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Applying dynamic Bayesian networks to perturbed gene expression data
A central goal of molecular biology is to understand the regulatory mechanisms of gene transcription and protein synthesis. Because of their solid basis in statistics, allowing to deal with the stochastic aspects of gene expressions and noisy measurements in a natural way, Bayesian networks appear a...
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Published in: | BMC bioinformatics 2006-05, Vol.7 (1), p.249-249, Article 249 |
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description | A central goal of molecular biology is to understand the regulatory mechanisms of gene transcription and protein synthesis. Because of their solid basis in statistics, allowing to deal with the stochastic aspects of gene expressions and noisy measurements in a natural way, Bayesian networks appear attractive in the field of inferring gene interactions structure from microarray experiments data. However, the basic formalism has some disadvantages, e.g. it is sometimes hard to distinguish between the origin and the target of an interaction. Two kinds of microarray experiments yield data particularly rich in information regarding the direction of interactions: time series and perturbation experiments. In order to correctly handle them, the basic formalism must be modified. For example, dynamic Bayesian networks (DBN) apply to time series microarray data. To our knowledge the DBN technique has not been applied in the context of perturbation experiments.
We extend the framework of dynamic Bayesian networks in order to incorporate perturbations. Moreover, an exact algorithm for inferring an optimal network is proposed and a discretization method specialized for time series data from perturbation experiments is introduced. We apply our procedure to realistic simulations data. The results are compared with those obtained by standard DBN learning techniques. Moreover, the advantages of using exact learning algorithm instead of heuristic methods are analyzed.
We show that the quality of inferred networks dramatically improves when using data from perturbation experiments. We also conclude that the exact algorithm should be used when it is possible, i.e. when considered set of genes is small enough. |
doi_str_mv | 10.1186/1471-2105-7-249 |
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We extend the framework of dynamic Bayesian networks in order to incorporate perturbations. Moreover, an exact algorithm for inferring an optimal network is proposed and a discretization method specialized for time series data from perturbation experiments is introduced. We apply our procedure to realistic simulations data. The results are compared with those obtained by standard DBN learning techniques. Moreover, the advantages of using exact learning algorithm instead of heuristic methods are analyzed.
We show that the quality of inferred networks dramatically improves when using data from perturbation experiments. We also conclude that the exact algorithm should be used when it is possible, i.e. when considered set of genes is small enough.</description><identifier>ISSN: 1471-2105</identifier><identifier>EISSN: 1471-2105</identifier><identifier>DOI: 10.1186/1471-2105-7-249</identifier><identifier>PMID: 16681847</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Algorithms ; Artificial Intelligence ; Bayes Theorem ; Computer Simulation ; Gene Expression - physiology ; Gene Expression Profiling - methods ; Methodology ; Models, Biological ; Models, Statistical ; Oligonucleotide Array Sequence Analysis - methods ; Pattern Recognition, Automated - methods ; Proteome - metabolism ; Signal Transduction - physiology</subject><ispartof>BMC bioinformatics, 2006-05, Vol.7 (1), p.249-249, Article 249</ispartof><rights>Copyright © 2006 Dojer et al; licensee BioMed Central Ltd. 2006 Dojer et al; licensee BioMed Central Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b578t-c3819c67b87810a6f210c53e40e0334dc3fb4bc4bef9d4aca445135f0001aeef3</citedby><cites>FETCH-LOGICAL-b578t-c3819c67b87810a6f210c53e40e0334dc3fb4bc4bef9d4aca445135f0001aeef3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1513402/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1513402/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16681847$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dojer, Norbert</creatorcontrib><creatorcontrib>Gambin, Anna</creatorcontrib><creatorcontrib>Mizera, Andrzej</creatorcontrib><creatorcontrib>Wilczyński, Bartek</creatorcontrib><creatorcontrib>Tiuryn, Jerzy</creatorcontrib><title>Applying dynamic Bayesian networks to perturbed gene expression data</title><title>BMC bioinformatics</title><addtitle>BMC Bioinformatics</addtitle><description>A central goal of molecular biology is to understand the regulatory mechanisms of gene transcription and protein synthesis. Because of their solid basis in statistics, allowing to deal with the stochastic aspects of gene expressions and noisy measurements in a natural way, Bayesian networks appear attractive in the field of inferring gene interactions structure from microarray experiments data. However, the basic formalism has some disadvantages, e.g. it is sometimes hard to distinguish between the origin and the target of an interaction. Two kinds of microarray experiments yield data particularly rich in information regarding the direction of interactions: time series and perturbation experiments. In order to correctly handle them, the basic formalism must be modified. For example, dynamic Bayesian networks (DBN) apply to time series microarray data. To our knowledge the DBN technique has not been applied in the context of perturbation experiments.
We extend the framework of dynamic Bayesian networks in order to incorporate perturbations. Moreover, an exact algorithm for inferring an optimal network is proposed and a discretization method specialized for time series data from perturbation experiments is introduced. We apply our procedure to realistic simulations data. The results are compared with those obtained by standard DBN learning techniques. Moreover, the advantages of using exact learning algorithm instead of heuristic methods are analyzed.
We show that the quality of inferred networks dramatically improves when using data from perturbation experiments. We also conclude that the exact algorithm should be used when it is possible, i.e. when considered set of genes is small enough.</description><subject>Algorithms</subject><subject>Artificial Intelligence</subject><subject>Bayes Theorem</subject><subject>Computer Simulation</subject><subject>Gene Expression - physiology</subject><subject>Gene Expression Profiling - methods</subject><subject>Methodology</subject><subject>Models, Biological</subject><subject>Models, Statistical</subject><subject>Oligonucleotide Array Sequence Analysis - methods</subject><subject>Pattern Recognition, Automated - methods</subject><subject>Proteome - metabolism</subject><subject>Signal Transduction - physiology</subject><issn>1471-2105</issn><issn>1471-2105</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNqFkk1v1DAQhi0EoqVw5oZy4hZqx5-5ILWlhUqVuMDZGjvjxSWJg50t7L8ny65KVwL1ZGvm1aNHM0PIa0bfMWbUKROa1Q2jstZ1I9on5Pi-8vTB_4i8KOWWUqYNlc_JEVPKMCP0MflwNk39Jo6rqtuMMERfncMGS4SxGnH-mfL3Us2pmjDP6-ywq1Y4YoW_poylxDRWHczwkjwL0Bd8tX9PyNeryy8Xn-qbzx-vL85uaie1mWvPDWu90s5owyiosKh5yVFQpJyLzvPghPPCYWg7AR6EkIzLQBdxQAz8hFzvuF2CWzvlOEDe2ATR_imkvLKQ5-h7tEAbBN8xp00rGhrAyxZbHlC1ygHCwnq_Y01rN2DncZwz9AfQw84Yv9lVurNscRK0WQDnO4CL6T-Aw45Pg91uxG43YrVd9rVA3u4tcvqxxjLbIRaPfQ8jpnWxyigptdKPBhvWCNYY9WiQtUJxqbb-p7ugz6mUjOFenVG7Pa5_yL55OLK_-f018d8Mbsvq</recordid><startdate>20060508</startdate><enddate>20060508</enddate><creator>Dojer, Norbert</creator><creator>Gambin, Anna</creator><creator>Mizera, Andrzej</creator><creator>Wilczyński, Bartek</creator><creator>Tiuryn, Jerzy</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><general>BMC</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20060508</creationdate><title>Applying dynamic Bayesian networks to perturbed gene expression data</title><author>Dojer, Norbert ; Gambin, Anna ; Mizera, Andrzej ; Wilczyński, Bartek ; Tiuryn, Jerzy</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b578t-c3819c67b87810a6f210c53e40e0334dc3fb4bc4bef9d4aca445135f0001aeef3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Algorithms</topic><topic>Artificial Intelligence</topic><topic>Bayes Theorem</topic><topic>Computer Simulation</topic><topic>Gene Expression - physiology</topic><topic>Gene Expression Profiling - methods</topic><topic>Methodology</topic><topic>Models, Biological</topic><topic>Models, Statistical</topic><topic>Oligonucleotide Array Sequence Analysis - methods</topic><topic>Pattern Recognition, Automated - methods</topic><topic>Proteome - metabolism</topic><topic>Signal Transduction - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dojer, Norbert</creatorcontrib><creatorcontrib>Gambin, Anna</creatorcontrib><creatorcontrib>Mizera, Andrzej</creatorcontrib><creatorcontrib>Wilczyński, Bartek</creatorcontrib><creatorcontrib>Tiuryn, Jerzy</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>BMC bioinformatics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dojer, Norbert</au><au>Gambin, Anna</au><au>Mizera, Andrzej</au><au>Wilczyński, Bartek</au><au>Tiuryn, Jerzy</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Applying dynamic Bayesian networks to perturbed gene expression data</atitle><jtitle>BMC bioinformatics</jtitle><addtitle>BMC Bioinformatics</addtitle><date>2006-05-08</date><risdate>2006</risdate><volume>7</volume><issue>1</issue><spage>249</spage><epage>249</epage><pages>249-249</pages><artnum>249</artnum><issn>1471-2105</issn><eissn>1471-2105</eissn><abstract>A central goal of molecular biology is to understand the regulatory mechanisms of gene transcription and protein synthesis. Because of their solid basis in statistics, allowing to deal with the stochastic aspects of gene expressions and noisy measurements in a natural way, Bayesian networks appear attractive in the field of inferring gene interactions structure from microarray experiments data. However, the basic formalism has some disadvantages, e.g. it is sometimes hard to distinguish between the origin and the target of an interaction. Two kinds of microarray experiments yield data particularly rich in information regarding the direction of interactions: time series and perturbation experiments. In order to correctly handle them, the basic formalism must be modified. For example, dynamic Bayesian networks (DBN) apply to time series microarray data. To our knowledge the DBN technique has not been applied in the context of perturbation experiments.
We extend the framework of dynamic Bayesian networks in order to incorporate perturbations. Moreover, an exact algorithm for inferring an optimal network is proposed and a discretization method specialized for time series data from perturbation experiments is introduced. We apply our procedure to realistic simulations data. The results are compared with those obtained by standard DBN learning techniques. Moreover, the advantages of using exact learning algorithm instead of heuristic methods are analyzed.
We show that the quality of inferred networks dramatically improves when using data from perturbation experiments. We also conclude that the exact algorithm should be used when it is possible, i.e. when considered set of genes is small enough.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>16681847</pmid><doi>10.1186/1471-2105-7-249</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Algorithms Artificial Intelligence Bayes Theorem Computer Simulation Gene Expression - physiology Gene Expression Profiling - methods Methodology Models, Biological Models, Statistical Oligonucleotide Array Sequence Analysis - methods Pattern Recognition, Automated - methods Proteome - metabolism Signal Transduction - physiology |
title | Applying dynamic Bayesian networks to perturbed gene expression data |
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