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TRaCE+: Ensemble inference of gene regulatory networks from transcriptional expression profiles of gene knock-out experiments
BACKGROUND: The inference of gene regulatory networks (GRNs) from transcriptional expression profiles is challenging, predominantly due to its underdetermined nature. One important consequence of underdetermination is the existence of many possible solutions to this inference. Our previously propose...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4919846/ https://www.ncbi.nlm.nih.gov/pubmed/27342648 http://dx.doi.org/10.1186/s12859-016-1137-z |
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author | Ud-Dean, S.M. Minhaz Heise, Sandra Klamt, Steffen Gunawan, Rudiyanto |
author_facet | Ud-Dean, S.M. Minhaz Heise, Sandra Klamt, Steffen Gunawan, Rudiyanto |
author_sort | Ud-Dean, S.M. Minhaz |
collection | PubMed |
description | BACKGROUND: The inference of gene regulatory networks (GRNs) from transcriptional expression profiles is challenging, predominantly due to its underdetermined nature. One important consequence of underdetermination is the existence of many possible solutions to this inference. Our previously proposed ensemble inference algorithm TRaCE addressed this issue by inferring an ensemble of network directed graphs (digraphs) using differential gene expressions from gene knock-out (KO) experiments. However, TRaCE could not deal with the mode of the transcriptional regulations (activation or repression), an important feature of GRNs. RESULTS: In this work, we developed a new algorithm called TRaCE+ for the inference of an ensemble of signed GRN digraphs from transcriptional expression data of gene KO experiments. The sign of the edges indicates whether the regulation is an activation (positive) or a repression (negative). TRaCE+ generates the upper and lower bounds of the ensemble, which define uncertain regulatory interactions that could not be verified by the data. As demonstrated in the case studies using Escherichia coli GRN and 100-gene gold-standard GRNs from DREAM 4 network inference challenge, by accounting for regulatory signs, TRaCE+ could extract more information from the KO data than TRaCE, leading to fewer uncertain edges. Importantly, iterating TRaCE+ with an optimal design of gene KOs could resolve the underdetermined issue of GRN inference in much fewer KO experiments than using TRaCE. CONCLUSIONS: TRaCE+ expands the applications of ensemble GRN inference strategy by accounting for the mode of the gene regulatory interactions. In comparison to TRaCE, TRaCE+ enables a better utilization of gene KO data, thereby reducing the cost of tackling underdetermined GRN inference. TRaCE+ subroutines for MATLAB are freely available at the following website: http://www.cabsel.ethz.ch/tools/trace.html. |
format | Online Article Text |
id | pubmed-4919846 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-49198462016-06-28 TRaCE+: Ensemble inference of gene regulatory networks from transcriptional expression profiles of gene knock-out experiments Ud-Dean, S.M. Minhaz Heise, Sandra Klamt, Steffen Gunawan, Rudiyanto BMC Bioinformatics Methodology Article BACKGROUND: The inference of gene regulatory networks (GRNs) from transcriptional expression profiles is challenging, predominantly due to its underdetermined nature. One important consequence of underdetermination is the existence of many possible solutions to this inference. Our previously proposed ensemble inference algorithm TRaCE addressed this issue by inferring an ensemble of network directed graphs (digraphs) using differential gene expressions from gene knock-out (KO) experiments. However, TRaCE could not deal with the mode of the transcriptional regulations (activation or repression), an important feature of GRNs. RESULTS: In this work, we developed a new algorithm called TRaCE+ for the inference of an ensemble of signed GRN digraphs from transcriptional expression data of gene KO experiments. The sign of the edges indicates whether the regulation is an activation (positive) or a repression (negative). TRaCE+ generates the upper and lower bounds of the ensemble, which define uncertain regulatory interactions that could not be verified by the data. As demonstrated in the case studies using Escherichia coli GRN and 100-gene gold-standard GRNs from DREAM 4 network inference challenge, by accounting for regulatory signs, TRaCE+ could extract more information from the KO data than TRaCE, leading to fewer uncertain edges. Importantly, iterating TRaCE+ with an optimal design of gene KOs could resolve the underdetermined issue of GRN inference in much fewer KO experiments than using TRaCE. CONCLUSIONS: TRaCE+ expands the applications of ensemble GRN inference strategy by accounting for the mode of the gene regulatory interactions. In comparison to TRaCE, TRaCE+ enables a better utilization of gene KO data, thereby reducing the cost of tackling underdetermined GRN inference. TRaCE+ subroutines for MATLAB are freely available at the following website: http://www.cabsel.ethz.ch/tools/trace.html. BioMed Central 2016-06-24 /pmc/articles/PMC4919846/ /pubmed/27342648 http://dx.doi.org/10.1186/s12859-016-1137-z Text en © The Author(s). 2016 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 | Methodology Article Ud-Dean, S.M. Minhaz Heise, Sandra Klamt, Steffen Gunawan, Rudiyanto TRaCE+: Ensemble inference of gene regulatory networks from transcriptional expression profiles of gene knock-out experiments |
title | TRaCE+: Ensemble inference of gene regulatory networks from transcriptional expression profiles of gene knock-out experiments |
title_full | TRaCE+: Ensemble inference of gene regulatory networks from transcriptional expression profiles of gene knock-out experiments |
title_fullStr | TRaCE+: Ensemble inference of gene regulatory networks from transcriptional expression profiles of gene knock-out experiments |
title_full_unstemmed | TRaCE+: Ensemble inference of gene regulatory networks from transcriptional expression profiles of gene knock-out experiments |
title_short | TRaCE+: Ensemble inference of gene regulatory networks from transcriptional expression profiles of gene knock-out experiments |
title_sort | trace+: ensemble inference of gene regulatory networks from transcriptional expression profiles of gene knock-out experiments |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4919846/ https://www.ncbi.nlm.nih.gov/pubmed/27342648 http://dx.doi.org/10.1186/s12859-016-1137-z |
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