TY - JOUR
T1 - A Multi-Laplacian Prior and Augmented Lagrangian Approach to the Exploratory Analysis of Time-Varying Gene and Transcriptional Regulatory Networks for Gene Microarray Data
AU - Zhang, Li
AU - Wu, Ho Chun
AU - Ho, Cheuk Hei
AU - Chan, Shing Chow
N1 - Publisher Copyright:
© 2004-2012 IEEE.
PY - 2019/11/1
Y1 - 2019/11/1
N2 - This paper proposes a novel multi-Laplacian prior (MLP) and augmented Lagrangian method (ALM) approach for gene interactions and putative transcription factors (TFs) identification from time-course gene microarray data. It employs a non-linear time-varying auto-regressive (N-TVAR) model and the Maximum-A-Posteriori-Probability method for incorporating the multi-Laplacian prior and the continuity constraint. The MLP allows connections to/from a gene to be better preserved for putative TF identification in non-stationarity gene regulatory network as compared with conventional L_1L1-based penalties. Moreover, the ALM allows the resultant non-smooth L_1L1-based penalties to be decoupled from the remaining smooth terms, so that the former and latter can be efficiently solved using a low-complexity proximity operator and smooth optimization technique, respectively. Synthetic and real time-course gene microarray datasets are tested to evaluate the performance of the proposed method. Experimental results show that the proposed method gives better accuracy and higher computational speed than our previous work using smoothed approximation. Moreover, its performance, without the use of ChIP-chip data, is found to be highly comparable with other state-of-the-art methods integrating both ChIP-chip and gene microarray data. It suggests that the proposed method may serve as a useful exploratory tool for putative TF identification with reduced experimental cost.
AB - This paper proposes a novel multi-Laplacian prior (MLP) and augmented Lagrangian method (ALM) approach for gene interactions and putative transcription factors (TFs) identification from time-course gene microarray data. It employs a non-linear time-varying auto-regressive (N-TVAR) model and the Maximum-A-Posteriori-Probability method for incorporating the multi-Laplacian prior and the continuity constraint. The MLP allows connections to/from a gene to be better preserved for putative TF identification in non-stationarity gene regulatory network as compared with conventional L_1L1-based penalties. Moreover, the ALM allows the resultant non-smooth L_1L1-based penalties to be decoupled from the remaining smooth terms, so that the former and latter can be efficiently solved using a low-complexity proximity operator and smooth optimization technique, respectively. Synthetic and real time-course gene microarray datasets are tested to evaluate the performance of the proposed method. Experimental results show that the proposed method gives better accuracy and higher computational speed than our previous work using smoothed approximation. Moreover, its performance, without the use of ChIP-chip data, is found to be highly comparable with other state-of-the-art methods integrating both ChIP-chip and gene microarray data. It suggests that the proposed method may serve as a useful exploratory tool for putative TF identification with reduced experimental cost.
KW - Gene regulatory networks
KW - augmented Lagrangian method
KW - gene microarray
KW - hub gene
KW - multi-Laplacian prior
KW - time-course data
KW - transcript factor
UR - http://www.scopus.com/inward/record.url?scp=85059046777&partnerID=8YFLogxK
U2 - 10.1109/TCBB.2018.2828810
DO - 10.1109/TCBB.2018.2828810
M3 - Article
C2 - 29993914
AN - SCOPUS:85059046777
SN - 1545-5963
VL - 16
SP - 1816
EP - 1829
JO - IEEE/ACM Transactions on Computational Biology and Bioinformatics
JF - IEEE/ACM Transactions on Computational Biology and Bioinformatics
IS - 6
M1 - 8344424
ER -