ArticleBioinformatics (Oxford, England)2012
Robust identification of transcriptional regulatory networks using a Gibbs sampler on outlier sum statistic.
Article in Bioinformatics (Oxford, England), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed, 9 citations in OpenAlex.
- Identifying intracellular signaling modules and exploring pathways associated with breast cancer recurrence.Scientific reports · 2021Article
- Breaking the paradigm: Dr Insight empowers signature-free, enhanced drug repurposing.Bioinformatics (Oxford, England) · 2019Article
- CRNET: an efficient sampling approach to infer functional regulatory networks by integrating large-scale ChIP-seq and time-course RNA-seq data.Bioinformatics (Oxford, England) · 2018Article
- mAPC-GibbsOS: an integrated approach for robust identification of gene regulatory networks.BMC systems biology · 2013Article
- Antiestrogen Resistance and the Application of Systems Biology.Drug discovery today. Disease mechanisms · 2012Article
Corrections and comments
- Erratum issued
Authors and funding
6 authors at 2 institutions in 1 country.
Funding
Abstract
motivationIdentification of transcriptional regulatory networks (TRNs) is of significant importance in computational biology for cancer research, providing a critical building block to unravel disease pathways. However, existing methods for TRN identification suffer from the inclusion of excessive 'noise' in microarray data and false-positives in binding data, especially when applied to human tumor-derived cell line studies. More robust methods that can counteract the imperfection of data sources are therefore needed for reliable identification of TRNs in this context.
resultsIn this article, we propose to establish a link between the quality of one target gene to represent its regulator and the uncertainty of its expression to represent other target genes. Specifically, an outlier sum statistic was used to measure the aggregated evidence for regulation events between target genes and their corresponding transcription factors. A Gibbs sampling method was then developed to estimate the marginal distribution of the outlier sum statistic, hence, to uncover underlying regulatory relationships. To evaluate the effectiveness of our proposed method, we compared its performance with that of an existing sampling-based method using both simulation data and yeast cell cycle data. The experimental results show that our method consistently outperforms the competing method in different settings of signal-to-noise ratio and network topology, indicating its robustness for biological applications. Finally, we applied our method to breast cancer cell line data and demonstrated its ability to extract biologically meaningful regulatory modules related to estrogen signaling and action in breast cancer. AVAILABILITY AND IMPLEMENTATION: The Gibbs sampler MATLAB package is freely available at http://www.cbil.ece.vt.edu/software.htm. CONTACT: xuan@vt.edu SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.