Abstract
Previous researches focus on applying the Granger causality (GC) model to time-series DNA micro array data to infer gene regulatory networks. However, in biological datasets, the number of available time points is usually much smaller than the number of target genes. Therefore, people widely used a bivariate GC model, which might lead to a significant amount of false discoveries in the causality analysis. In this study, we proposed a new framework to resolve the problem by incorporating the prior biological knowledge. These prior knowledge helps us to use/build a gene association network and cluster the candidate gene set into smaller groups. Within each small group, the more precise multivariate GC model is applied to discover causalities. We validated this new framework to a yeast metabolic cycle dataset and initial analysis revealed the potentials of our approach in discovering meaningful regulatory networks.
Original language | English (US) |
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Title of host publication | Proceedings - IEEE 13th International Conference on Data Mining Workshops, ICDMW 2013 |
Publisher | IEEE Computer Society |
Pages | 124-130 |
Number of pages | 7 |
DOIs | |
State | Published - Jan 1 2013 |
Externally published | Yes |
Event | 2013 13th IEEE International Conference on Data Mining Workshops, ICDMW 2013 - Dallas, TX, United States Duration: Dec 7 2013 → Dec 10 2013 |
Other
Other | 2013 13th IEEE International Conference on Data Mining Workshops, ICDMW 2013 |
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Country/Territory | United States |
City | Dallas, TX |
Period | 12/7/13 → 12/10/13 |
All Science Journal Classification (ASJC) codes
- Software