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Inferring interaction type in gene regulatory networks using co-expression data
BACKGROUND: Knowledge of interaction types in biological networks is important for understanding the functional organization of the cell. Currently information-based approaches are widely used for inferring gene regulatory interactions from genomics data, such as gene expression profiles; however, t...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4495944/ https://www.ncbi.nlm.nih.gov/pubmed/26157474 http://dx.doi.org/10.1186/s13015-015-0054-4 |
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author | Khosravi, Pegah Gazestani, Vahid H Pirhaji, Leila Law, Brian Sadeghi, Mehdi Goliaei, Bahram Bader, Gary D |
author_facet | Khosravi, Pegah Gazestani, Vahid H Pirhaji, Leila Law, Brian Sadeghi, Mehdi Goliaei, Bahram Bader, Gary D |
author_sort | Khosravi, Pegah |
collection | PubMed |
description | BACKGROUND: Knowledge of interaction types in biological networks is important for understanding the functional organization of the cell. Currently information-based approaches are widely used for inferring gene regulatory interactions from genomics data, such as gene expression profiles; however, these approaches do not provide evidence about the regulation type (positive or negative sign) of the interaction. RESULTS: This paper describes a novel algorithm, “Signing of Regulatory Networks” (SIREN), which can infer the regulatory type of interactions in a known gene regulatory network (GRN) given corresponding genome-wide gene expression data. To assess our new approach, we applied it to three different benchmark gene regulatory networks, including Escherichia coli, prostate cancer, and an in silico constructed network. Our new method has approximately 68, 70, and 100 percent accuracy, respectively, for these networks. To showcase the utility of SIREN algorithm, we used it to predict previously unknown regulation types for 454 interactions related to the prostate cancer GRN. CONCLUSIONS: SIREN is an efficient algorithm with low computational complexity; hence, it is applicable to large biological networks. It can serve as a complementary approach for a wide range of network reconstruction methods that do not provide information about the interaction type. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13015-015-0054-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4495944 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-44959442015-07-09 Inferring interaction type in gene regulatory networks using co-expression data Khosravi, Pegah Gazestani, Vahid H Pirhaji, Leila Law, Brian Sadeghi, Mehdi Goliaei, Bahram Bader, Gary D Algorithms Mol Biol Research BACKGROUND: Knowledge of interaction types in biological networks is important for understanding the functional organization of the cell. Currently information-based approaches are widely used for inferring gene regulatory interactions from genomics data, such as gene expression profiles; however, these approaches do not provide evidence about the regulation type (positive or negative sign) of the interaction. RESULTS: This paper describes a novel algorithm, “Signing of Regulatory Networks” (SIREN), which can infer the regulatory type of interactions in a known gene regulatory network (GRN) given corresponding genome-wide gene expression data. To assess our new approach, we applied it to three different benchmark gene regulatory networks, including Escherichia coli, prostate cancer, and an in silico constructed network. Our new method has approximately 68, 70, and 100 percent accuracy, respectively, for these networks. To showcase the utility of SIREN algorithm, we used it to predict previously unknown regulation types for 454 interactions related to the prostate cancer GRN. CONCLUSIONS: SIREN is an efficient algorithm with low computational complexity; hence, it is applicable to large biological networks. It can serve as a complementary approach for a wide range of network reconstruction methods that do not provide information about the interaction type. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13015-015-0054-4) contains supplementary material, which is available to authorized users. BioMed Central 2015-07-08 /pmc/articles/PMC4495944/ /pubmed/26157474 http://dx.doi.org/10.1186/s13015-015-0054-4 Text en © Khosravi et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Khosravi, Pegah Gazestani, Vahid H Pirhaji, Leila Law, Brian Sadeghi, Mehdi Goliaei, Bahram Bader, Gary D Inferring interaction type in gene regulatory networks using co-expression data |
title | Inferring interaction type in gene regulatory networks using co-expression data |
title_full | Inferring interaction type in gene regulatory networks using co-expression data |
title_fullStr | Inferring interaction type in gene regulatory networks using co-expression data |
title_full_unstemmed | Inferring interaction type in gene regulatory networks using co-expression data |
title_short | Inferring interaction type in gene regulatory networks using co-expression data |
title_sort | inferring interaction type in gene regulatory networks using co-expression data |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4495944/ https://www.ncbi.nlm.nih.gov/pubmed/26157474 http://dx.doi.org/10.1186/s13015-015-0054-4 |
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