TY - JOUR
T1 - TGCnA
T2 - temporal gene coexpression network analysis using a low-rank plus sparse framework
AU - Li, Jinyu
AU - Lai, Yutong
AU - Zhang, Chi
AU - Zhang, Qi
N1 - Funding Information:
This work has been supported by NSF ABI (Division of Biological Infrastructure) (Award# DBI-1564621), NSF EPSCoR (RII) Track II (Office of Integrative Activities) (Award# OIA-1736192) and NU Collaborative System Science Seed Grant to CZ and QZ. We thank the Holland Computing Center (HCC) at UNL for computation resources and technical supports. A previous version of this paper is available on bioRxiv [24].
Publisher Copyright:
© 2019, © 2019 Informa UK Limited, trading as Taylor & Francis Group.
PY - 2020/4/25
Y1 - 2020/4/25
N2 - Various gene network models with distinct physical nature have been widely used in biological studies. For temporal transcriptomic studies, the current dynamic models either ignore the temporal variation in the network structure or fail to scale up to a large number of genes due to severe computational bottlenecks and sample size limitation. Although the correlation-based gene networks are computationally affordable, they have limitations after being applied to gene expression time-course data. We proposed Temporal Gene Coexpression Network Analysis (TGCnA) framework for the transcriptomic time-course data. The mathematical nature of TGCnA is the joint modeling of multiple covariance matrices across time points using a ‘low-rank plus sparse’ framework, in which the network similarity across time points is explicitly modeled in the low-rank component. We demonstrated the advantage of TGCnA in covariance matrix estimation and gene module discovery using both simulation data and real transcriptomic data. The code is available at https://github.com/QiZhangStat/TGCnA.
AB - Various gene network models with distinct physical nature have been widely used in biological studies. For temporal transcriptomic studies, the current dynamic models either ignore the temporal variation in the network structure or fail to scale up to a large number of genes due to severe computational bottlenecks and sample size limitation. Although the correlation-based gene networks are computationally affordable, they have limitations after being applied to gene expression time-course data. We proposed Temporal Gene Coexpression Network Analysis (TGCnA) framework for the transcriptomic time-course data. The mathematical nature of TGCnA is the joint modeling of multiple covariance matrices across time points using a ‘low-rank plus sparse’ framework, in which the network similarity across time points is explicitly modeled in the low-rank component. We demonstrated the advantage of TGCnA in covariance matrix estimation and gene module discovery using both simulation data and real transcriptomic data. The code is available at https://github.com/QiZhangStat/TGCnA.
KW - Gene coexpression
KW - KEGG
KW - WGCNA
KW - covariance matrix estimation
KW - low-rank plus sparse
KW - transcriptomic time course
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U2 - 10.1080/02664763.2019.1667311
DO - 10.1080/02664763.2019.1667311
M3 - Article
C2 - 35706920
AN - SCOPUS:85073957267
SN - 0266-4763
VL - 47
SP - 1064
EP - 1083
JO - Journal of Applied Statistics
JF - Journal of Applied Statistics
IS - 6
ER -