scholarly journals HSCVFNT: Inference of Time-Delayed Gene Regulatory Network Based on Complex-Valued Flexible Neural Tree Model

2018 ◽  
Vol 19 (10) ◽  
pp. 3178 ◽  
Author(s):  
Bin Yang ◽  
Yuehui Chen ◽  
Wei Zhang ◽  
Jiaguo Lv ◽  
Wenzheng Bao ◽  
...  
Keyword(s):  
Time Series ◽  
Gene Regulatory Network ◽  
Regulatory Network ◽  
Target Gene ◽  
Repair System ◽  
Tree Model ◽  
Scoring Method ◽  
Maximum Information ◽  
Gene Regulatory ◽  
Complex Valued

Gene regulatory network (GRN) inference can understand the growth and development of animals and plants, and reveal the mystery of biology. Many computational approaches have been proposed to infer GRN. However, these inference approaches have hardly met the need of modeling, and the reducing redundancy methods based on individual information theory method have bad universality and stability. To overcome the limitations and shortcomings, this thesis proposes a novel algorithm, named HSCVFNT, to infer gene regulatory network with time-delayed regulations by utilizing a hybrid scoring method and complex-valued flexible neural network (CVFNT). The regulations of each target gene can be obtained by iteratively performing HSCVFNT. For each target gene, the HSCVFNT algorithm utilizes a novel scoring method based on time-delayed mutual information (TDMI), time-delayed maximum information coefficient (TDMIC) and time-delayed correlation coefficient (TDCC), to reduce the redundancy of regulatory relationships and obtain the candidate regulatory factor set. Then, the TDCC method is utilized to create time-delayed gene expression time-series matrix. Finally, a complex-valued flexible neural tree model is proposed to infer the time-delayed regulations of each target gene with the time-delayed time-series matrix. Three real time-series expression datasets from (Save Our Soul) SOS DNA repair system in E. coli and Saccharomyces cerevisiae are utilized to evaluate the performance of the HSCVFNT algorithm. As a result, HSCVFNT obtains outstanding F-scores of 0.923, 0.8 and 0.625 for SOS network and (In vivo Reverse-Engineering and Modeling Assessment) IRMA network inference, respectively, which are 5.5%, 14.3% and 72.2% higher than the best performance of other state-of-the-art GRN inference methods and time-delayed methods.

Deciphering the transcription factor-microRNA-target gene regulatory network associated with graphene oxide cytotoxicity

2018 ◽  
Vol 12 (9) ◽  
pp. 1014-1026 ◽  
Author(s):  
Masoumeh Farahani ◽  
Mostafa Rezaei–Tavirani ◽  
Hakimeh Zali ◽  
Afsaneh Arefi Oskouie ◽  
Meisam Omidi ◽  
...  
Keyword(s):  
Transcription Factor ◽  
Graphene Oxide ◽  
Gene Regulatory Network ◽  
Regulatory Network ◽  
Target Gene ◽  
Microrna Target ◽  
Gene Regulatory

Inferring Gene Regulatory Network Models from Time-Series Data Using Metaheuristics

2020 ◽  
Author(s):  
Jose Eduardo H. da Silva ◽  
Heder S. Betnardino ◽  
Helio J.C. Barbosa ◽  
Alex B. Vieira ◽  
Luciana C.D. Campos ◽  
...  
Keyword(s):  
Time Series ◽  
Gene Regulatory Network ◽  
Regulatory Network ◽  
Time Series Data ◽  
Network Models ◽  
Series Data ◽  
Gene Regulatory

scholarly journals Mining Featured Biomarkers Linked with Epithelial Ovarian Cancer Based on Bioinformatics

Diagnostics ◽  
2019 ◽  
Vol 9 (2) ◽  
pp. 39
Author(s):  
◽  
Chanabasayya Vastrad ◽  
◽  
Keyword(s):  
Gene Regulatory Network ◽  
Regulatory Network ◽  
Target Gene ◽  
Enrichment Analysis ◽  
Microrna Target ◽  
Pathway Enrichment ◽  
Protein Protein Interaction ◽  
Go Enrichment ◽  
Gene Regulatory ◽  
Go Enrichment Analysis

: Epithelial ovarian cancer (EOC) is the18th most common cancer worldwide and the 8th most common in women. The aim of this study was to diagnose the potential importance of, as well as novel genes linked with, EOC and to provide valid biological information for further research. The gene expression profiles of E-MTAB-3706 which contained four high-grade ovarian epithelial cancer samples, four normal fallopian tube samples and four normal ovarian epithelium samples were downloaded from the ArrayExpress database. Pathway enrichment and Gene Ontology (GO) enrichment analysis of differentially expressed genes (DEGs) were performed, and protein-protein interaction (PPI) network, microRNA-target gene regulatory network and TFs (transcription factors ) -target gene regulatory network for up- and down-regulated were analyzed using Cytoscape. In total, 552 DEGs were found, including 276 up-regulated and 276 down-regulated DEGs. Pathway enrichment analysis demonstrated that most DEGs were significantly enriched in chemical carcinogenesis, urea cycle, cell adhesion molecules and creatine biosynthesis. GO enrichment analysis showed that most DEGs were significantly enriched in translation, nucleosome, extracellular matrix organization and extracellular matrix. From protein-protein interaction network (PPI) analysis, modules, microRNA-target gene regulatory network and TFs-target gene regulatory network for up- and down-regulated, and the top hub genes such as E2F4, SRPK2, A2M, CDH1, MAP1LC3A, UCHL1, HLA-C (major histocompatibility complex, class I, C) , VAT1, ECM1 and SNRPN (small nuclear ribonucleoprotein polypeptide N) were associated in pathogenesis of EOC. The high expression levels of the hub genes such as CEBPD (CCAAT enhancer binding protein delta) and MID2 in stages 3 and 4 were validated in the TCGA (The Cancer Genome Atlas) database. CEBPD andMID2 were associated with the worst overall survival rates in EOC. In conclusion, the current study diagnosed DEGs between normal and EOC samples, which could improve our understanding of the molecular mechanisms in the progression of EOC. These new key biomarkers might be used as therapeutic targets for EOC.

scholarly journals A simple test to infer mode of selection in metagenomics time series of evolving asexual populations

2020 ◽  
Author(s):  
Rohan Maddamsetti ◽  
Nkrumah A. Grant
Keyword(s):  
Time Series ◽  
Positive Selection ◽  
Gene Regulatory Network ◽  
Regulatory Network ◽  
Fine Tuning ◽  
Simple Test ◽  
Regulatory Regions ◽  
E Coli ◽  
Gene Regulatory ◽  
Asexual Populations

ABSTRACTWe introduce a simple test to infer mode of selection (STIMS) in metagenomic time series of evolving asexual populations. STIMS compares the tempo of molecular evolution for a gene set of interest against a null distribution that is bootstrapped on random gene sets. We test STIMS on metagenomic data spanning 62,750 generations of Lenski’s long-term evolution experiment with E. coli (LTEE). Our method successfully recovers signals of purifying selection and positive selection on gold standard sets of genes. We then use STIMS to study the evolution of genetic modules in the LTEE. We find strong evidence of ongoing positive selection on key regulators of the E. coli gene regulatory network. Key regulatory genes show evidence of positive selection over the entire time series, even in some hypermutator populations. By contrast, we found no signal of selection on the genetic modules that show the strongest transcriptional responses to changes in growth conditions. In addition, the cis-regulatory regions of key regulators are evolving faster than the cis-regulatory regions of their downstream regulatory targets. These results indicate that one mechanistic cause for ongoing fitness gains in the LTEE is ongoing fine-tuning of the gene regulatory network.

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