that CMIP can handle large datasets especially genome-wide datasets within an acceptable time period. In addition, successful application on a real genomic dataset confirms its practical applicability of the package.
conclusionsThis new software package provides a powerful tool for genomic network reconstruction to biological community. The software can be accessed at http://www.picb.ac.cn/CMIP/ .
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