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Knowledge of the perturbation design is essential for accurate gene regulatory network inference

The gene regulatory network (GRN) of a cell executes genetic programs in response to environmental and internal cues. Two distinct classes of methods are used to infer regulatory interactions from gene expression: those that only use observed changes in gene expression, and those that use both the o...

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Autores principales: Seçilmiş, Deniz, Hillerton, Thomas, Tjärnberg, Andreas, Nelander, Sven, Nordling, Torbjörn E. M., Sonnhammer, Erik L. L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9529923/
https://www.ncbi.nlm.nih.gov/pubmed/36192495
http://dx.doi.org/10.1038/s41598-022-19005-x
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author Seçilmiş, Deniz
Hillerton, Thomas
Tjärnberg, Andreas
Nelander, Sven
Nordling, Torbjörn E. M.
Sonnhammer, Erik L. L.
author_facet Seçilmiş, Deniz
Hillerton, Thomas
Tjärnberg, Andreas
Nelander, Sven
Nordling, Torbjörn E. M.
Sonnhammer, Erik L. L.
author_sort Seçilmiş, Deniz
collection PubMed
description The gene regulatory network (GRN) of a cell executes genetic programs in response to environmental and internal cues. Two distinct classes of methods are used to infer regulatory interactions from gene expression: those that only use observed changes in gene expression, and those that use both the observed changes and the perturbation design, i.e. the targets used to cause the changes in gene expression. Considering that the GRN by definition converts input cues to changes in gene expression, it may be conjectured that the latter methods would yield more accurate inferences but this has not previously been investigated. To address this question, we evaluated a number of popular GRN inference methods that either use the perturbation design or not. For the evaluation we used targeted perturbation knockdown gene expression datasets with varying noise levels generated by two different packages, GeneNetWeaver and GeneSpider. The accuracy was evaluated on each dataset using a variety of measures. The results show that on all datasets, methods using the perturbation design matrix consistently and significantly outperform methods not using it. This was also found to be the case on a smaller experimental dataset from E. coli. Targeted gene perturbations combined with inference methods that use the perturbation design are indispensable for accurate GRN inference.
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spelling pubmed-95299232022-10-05 Knowledge of the perturbation design is essential for accurate gene regulatory network inference Seçilmiş, Deniz Hillerton, Thomas Tjärnberg, Andreas Nelander, Sven Nordling, Torbjörn E. M. Sonnhammer, Erik L. L. Sci Rep Article The gene regulatory network (GRN) of a cell executes genetic programs in response to environmental and internal cues. Two distinct classes of methods are used to infer regulatory interactions from gene expression: those that only use observed changes in gene expression, and those that use both the observed changes and the perturbation design, i.e. the targets used to cause the changes in gene expression. Considering that the GRN by definition converts input cues to changes in gene expression, it may be conjectured that the latter methods would yield more accurate inferences but this has not previously been investigated. To address this question, we evaluated a number of popular GRN inference methods that either use the perturbation design or not. For the evaluation we used targeted perturbation knockdown gene expression datasets with varying noise levels generated by two different packages, GeneNetWeaver and GeneSpider. The accuracy was evaluated on each dataset using a variety of measures. The results show that on all datasets, methods using the perturbation design matrix consistently and significantly outperform methods not using it. This was also found to be the case on a smaller experimental dataset from E. coli. Targeted gene perturbations combined with inference methods that use the perturbation design are indispensable for accurate GRN inference. Nature Publishing Group UK 2022-10-03 /pmc/articles/PMC9529923/ /pubmed/36192495 http://dx.doi.org/10.1038/s41598-022-19005-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Seçilmiş, Deniz
Hillerton, Thomas
Tjärnberg, Andreas
Nelander, Sven
Nordling, Torbjörn E. M.
Sonnhammer, Erik L. L.
Knowledge of the perturbation design is essential for accurate gene regulatory network inference
title Knowledge of the perturbation design is essential for accurate gene regulatory network inference
title_full Knowledge of the perturbation design is essential for accurate gene regulatory network inference
title_fullStr Knowledge of the perturbation design is essential for accurate gene regulatory network inference
title_full_unstemmed Knowledge of the perturbation design is essential for accurate gene regulatory network inference
title_short Knowledge of the perturbation design is essential for accurate gene regulatory network inference
title_sort knowledge of the perturbation design is essential for accurate gene regulatory network inference
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9529923/
https://www.ncbi.nlm.nih.gov/pubmed/36192495
http://dx.doi.org/10.1038/s41598-022-19005-x
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