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Identifying key genes in glaucoma based on a benchmarked dataset and the gene regulatory network
The current study aimed to identify key genes in glaucoma based on a benchmarked dataset and gene regulatory network (GRN). Local and global noise was added to the gene expression dataset to produce a benchmarked dataset. Differentially-expressed genes (DEGs) between patients with glaucoma and norma...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5647551/ https://www.ncbi.nlm.nih.gov/pubmed/29067091 http://dx.doi.org/10.3892/etm.2017.4931 |
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author | Chen, Xi Wang, Qiao-Ling Zhang, Meng-Hui |
author_facet | Chen, Xi Wang, Qiao-Ling Zhang, Meng-Hui |
author_sort | Chen, Xi |
collection | PubMed |
description | The current study aimed to identify key genes in glaucoma based on a benchmarked dataset and gene regulatory network (GRN). Local and global noise was added to the gene expression dataset to produce a benchmarked dataset. Differentially-expressed genes (DEGs) between patients with glaucoma and normal controls were identified utilizing the Linear Models for Microarray Data (Limma) package based on benchmarked dataset. A total of 5 GRN inference methods, including Zscore, GeneNet, context likelihood of relatedness (CLR) algorithm, Partial Correlation coefficient with Information Theory (PCIT) and GEne Network Inference with Ensemble of Trees (Genie3) were evaluated using receiver operating characteristic (ROC) and precision and recall (PR) curves. The interference method with the best performance was selected to construct the GRN. Subsequently, topological centrality (degree, closeness and betweenness) was conducted to identify key genes in the GRN of glaucoma. Finally, the key genes were validated by performing reverse transcription-quantitative polymerase chain reaction (RT-qPCR). A total of 176 DEGs were detected from the benchmarked dataset. The ROC and PR curves of the 5 methods were analyzed and it was determined that Genie3 had a clear advantage over the other methods; thus, Genie3 was used to construct the GRN. Following topological centrality analysis, 14 key genes for glaucoma were identified, including IL6, EPHA2 and GSTT1 and 5 of these 14 key genes were validated by RT-qPCR. Therefore, the current study identified 14 key genes in glaucoma, which may be potential biomarkers to use in the diagnosis of glaucoma and aid in identifying the molecular mechanism of this disease. |
format | Online Article Text |
id | pubmed-5647551 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-56475512017-10-24 Identifying key genes in glaucoma based on a benchmarked dataset and the gene regulatory network Chen, Xi Wang, Qiao-Ling Zhang, Meng-Hui Exp Ther Med Articles The current study aimed to identify key genes in glaucoma based on a benchmarked dataset and gene regulatory network (GRN). Local and global noise was added to the gene expression dataset to produce a benchmarked dataset. Differentially-expressed genes (DEGs) between patients with glaucoma and normal controls were identified utilizing the Linear Models for Microarray Data (Limma) package based on benchmarked dataset. A total of 5 GRN inference methods, including Zscore, GeneNet, context likelihood of relatedness (CLR) algorithm, Partial Correlation coefficient with Information Theory (PCIT) and GEne Network Inference with Ensemble of Trees (Genie3) were evaluated using receiver operating characteristic (ROC) and precision and recall (PR) curves. The interference method with the best performance was selected to construct the GRN. Subsequently, topological centrality (degree, closeness and betweenness) was conducted to identify key genes in the GRN of glaucoma. Finally, the key genes were validated by performing reverse transcription-quantitative polymerase chain reaction (RT-qPCR). A total of 176 DEGs were detected from the benchmarked dataset. The ROC and PR curves of the 5 methods were analyzed and it was determined that Genie3 had a clear advantage over the other methods; thus, Genie3 was used to construct the GRN. Following topological centrality analysis, 14 key genes for glaucoma were identified, including IL6, EPHA2 and GSTT1 and 5 of these 14 key genes were validated by RT-qPCR. Therefore, the current study identified 14 key genes in glaucoma, which may be potential biomarkers to use in the diagnosis of glaucoma and aid in identifying the molecular mechanism of this disease. D.A. Spandidos 2017-10 2017-08-16 /pmc/articles/PMC5647551/ /pubmed/29067091 http://dx.doi.org/10.3892/etm.2017.4931 Text en Copyright: © Chen et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Chen, Xi Wang, Qiao-Ling Zhang, Meng-Hui Identifying key genes in glaucoma based on a benchmarked dataset and the gene regulatory network |
title | Identifying key genes in glaucoma based on a benchmarked dataset and the gene regulatory network |
title_full | Identifying key genes in glaucoma based on a benchmarked dataset and the gene regulatory network |
title_fullStr | Identifying key genes in glaucoma based on a benchmarked dataset and the gene regulatory network |
title_full_unstemmed | Identifying key genes in glaucoma based on a benchmarked dataset and the gene regulatory network |
title_short | Identifying key genes in glaucoma based on a benchmarked dataset and the gene regulatory network |
title_sort | identifying key genes in glaucoma based on a benchmarked dataset and the gene regulatory network |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5647551/ https://www.ncbi.nlm.nih.gov/pubmed/29067091 http://dx.doi.org/10.3892/etm.2017.4931 |
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