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Open Data for Differential Network Analysis in Glioma
The complexity of cancer diseases demands bioinformatic techniques and translational research based on big data and personalized medicine. Open data enables researchers to accelerate cancer studies, save resources and foster collaboration. Several tools and programming approaches are available for a...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7013918/ https://www.ncbi.nlm.nih.gov/pubmed/31952211 http://dx.doi.org/10.3390/ijms21020547 |
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author | Jean-Quartier, Claire Jeanquartier, Fleur Holzinger, Andreas |
author_facet | Jean-Quartier, Claire Jeanquartier, Fleur Holzinger, Andreas |
author_sort | Jean-Quartier, Claire |
collection | PubMed |
description | The complexity of cancer diseases demands bioinformatic techniques and translational research based on big data and personalized medicine. Open data enables researchers to accelerate cancer studies, save resources and foster collaboration. Several tools and programming approaches are available for analyzing data, including annotation, clustering, comparison and extrapolation, merging, enrichment, functional association and statistics. We exploit openly available data via cancer gene expression analysis, we apply refinement as well as enrichment analysis via gene ontology and conclude with graph-based visualization of involved protein interaction networks as a basis for signaling. The different databases allowed for the construction of huge networks or specified ones consisting of high-confidence interactions only. Several genes associated to glioma were isolated via a network analysis from top hub nodes as well as from an outlier analysis. The latter approach highlights a mitogen-activated protein kinase next to a member of histondeacetylases and a protein phosphatase as genes uncommonly associated with glioma. Cluster analysis from top hub nodes lists several identified glioma-associated gene products to function within protein complexes, including epidermal growth factors as well as cell cycle proteins or RAS proto-oncogenes. By using selected exemplary tools and open-access resources for cancer research and differential network analysis, we highlight disturbed signaling components in brain cancer subtypes of glioma. |
format | Online Article Text |
id | pubmed-7013918 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-70139182020-03-09 Open Data for Differential Network Analysis in Glioma Jean-Quartier, Claire Jeanquartier, Fleur Holzinger, Andreas Int J Mol Sci Article The complexity of cancer diseases demands bioinformatic techniques and translational research based on big data and personalized medicine. Open data enables researchers to accelerate cancer studies, save resources and foster collaboration. Several tools and programming approaches are available for analyzing data, including annotation, clustering, comparison and extrapolation, merging, enrichment, functional association and statistics. We exploit openly available data via cancer gene expression analysis, we apply refinement as well as enrichment analysis via gene ontology and conclude with graph-based visualization of involved protein interaction networks as a basis for signaling. The different databases allowed for the construction of huge networks or specified ones consisting of high-confidence interactions only. Several genes associated to glioma were isolated via a network analysis from top hub nodes as well as from an outlier analysis. The latter approach highlights a mitogen-activated protein kinase next to a member of histondeacetylases and a protein phosphatase as genes uncommonly associated with glioma. Cluster analysis from top hub nodes lists several identified glioma-associated gene products to function within protein complexes, including epidermal growth factors as well as cell cycle proteins or RAS proto-oncogenes. By using selected exemplary tools and open-access resources for cancer research and differential network analysis, we highlight disturbed signaling components in brain cancer subtypes of glioma. MDPI 2020-01-15 /pmc/articles/PMC7013918/ /pubmed/31952211 http://dx.doi.org/10.3390/ijms21020547 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Jean-Quartier, Claire Jeanquartier, Fleur Holzinger, Andreas Open Data for Differential Network Analysis in Glioma |
title | Open Data for Differential Network Analysis in Glioma |
title_full | Open Data for Differential Network Analysis in Glioma |
title_fullStr | Open Data for Differential Network Analysis in Glioma |
title_full_unstemmed | Open Data for Differential Network Analysis in Glioma |
title_short | Open Data for Differential Network Analysis in Glioma |
title_sort | open data for differential network analysis in glioma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7013918/ https://www.ncbi.nlm.nih.gov/pubmed/31952211 http://dx.doi.org/10.3390/ijms21020547 |
work_keys_str_mv | AT jeanquartierclaire opendatafordifferentialnetworkanalysisinglioma AT jeanquartierfleur opendatafordifferentialnetworkanalysisinglioma AT holzingerandreas opendatafordifferentialnetworkanalysisinglioma |