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Boolean network inference from time series data incorporating prior biological knowledge

BACKGROUND: Numerous approaches exist for modeling of genetic regulatory networks (GRNs) but the low sampling rates often employed in biological studies prevents the inference of detailed models from experimental data. In this paper, we analyze the issues involved in estimating a model of a GRN from...

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Autores principales: Haider, Saad, Pal, Ranadip
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3481452/
https://www.ncbi.nlm.nih.gov/pubmed/23134816
http://dx.doi.org/10.1186/1471-2164-13-S6-S9
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author Haider, Saad
Pal, Ranadip
author_facet Haider, Saad
Pal, Ranadip
author_sort Haider, Saad
collection PubMed
description BACKGROUND: Numerous approaches exist for modeling of genetic regulatory networks (GRNs) but the low sampling rates often employed in biological studies prevents the inference of detailed models from experimental data. In this paper, we analyze the issues involved in estimating a model of a GRN from single cell line time series data with limited time points. RESULTS: We present an inference approach for a Boolean Network (BN) model of a GRN from limited transcriptomic or proteomic time series data based on prior biological knowledge of connectivity, constraints on attractor structure and robust design. We applied our inference approach to 6 time point transcriptomic data on Human Mammary Epithelial Cell line (HMEC) after application of Epidermal Growth Factor (EGF) and generated a BN with a plausible biological structure satisfying the data. We further defined and applied a similarity measure to compare synthetic BNs and BNs generated through the proposed approach constructed from transitions of various paths of the synthetic BNs. We have also compared the performance of our algorithm with two existing BN inference algorithms. CONCLUSIONS: Through theoretical analysis and simulations, we showed the rarity of arriving at a BN from limited time series data with plausible biological structure using random connectivity and absence of structure in data. The framework when applied to experimental data and data generated from synthetic BNs were able to estimate BNs with high similarity scores. Comparison with existing BN inference algorithms showed the better performance of our proposed algorithm for limited time series data. The proposed framework can also be applied to optimize the connectivity of a GRN from experimental data when the prior biological knowledge on regulators is limited or not unique.
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spelling pubmed-34814522012-11-02 Boolean network inference from time series data incorporating prior biological knowledge Haider, Saad Pal, Ranadip BMC Genomics Research BACKGROUND: Numerous approaches exist for modeling of genetic regulatory networks (GRNs) but the low sampling rates often employed in biological studies prevents the inference of detailed models from experimental data. In this paper, we analyze the issues involved in estimating a model of a GRN from single cell line time series data with limited time points. RESULTS: We present an inference approach for a Boolean Network (BN) model of a GRN from limited transcriptomic or proteomic time series data based on prior biological knowledge of connectivity, constraints on attractor structure and robust design. We applied our inference approach to 6 time point transcriptomic data on Human Mammary Epithelial Cell line (HMEC) after application of Epidermal Growth Factor (EGF) and generated a BN with a plausible biological structure satisfying the data. We further defined and applied a similarity measure to compare synthetic BNs and BNs generated through the proposed approach constructed from transitions of various paths of the synthetic BNs. We have also compared the performance of our algorithm with two existing BN inference algorithms. CONCLUSIONS: Through theoretical analysis and simulations, we showed the rarity of arriving at a BN from limited time series data with plausible biological structure using random connectivity and absence of structure in data. The framework when applied to experimental data and data generated from synthetic BNs were able to estimate BNs with high similarity scores. Comparison with existing BN inference algorithms showed the better performance of our proposed algorithm for limited time series data. The proposed framework can also be applied to optimize the connectivity of a GRN from experimental data when the prior biological knowledge on regulators is limited or not unique. BioMed Central 2012-10-26 /pmc/articles/PMC3481452/ /pubmed/23134816 http://dx.doi.org/10.1186/1471-2164-13-S6-S9 Text en Copyright ©2012 Haider and Pal; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Haider, Saad
Pal, Ranadip
Boolean network inference from time series data incorporating prior biological knowledge
title Boolean network inference from time series data incorporating prior biological knowledge
title_full Boolean network inference from time series data incorporating prior biological knowledge
title_fullStr Boolean network inference from time series data incorporating prior biological knowledge
title_full_unstemmed Boolean network inference from time series data incorporating prior biological knowledge
title_short Boolean network inference from time series data incorporating prior biological knowledge
title_sort boolean network inference from time series data incorporating prior biological knowledge
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3481452/
https://www.ncbi.nlm.nih.gov/pubmed/23134816
http://dx.doi.org/10.1186/1471-2164-13-S6-S9
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