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- Publisher Website: 10.1109/TCBB.2018.2828810
- Scopus: eid_2-s2.0-85059046777
- PMID: 29993914
- WOS: WOS:000507924300005
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Article: A Multi-Laplacian Prior and Augmented Lagrangian Approach to the Exploratory Analysis of Time-Varying Gene and Transcriptional Regulatory Networks for Gene Microarray Data
Title | A Multi-Laplacian Prior and Augmented Lagrangian Approach to the Exploratory Analysis of Time-Varying Gene and Transcriptional Regulatory Networks for Gene Microarray Data |
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Authors | |
Keywords | Gene regulatory networks gene microarray hub gene time-course data transcript factor |
Issue Date | 2019 |
Publisher | IEEE. |
Citation | IEEE/ACM Transactions on Computational Biology and Bioinformatics, 2019, v. 16 n. 6, p. 1816-1829 How to Cite? |
Abstract | 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 1 -based penalties. Moreover, the ALM allows the resultant non-smooth L 1 -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. |
Persistent Identifier | http://hdl.handle.net/10722/293812 |
ISSN | 2023 Impact Factor: 3.6 2023 SCImago Journal Rankings: 0.794 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Zhang, L | - |
dc.contributor.author | Wu, HC | - |
dc.contributor.author | HO, CH | - |
dc.contributor.author | Chan, SC | - |
dc.date.accessioned | 2020-11-23T08:22:08Z | - |
dc.date.available | 2020-11-23T08:22:08Z | - |
dc.date.issued | 2019 | - |
dc.identifier.citation | IEEE/ACM Transactions on Computational Biology and Bioinformatics, 2019, v. 16 n. 6, p. 1816-1829 | - |
dc.identifier.issn | 1545-5963 | - |
dc.identifier.uri | http://hdl.handle.net/10722/293812 | - |
dc.description.abstract | 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 1 -based penalties. Moreover, the ALM allows the resultant non-smooth L 1 -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. | - |
dc.language | eng | - |
dc.publisher | IEEE. | - |
dc.relation.ispartof | IEEE/ACM Transactions on Computational Biology and Bioinformatics | - |
dc.rights | IEEE/ACM Transactions on Computational Biology and Bioinformatics. Copyright © IEEE. | - |
dc.rights | ©20xx IEEE. Personal use of this material is permitted. Permission from IEEE must be obtained for all other uses, in any current or future media, including reprinting/republishing this material for advertising or promotional purposes, creating new collective works, for resale or redistribution to servers or lists, or reuse of any copyrighted component of this work in other works. | - |
dc.subject | Gene regulatory networks | - |
dc.subject | gene microarray | - |
dc.subject | hub gene | - |
dc.subject | time-course data | - |
dc.subject | transcript factor | - |
dc.title | A Multi-Laplacian Prior and Augmented Lagrangian Approach to the Exploratory Analysis of Time-Varying Gene and Transcriptional Regulatory Networks for Gene Microarray Data | - |
dc.type | Article | - |
dc.identifier.email | Wu, HC: hcwueee@hku.hk | - |
dc.identifier.email | Chan, SC: scchan@eee.hku.hk | - |
dc.identifier.authority | Chan, SC=rp00094 | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1109/TCBB.2018.2828810 | - |
dc.identifier.pmid | 29993914 | - |
dc.identifier.scopus | eid_2-s2.0-85059046777 | - |
dc.identifier.hkuros | 319242 | - |
dc.identifier.volume | 16 | - |
dc.identifier.issue | 6 | - |
dc.identifier.spage | 1816 | - |
dc.identifier.epage | 1829 | - |
dc.identifier.isi | WOS:000507924300005 | - |
dc.publisher.place | United States | - |
dc.identifier.issnl | 1545-5963 | - |