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Intrinsically Bayesian robust classifier for single-cell gene expression trajectories in gene regulatory networks
BACKGROUND: Expression-based phenotype classification using either microarray or RNA-Seq measurements suffers from a lack of specificity because pathway timing is not revealed and expressions are averaged across groups of cells. This paper studies expression-based classification under the assumption...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5872504/ https://www.ncbi.nlm.nih.gov/pubmed/29589564 http://dx.doi.org/10.1186/s12918-018-0549-y |
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author | Karbalayghareh, Alireza Braga-Neto, Ulisses Dougherty, Edward R. |
author_facet | Karbalayghareh, Alireza Braga-Neto, Ulisses Dougherty, Edward R. |
author_sort | Karbalayghareh, Alireza |
collection | PubMed |
description | BACKGROUND: Expression-based phenotype classification using either microarray or RNA-Seq measurements suffers from a lack of specificity because pathway timing is not revealed and expressions are averaged across groups of cells. This paper studies expression-based classification under the assumption that single-cell measurements are sampled at a sufficient rate to detect regulatory timing. Thus, observations are expression trajectories. In effect, classification is performed on data generated by an underlying gene regulatory network. RESULTS: Network regulation is modeled via a Boolean network with perturbation, regulation not fully determined owing to inherent biological randomness. The binary assumption is not critical because the resulting Markov chain characterizes expression trajectories. We assume a partially known Gaussian observation model belonging to an uncertainty class of models. We derive the intrinsically Bayesian robust classifier to discriminate between wild-type and mutated networks based on expression trajectories. The classifier minimizes the expected error across the uncertainty class relative to the prior distribution. We test it using a mammalian cell-cycle model, discriminating between the normal network and one in which gene p27 is mutated, thereby producing a cancerous phenotype. Tests examine all model aspects, including trajectory length, perturbation probability, and the hyperparameters governing the prior distribution over the uncertainty class. CONCLUSIONS: Simulations show the rates at which the expected error is diminished by smaller perturbation probability, longer trajectories, and hyperparameters that tighten the prior distribution relative to the unknown true network. For average-expression measurement, methods have been proposed to obtain prior distributions. These should be extended to the more mathematically difficult, but more informative, expression trajectories. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12918-018-0549-y) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5872504 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-58725042018-04-02 Intrinsically Bayesian robust classifier for single-cell gene expression trajectories in gene regulatory networks Karbalayghareh, Alireza Braga-Neto, Ulisses Dougherty, Edward R. BMC Syst Biol Research BACKGROUND: Expression-based phenotype classification using either microarray or RNA-Seq measurements suffers from a lack of specificity because pathway timing is not revealed and expressions are averaged across groups of cells. This paper studies expression-based classification under the assumption that single-cell measurements are sampled at a sufficient rate to detect regulatory timing. Thus, observations are expression trajectories. In effect, classification is performed on data generated by an underlying gene regulatory network. RESULTS: Network regulation is modeled via a Boolean network with perturbation, regulation not fully determined owing to inherent biological randomness. The binary assumption is not critical because the resulting Markov chain characterizes expression trajectories. We assume a partially known Gaussian observation model belonging to an uncertainty class of models. We derive the intrinsically Bayesian robust classifier to discriminate between wild-type and mutated networks based on expression trajectories. The classifier minimizes the expected error across the uncertainty class relative to the prior distribution. We test it using a mammalian cell-cycle model, discriminating between the normal network and one in which gene p27 is mutated, thereby producing a cancerous phenotype. Tests examine all model aspects, including trajectory length, perturbation probability, and the hyperparameters governing the prior distribution over the uncertainty class. CONCLUSIONS: Simulations show the rates at which the expected error is diminished by smaller perturbation probability, longer trajectories, and hyperparameters that tighten the prior distribution relative to the unknown true network. For average-expression measurement, methods have been proposed to obtain prior distributions. These should be extended to the more mathematically difficult, but more informative, expression trajectories. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12918-018-0549-y) contains supplementary material, which is available to authorized users. BioMed Central 2018-03-21 /pmc/articles/PMC5872504/ /pubmed/29589564 http://dx.doi.org/10.1186/s12918-018-0549-y Text en © The Author(s) 2018 Open Access This 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 Karbalayghareh, Alireza Braga-Neto, Ulisses Dougherty, Edward R. Intrinsically Bayesian robust classifier for single-cell gene expression trajectories in gene regulatory networks |
title | Intrinsically Bayesian robust classifier for single-cell gene expression trajectories in gene regulatory networks |
title_full | Intrinsically Bayesian robust classifier for single-cell gene expression trajectories in gene regulatory networks |
title_fullStr | Intrinsically Bayesian robust classifier for single-cell gene expression trajectories in gene regulatory networks |
title_full_unstemmed | Intrinsically Bayesian robust classifier for single-cell gene expression trajectories in gene regulatory networks |
title_short | Intrinsically Bayesian robust classifier for single-cell gene expression trajectories in gene regulatory networks |
title_sort | intrinsically bayesian robust classifier for single-cell gene expression trajectories in gene regulatory networks |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5872504/ https://www.ncbi.nlm.nih.gov/pubmed/29589564 http://dx.doi.org/10.1186/s12918-018-0549-y |
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