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Gene network reconstruction from transcriptional dynamics under kinetic model uncertainty: a case for the second derivative

Motivation: Measurements of gene expression over time enable the reconstruction of transcriptional networks. However, Bayesian networks and many other current reconstruction methods rely on assumptions that conflict with the differential equations that describe transcriptional kinetics. Practical ap...

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Autores principales: Bickel, David R., Montazeri, Zahra, Hsieh, Pei-Chun, Beatty, Mary, Lawit, Shai J., Bate, Nicholas J.
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2654806/
https://www.ncbi.nlm.nih.gov/pubmed/19218351
http://dx.doi.org/10.1093/bioinformatics/btp028
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author Bickel, David R.
Montazeri, Zahra
Hsieh, Pei-Chun
Beatty, Mary
Lawit, Shai J.
Bate, Nicholas J.
author_facet Bickel, David R.
Montazeri, Zahra
Hsieh, Pei-Chun
Beatty, Mary
Lawit, Shai J.
Bate, Nicholas J.
author_sort Bickel, David R.
collection PubMed
description Motivation: Measurements of gene expression over time enable the reconstruction of transcriptional networks. However, Bayesian networks and many other current reconstruction methods rely on assumptions that conflict with the differential equations that describe transcriptional kinetics. Practical approximations of kinetic models would enable inferring causal relationships between genes from expression data of microarray, tag-based and conventional platforms, but conclusions are sensitive to the assumptions made. Results: The representation of a sufficiently large portion of genome enables computation of an upper bound on how much confidence one may place in influences between genes on the basis of expression data. Information about which genes encode transcription factors is not necessary but may be incorporated if available. The methodology is generalized to cover cases in which expression measurements are missing for many of the genes that might control the transcription of the genes of interest. The assumption that the gene expression level is roughly proportional to the rate of translation led to better empirical performance than did either the assumption that the gene expression level is roughly proportional to the protein level or the Bayesian model average of both assumptions. Availability: http://www.oisb.ca points to R code implementing the methods (R Development Core Team 2004). Contact: dbickel@uottawa.ca Supplementary information: http://www.davidbickel.com
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spelling pubmed-26548062009-04-02 Gene network reconstruction from transcriptional dynamics under kinetic model uncertainty: a case for the second derivative Bickel, David R. Montazeri, Zahra Hsieh, Pei-Chun Beatty, Mary Lawit, Shai J. Bate, Nicholas J. Bioinformatics Original Papers Motivation: Measurements of gene expression over time enable the reconstruction of transcriptional networks. However, Bayesian networks and many other current reconstruction methods rely on assumptions that conflict with the differential equations that describe transcriptional kinetics. Practical approximations of kinetic models would enable inferring causal relationships between genes from expression data of microarray, tag-based and conventional platforms, but conclusions are sensitive to the assumptions made. Results: The representation of a sufficiently large portion of genome enables computation of an upper bound on how much confidence one may place in influences between genes on the basis of expression data. Information about which genes encode transcription factors is not necessary but may be incorporated if available. The methodology is generalized to cover cases in which expression measurements are missing for many of the genes that might control the transcription of the genes of interest. The assumption that the gene expression level is roughly proportional to the rate of translation led to better empirical performance than did either the assumption that the gene expression level is roughly proportional to the protein level or the Bayesian model average of both assumptions. Availability: http://www.oisb.ca points to R code implementing the methods (R Development Core Team 2004). Contact: dbickel@uottawa.ca Supplementary information: http://www.davidbickel.com Oxford University Press 2009-03-15 2009-02-13 /pmc/articles/PMC2654806/ /pubmed/19218351 http://dx.doi.org/10.1093/bioinformatics/btp028 Text en © 2009 The Author(s) http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Papers
Bickel, David R.
Montazeri, Zahra
Hsieh, Pei-Chun
Beatty, Mary
Lawit, Shai J.
Bate, Nicholas J.
Gene network reconstruction from transcriptional dynamics under kinetic model uncertainty: a case for the second derivative
title Gene network reconstruction from transcriptional dynamics under kinetic model uncertainty: a case for the second derivative
title_full Gene network reconstruction from transcriptional dynamics under kinetic model uncertainty: a case for the second derivative
title_fullStr Gene network reconstruction from transcriptional dynamics under kinetic model uncertainty: a case for the second derivative
title_full_unstemmed Gene network reconstruction from transcriptional dynamics under kinetic model uncertainty: a case for the second derivative
title_short Gene network reconstruction from transcriptional dynamics under kinetic model uncertainty: a case for the second derivative
title_sort gene network reconstruction from transcriptional dynamics under kinetic model uncertainty: a case for the second derivative
topic Original Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2654806/
https://www.ncbi.nlm.nih.gov/pubmed/19218351
http://dx.doi.org/10.1093/bioinformatics/btp028
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