Abstract
The problem of uncovering transcriptional regulation by transcription factors (TFs) based on microarray data is considered. A novel Bayesian sparse correlated rectified factor model (BSCRFM) is proposed that models the unknown TF protein level activity, the correlated regulations between TFs, and the sparse nature of TF regulated genes. The model admits prior knowledge from existing database regarding TF regulated target genes based on a sparse prior and through a developed Gibbs sampling algorithm, a context-specific transcriptional regulatory network specific to the experimental condition of the microarray data can be obtained. The proposed model and the Gibbs sampling algorithm were evaluated on the simulated systems and results demonstrated the validity and effectiveness of the proposed approach. The proposed model was then applied to the Breast cancer microarray data of patients with Estrogen Receptor positive ER+ status and Estrogen Receptor negative ER- status, respectively.
| Original language | English |
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| Title of host publication | ICSP2010 - 2010 IEEE 10th International Conference on Signal Processing, Proceedings |
| Pages | 1785-1788 |
| Number of pages | 4 |
| DOIs | |
| Publication status | Published - 2010 |
| Externally published | Yes |
| Event | 2010 IEEE 10th International Conference on Signal Processing, ICSP2010 - Beijing, China Duration: 24 Oct 2010 → 28 Oct 2010 |
Publication series
| Name | International Conference on Signal Processing Proceedings, ICSP |
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Conference
| Conference | 2010 IEEE 10th International Conference on Signal Processing, ICSP2010 |
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| Country/Territory | China |
| City | Beijing |
| Period | 24/10/10 → 28/10/10 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Bayesian sparse factor model
- Component
- Correlated non-negative factor
- Dirichlet process mixture (DPM)
- Gibbs sampling
- Rectified Gaussian mixture
- Transcriptional regulatory network
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