TY - GEN
T1 - Dynamic gene and transcriptional regulatory networks inferring with multi-Laplacian prior from time-course gene microarray data
AU - Zhang, L.
AU - Wu, H. C.
AU - Chan, S. C.
AU - Wang, C.
N1 - Publisher Copyright:
© 2017 IEEE.
PY - 2017/11/3
Y1 - 2017/11/3
N2 - This paper presents a dynamic gene and transcriptional regulatory network inferring method by using the time-varying autoregressive (TVAR) model. It employs the Li-based regularization terms with spatial sparsity, temporal continuity and proposed multi-Laplacian prior (MLP) for key transcriptional factors (TFs) and their interactions identification. The MLP regularization allows the connections of a gene to be better preserved as a group so that putative TFs can be identified in dynamic gene network. Furthermore, an ADMM-based method is proposed to solve the problem by using the augmented Lagrangian multiplier technique. The simulation using DREAM 4 datasets shows the proposed method performs better than other well-established algorithms for gene network inferring. This enables us to apply the proposed method to a yeast cell cycle microarray datasets containing 215 genes and 17 timepoints more effectively. We are able to identify key genes and gene interactions align well with the natural of yeast cell cycle and related literatures. These suggest that the proposed method can serve as a useful exploratory tool for putative TFs and dynamic gene/TFs networks identification using microarray data.
AB - This paper presents a dynamic gene and transcriptional regulatory network inferring method by using the time-varying autoregressive (TVAR) model. It employs the Li-based regularization terms with spatial sparsity, temporal continuity and proposed multi-Laplacian prior (MLP) for key transcriptional factors (TFs) and their interactions identification. The MLP regularization allows the connections of a gene to be better preserved as a group so that putative TFs can be identified in dynamic gene network. Furthermore, an ADMM-based method is proposed to solve the problem by using the augmented Lagrangian multiplier technique. The simulation using DREAM 4 datasets shows the proposed method performs better than other well-established algorithms for gene network inferring. This enables us to apply the proposed method to a yeast cell cycle microarray datasets containing 215 genes and 17 timepoints more effectively. We are able to identify key genes and gene interactions align well with the natural of yeast cell cycle and related literatures. These suggest that the proposed method can serve as a useful exploratory tool for putative TFs and dynamic gene/TFs networks identification using microarray data.
UR - https://www.scopus.com/pages/publications/85040336174
U2 - 10.1109/ICDSP.2017.8096114
DO - 10.1109/ICDSP.2017.8096114
M3 - Conference contribution
AN - SCOPUS:85040336174
T3 - International Conference on Digital Signal Processing, DSP
BT - 2017 22nd International Conference on Digital Signal Processing, DSP 2017
T2 - 22nd International Conference on Digital Signal Processing, DSP 2017
Y2 - 23 August 2017 through 25 August 2017
ER -