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IGSA: Individual Gene Sets Analysis, including Enrichment and Clustering
Analysis of gene sets has been widely applied in various high-throughput biological studies. One weakness in the traditional methods is that they neglect the heterogeneity of genes expressions in samples which may lead to the omission of some specific and important gene sets. It is also difficult fo...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5072653/ https://www.ncbi.nlm.nih.gov/pubmed/27764138 http://dx.doi.org/10.1371/journal.pone.0164542 |
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author | Wu, Lingxiang Chen, Xiujie Zhang, Denan Zhang, Wubing Liu, Lei Ma, Hongzhe Yang, Jingbo Xie, Hongbo Liu, Bo Jin, Qing |
author_facet | Wu, Lingxiang Chen, Xiujie Zhang, Denan Zhang, Wubing Liu, Lei Ma, Hongzhe Yang, Jingbo Xie, Hongbo Liu, Bo Jin, Qing |
author_sort | Wu, Lingxiang |
collection | PubMed |
description | Analysis of gene sets has been widely applied in various high-throughput biological studies. One weakness in the traditional methods is that they neglect the heterogeneity of genes expressions in samples which may lead to the omission of some specific and important gene sets. It is also difficult for them to reflect the severities of disease and provide expression profiles of gene sets for individuals. We developed an application software called IGSA that leverages a powerful analytical capacity in gene sets enrichment and samples clustering. IGSA calculates gene sets expression scores for each sample and takes an accumulating clustering strategy to let the samples gather into the set according to the progress of disease from mild to severe. We focus on gastric, pancreatic and ovarian cancer data sets for the performance of IGSA. We also compared the results of IGSA in KEGG pathways enrichment with David, GSEA, SPIA, ssGSEA and analyzed the results of IGSA clustering and different similarity measurement methods. Notably, IGSA is proved to be more sensitive and specific in finding significant pathways, and can indicate related changes in pathways with the severity of disease. In addition, IGSA provides with significant gene sets profile for each sample. |
format | Online Article Text |
id | pubmed-5072653 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-50726532016-10-27 IGSA: Individual Gene Sets Analysis, including Enrichment and Clustering Wu, Lingxiang Chen, Xiujie Zhang, Denan Zhang, Wubing Liu, Lei Ma, Hongzhe Yang, Jingbo Xie, Hongbo Liu, Bo Jin, Qing PLoS One Research Article Analysis of gene sets has been widely applied in various high-throughput biological studies. One weakness in the traditional methods is that they neglect the heterogeneity of genes expressions in samples which may lead to the omission of some specific and important gene sets. It is also difficult for them to reflect the severities of disease and provide expression profiles of gene sets for individuals. We developed an application software called IGSA that leverages a powerful analytical capacity in gene sets enrichment and samples clustering. IGSA calculates gene sets expression scores for each sample and takes an accumulating clustering strategy to let the samples gather into the set according to the progress of disease from mild to severe. We focus on gastric, pancreatic and ovarian cancer data sets for the performance of IGSA. We also compared the results of IGSA in KEGG pathways enrichment with David, GSEA, SPIA, ssGSEA and analyzed the results of IGSA clustering and different similarity measurement methods. Notably, IGSA is proved to be more sensitive and specific in finding significant pathways, and can indicate related changes in pathways with the severity of disease. In addition, IGSA provides with significant gene sets profile for each sample. Public Library of Science 2016-10-20 /pmc/articles/PMC5072653/ /pubmed/27764138 http://dx.doi.org/10.1371/journal.pone.0164542 Text en © 2016 Wu et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Wu, Lingxiang Chen, Xiujie Zhang, Denan Zhang, Wubing Liu, Lei Ma, Hongzhe Yang, Jingbo Xie, Hongbo Liu, Bo Jin, Qing IGSA: Individual Gene Sets Analysis, including Enrichment and Clustering |
title | IGSA: Individual Gene Sets Analysis, including Enrichment and Clustering |
title_full | IGSA: Individual Gene Sets Analysis, including Enrichment and Clustering |
title_fullStr | IGSA: Individual Gene Sets Analysis, including Enrichment and Clustering |
title_full_unstemmed | IGSA: Individual Gene Sets Analysis, including Enrichment and Clustering |
title_short | IGSA: Individual Gene Sets Analysis, including Enrichment and Clustering |
title_sort | igsa: individual gene sets analysis, including enrichment and clustering |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5072653/ https://www.ncbi.nlm.nih.gov/pubmed/27764138 http://dx.doi.org/10.1371/journal.pone.0164542 |
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