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Integrating gene regulatory pathways into differential network analysis of gene expression data
The advent of next-generation sequencing has introduced new opportunities in analyzing gene expression data. Research in systems biology has taken advantage of these opportunities by gleaning insights into gene regulatory networks through the analysis of gene association networks. Contrasting networ...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6445151/ https://www.ncbi.nlm.nih.gov/pubmed/30940863 http://dx.doi.org/10.1038/s41598-019-41918-3 |
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author | Grimes, Tyler Potter, S. Steven Datta, Somnath |
author_facet | Grimes, Tyler Potter, S. Steven Datta, Somnath |
author_sort | Grimes, Tyler |
collection | PubMed |
description | The advent of next-generation sequencing has introduced new opportunities in analyzing gene expression data. Research in systems biology has taken advantage of these opportunities by gleaning insights into gene regulatory networks through the analysis of gene association networks. Contrasting networks from different populations can reveal the many different roles genes fill, which can lead to new discoveries in gene function. Pathologies can also arise from aberrations in these gene-gene interactions. Exposing these network irregularities provides a new avenue for understanding and treating diseases. A general framework for integrating known gene regulatory pathways into a differential network analysis between two populations is proposed. The framework importantly allows for any gene-gene association measure to be used, and inference is carried out through permutation testing. A simulation study investigates the performance in identifying differentially connected genes when incorporating known pathways, even if the pathway knowledge is partially inaccurate. Another simulation study compares the general framework with four state-of-the-art methods. Two RNA-seq datasets are analyzed to illustrate the use of this framework in practice. In both examples, the analysis reveals genes and pathways that are known to be biologically significant along with potentially novel findings that may be used to motivate future research. |
format | Online Article Text |
id | pubmed-6445151 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64451512019-04-05 Integrating gene regulatory pathways into differential network analysis of gene expression data Grimes, Tyler Potter, S. Steven Datta, Somnath Sci Rep Article The advent of next-generation sequencing has introduced new opportunities in analyzing gene expression data. Research in systems biology has taken advantage of these opportunities by gleaning insights into gene regulatory networks through the analysis of gene association networks. Contrasting networks from different populations can reveal the many different roles genes fill, which can lead to new discoveries in gene function. Pathologies can also arise from aberrations in these gene-gene interactions. Exposing these network irregularities provides a new avenue for understanding and treating diseases. A general framework for integrating known gene regulatory pathways into a differential network analysis between two populations is proposed. The framework importantly allows for any gene-gene association measure to be used, and inference is carried out through permutation testing. A simulation study investigates the performance in identifying differentially connected genes when incorporating known pathways, even if the pathway knowledge is partially inaccurate. Another simulation study compares the general framework with four state-of-the-art methods. Two RNA-seq datasets are analyzed to illustrate the use of this framework in practice. In both examples, the analysis reveals genes and pathways that are known to be biologically significant along with potentially novel findings that may be used to motivate future research. Nature Publishing Group UK 2019-04-02 /pmc/articles/PMC6445151/ /pubmed/30940863 http://dx.doi.org/10.1038/s41598-019-41918-3 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Grimes, Tyler Potter, S. Steven Datta, Somnath Integrating gene regulatory pathways into differential network analysis of gene expression data |
title | Integrating gene regulatory pathways into differential network analysis of gene expression data |
title_full | Integrating gene regulatory pathways into differential network analysis of gene expression data |
title_fullStr | Integrating gene regulatory pathways into differential network analysis of gene expression data |
title_full_unstemmed | Integrating gene regulatory pathways into differential network analysis of gene expression data |
title_short | Integrating gene regulatory pathways into differential network analysis of gene expression data |
title_sort | integrating gene regulatory pathways into differential network analysis of gene expression data |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6445151/ https://www.ncbi.nlm.nih.gov/pubmed/30940863 http://dx.doi.org/10.1038/s41598-019-41918-3 |
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