A cis-regulatory logic simulator

<p>Abstract</p> <p>Background</p> <p>A major goal of computational studies of gene regulation is to accurately predict the expression of genes based on the cis-regulatory content of their promoters. The development of computational methods to decode the interactions amo...

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Main Authors: Cohen Barak A, Gertz Jason, Zeigler Robert D
Format: Article
Language:English
Published: BMC 2007-07-01
Series:BMC Bioinformatics
Online Access:http://www.biomedcentral.com/1471-2105/8/272
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spelling doaj-6a8a6dd354724a5d99d1167247236dc42020-11-25T00:20:32ZengBMCBMC Bioinformatics1471-21052007-07-018127210.1186/1471-2105-8-272A cis-regulatory logic simulatorCohen Barak AGertz JasonZeigler Robert D<p>Abstract</p> <p>Background</p> <p>A major goal of computational studies of gene regulation is to accurately predict the expression of genes based on the cis-regulatory content of their promoters. The development of computational methods to decode the interactions among cis-regulatory elements has been slow, in part, because it is difficult to know, without extensive experimental validation, whether a particular method identifies the correct cis-regulatory interactions that underlie a given set of expression data. There is an urgent need for test expression data in which the interactions among cis-regulatory sites that produce the data are known. The ability to rapidly generate such data sets would facilitate the development and comparison of computational methods that predict gene expression patterns from promoter sequence.</p> <p>Results</p> <p>We developed a gene expression simulator which generates expression data using user-defined interactions between cis-regulatory sites. The simulator can incorporate additive, cooperative, competitive, and synergistic interactions between regulatory elements. Constraints on the spacing, distance, and orientation of regulatory elements and their interactions may also be defined and Gaussian noise can be added to the expression values. The simulator allows for a data transformation that simulates the sigmoid shape of expression levels from real promoters. We found good agreement between sets of simulated promoters and predicted regulatory modules from real expression data. We present several data sets that may be useful for testing new methodologies for predicting gene expression from promoter sequence.</p> <p>Conclusion</p> <p>We developed a flexible gene expression simulator that rapidly generates large numbers of simulated promoters and their corresponding transcriptional output based on specified interactions between cis-regulatory sites. When appropriate rule sets are used, the data generated by our simulator faithfully reproduces experimentally derived data sets. We anticipate that using simulated gene expression data sets will facilitate the direct comparison of computational strategies to predict gene expression from promoter sequence. The source code is available online and as additional material. The test sets are available as additional material.</p> http://www.biomedcentral.com/1471-2105/8/272
collection DOAJ
language English
format Article
sources DOAJ
author Cohen Barak A
Gertz Jason
Zeigler Robert D
spellingShingle Cohen Barak A
Gertz Jason
Zeigler Robert D
A cis-regulatory logic simulator
BMC Bioinformatics
author_facet Cohen Barak A
Gertz Jason
Zeigler Robert D
author_sort Cohen Barak A
title A cis-regulatory logic simulator
title_short A cis-regulatory logic simulator
title_full A cis-regulatory logic simulator
title_fullStr A cis-regulatory logic simulator
title_full_unstemmed A cis-regulatory logic simulator
title_sort cis-regulatory logic simulator
publisher BMC
series BMC Bioinformatics
issn 1471-2105
publishDate 2007-07-01
description <p>Abstract</p> <p>Background</p> <p>A major goal of computational studies of gene regulation is to accurately predict the expression of genes based on the cis-regulatory content of their promoters. The development of computational methods to decode the interactions among cis-regulatory elements has been slow, in part, because it is difficult to know, without extensive experimental validation, whether a particular method identifies the correct cis-regulatory interactions that underlie a given set of expression data. There is an urgent need for test expression data in which the interactions among cis-regulatory sites that produce the data are known. The ability to rapidly generate such data sets would facilitate the development and comparison of computational methods that predict gene expression patterns from promoter sequence.</p> <p>Results</p> <p>We developed a gene expression simulator which generates expression data using user-defined interactions between cis-regulatory sites. The simulator can incorporate additive, cooperative, competitive, and synergistic interactions between regulatory elements. Constraints on the spacing, distance, and orientation of regulatory elements and their interactions may also be defined and Gaussian noise can be added to the expression values. The simulator allows for a data transformation that simulates the sigmoid shape of expression levels from real promoters. We found good agreement between sets of simulated promoters and predicted regulatory modules from real expression data. We present several data sets that may be useful for testing new methodologies for predicting gene expression from promoter sequence.</p> <p>Conclusion</p> <p>We developed a flexible gene expression simulator that rapidly generates large numbers of simulated promoters and their corresponding transcriptional output based on specified interactions between cis-regulatory sites. When appropriate rule sets are used, the data generated by our simulator faithfully reproduces experimentally derived data sets. We anticipate that using simulated gene expression data sets will facilitate the direct comparison of computational strategies to predict gene expression from promoter sequence. The source code is available online and as additional material. The test sets are available as additional material.</p>
url http://www.biomedcentral.com/1471-2105/8/272
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