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PAGER 2.0: an update to the pathway, annotated-list and gene-signature electronic repository for Human Network Biology
Integrative Gene-set, Network and Pathway Analysis (GNPA) is a powerful data analysis approach developed to help interpret high-throughput omics data. In PAGER 1.0, we demonstrated that researchers can gain unbiased and reproducible biological insights with the introduction of PAGs (Pathways, Annota...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5753198/ https://www.ncbi.nlm.nih.gov/pubmed/29126216 http://dx.doi.org/10.1093/nar/gkx1040 |
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author | Yue, Zongliang Zheng, Qi Neylon, Michael T Yoo, Minjae Shin, Jimin Zhao, Zhiying Tan, Aik Choon Chen, Jake Y |
author_facet | Yue, Zongliang Zheng, Qi Neylon, Michael T Yoo, Minjae Shin, Jimin Zhao, Zhiying Tan, Aik Choon Chen, Jake Y |
author_sort | Yue, Zongliang |
collection | PubMed |
description | Integrative Gene-set, Network and Pathway Analysis (GNPA) is a powerful data analysis approach developed to help interpret high-throughput omics data. In PAGER 1.0, we demonstrated that researchers can gain unbiased and reproducible biological insights with the introduction of PAGs (Pathways, Annotated-lists and Gene-signatures) as the basic data representation elements. In PAGER 2.0, we improve the utility of integrative GNPA by significantly expanding the coverage of PAGs and PAG-to-PAG relationships in the database, defining a new metric to quantify PAG data qualities, and developing new software features to simplify online integrative GNPA. Specifically, we included 84 282 PAGs spanning 24 different data sources that cover human diseases, published gene-expression signatures, drug–gene, miRNA–gene interactions, pathways and tissue-specific gene expressions. We introduced a new normalized Cohesion Coefficient (nCoCo) score to assess the biological relevance of genes inside a PAG, and RP-score to rank genes and assign gene-specific weights inside a PAG. The companion web interface contains numerous features to help users query and navigate the database content. The database content can be freely downloaded and is compatible with third-party Gene Set Enrichment Analysis tools. We expect PAGER 2.0 to become a major resource in integrative GNPA. PAGER 2.0 is available at http://discovery.informatics.uab.edu/PAGER/. |
format | Online Article Text |
id | pubmed-5753198 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-57531982018-01-05 PAGER 2.0: an update to the pathway, annotated-list and gene-signature electronic repository for Human Network Biology Yue, Zongliang Zheng, Qi Neylon, Michael T Yoo, Minjae Shin, Jimin Zhao, Zhiying Tan, Aik Choon Chen, Jake Y Nucleic Acids Res Database Issue Integrative Gene-set, Network and Pathway Analysis (GNPA) is a powerful data analysis approach developed to help interpret high-throughput omics data. In PAGER 1.0, we demonstrated that researchers can gain unbiased and reproducible biological insights with the introduction of PAGs (Pathways, Annotated-lists and Gene-signatures) as the basic data representation elements. In PAGER 2.0, we improve the utility of integrative GNPA by significantly expanding the coverage of PAGs and PAG-to-PAG relationships in the database, defining a new metric to quantify PAG data qualities, and developing new software features to simplify online integrative GNPA. Specifically, we included 84 282 PAGs spanning 24 different data sources that cover human diseases, published gene-expression signatures, drug–gene, miRNA–gene interactions, pathways and tissue-specific gene expressions. We introduced a new normalized Cohesion Coefficient (nCoCo) score to assess the biological relevance of genes inside a PAG, and RP-score to rank genes and assign gene-specific weights inside a PAG. The companion web interface contains numerous features to help users query and navigate the database content. The database content can be freely downloaded and is compatible with third-party Gene Set Enrichment Analysis tools. We expect PAGER 2.0 to become a major resource in integrative GNPA. PAGER 2.0 is available at http://discovery.informatics.uab.edu/PAGER/. Oxford University Press 2018-01-04 2017-11-08 /pmc/articles/PMC5753198/ /pubmed/29126216 http://dx.doi.org/10.1093/nar/gkx1040 Text en © The Author(s) 2017. Published by Oxford University Press on behalf of Nucleic Acids Research. 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Database Issue Yue, Zongliang Zheng, Qi Neylon, Michael T Yoo, Minjae Shin, Jimin Zhao, Zhiying Tan, Aik Choon Chen, Jake Y PAGER 2.0: an update to the pathway, annotated-list and gene-signature electronic repository for Human Network Biology |
title | PAGER 2.0: an update to the pathway, annotated-list and gene-signature electronic repository for Human Network Biology |
title_full | PAGER 2.0: an update to the pathway, annotated-list and gene-signature electronic repository for Human Network Biology |
title_fullStr | PAGER 2.0: an update to the pathway, annotated-list and gene-signature electronic repository for Human Network Biology |
title_full_unstemmed | PAGER 2.0: an update to the pathway, annotated-list and gene-signature electronic repository for Human Network Biology |
title_short | PAGER 2.0: an update to the pathway, annotated-list and gene-signature electronic repository for Human Network Biology |
title_sort | pager 2.0: an update to the pathway, annotated-list and gene-signature electronic repository for human network biology |
topic | Database Issue |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5753198/ https://www.ncbi.nlm.nih.gov/pubmed/29126216 http://dx.doi.org/10.1093/nar/gkx1040 |
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