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Identification of dysregulated modules based on network entropy in type 1 diabetes
Type 1 diabetes is a prevalent autoimmune disease of which the underlying mechanisms remain to be elucidated. The aim of the study was to identify dysregulated modules of type 1 diabetes. After microarray data were preprocessed, 20,545 genes were obtained. By integrating gene expression data and pro...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5841047/ https://www.ncbi.nlm.nih.gov/pubmed/29545837 http://dx.doi.org/10.3892/etm.2018.5803 |
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author | Zheng, Yan Liu, Liwei Ye, Jifeng |
author_facet | Zheng, Yan Liu, Liwei Ye, Jifeng |
author_sort | Zheng, Yan |
collection | PubMed |
description | Type 1 diabetes is a prevalent autoimmune disease of which the underlying mechanisms remain to be elucidated. The aim of the study was to identify dysregulated modules of type 1 diabetes. After microarray data were preprocessed, 20,545 genes were obtained. By integrating gene expression data and protein-protein interactions (PPI) data, 48,778 new networks were obtained, including 7,953 genes. After simplifying networks, we obtained 24 target networks. By ranking networks with P-values, two modules with P<0.05 were identified, including the genes, CCNB1, CDC45, GINS2, NDC80, FBXO5, NCAPG and DLGAP5. Module 2 was part of module 1. The identified modules and genes may provide new insights into the underlying biological mechanisms that drive the progression of type 1 diabetes. |
format | Online Article Text |
id | pubmed-5841047 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-58410472018-03-15 Identification of dysregulated modules based on network entropy in type 1 diabetes Zheng, Yan Liu, Liwei Ye, Jifeng Exp Ther Med Articles Type 1 diabetes is a prevalent autoimmune disease of which the underlying mechanisms remain to be elucidated. The aim of the study was to identify dysregulated modules of type 1 diabetes. After microarray data were preprocessed, 20,545 genes were obtained. By integrating gene expression data and protein-protein interactions (PPI) data, 48,778 new networks were obtained, including 7,953 genes. After simplifying networks, we obtained 24 target networks. By ranking networks with P-values, two modules with P<0.05 were identified, including the genes, CCNB1, CDC45, GINS2, NDC80, FBXO5, NCAPG and DLGAP5. Module 2 was part of module 1. The identified modules and genes may provide new insights into the underlying biological mechanisms that drive the progression of type 1 diabetes. D.A. Spandidos 2018-04 2018-01-29 /pmc/articles/PMC5841047/ /pubmed/29545837 http://dx.doi.org/10.3892/etm.2018.5803 Text en Copyright: © Zheng 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 Zheng, Yan Liu, Liwei Ye, Jifeng Identification of dysregulated modules based on network entropy in type 1 diabetes |
title | Identification of dysregulated modules based on network entropy in type 1 diabetes |
title_full | Identification of dysregulated modules based on network entropy in type 1 diabetes |
title_fullStr | Identification of dysregulated modules based on network entropy in type 1 diabetes |
title_full_unstemmed | Identification of dysregulated modules based on network entropy in type 1 diabetes |
title_short | Identification of dysregulated modules based on network entropy in type 1 diabetes |
title_sort | identification of dysregulated modules based on network entropy in type 1 diabetes |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5841047/ https://www.ncbi.nlm.nih.gov/pubmed/29545837 http://dx.doi.org/10.3892/etm.2018.5803 |
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