High-throughput generation, optimization and analysis of genome-scale metabolic models
Reconstructing a metabolic model from the genome sequence of an organism is a useful but arduous approach for predicting phenotypes. Henry et al . describe a resource that automates most of this process and apply it to create >100 new metabolic models of microbes. Genome-scale metabolic models ha...
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creator | Henry, Christopher S DeJongh, Matthew Best, Aaron A Frybarger, Paul M Linsay, Ben Stevens, Rick L |
description | Reconstructing a metabolic model from the genome sequence of an organism is a useful but arduous approach for predicting phenotypes. Henry
et al
. describe a resource that automates most of this process and apply it to create >100 new metabolic models of microbes.
Genome-scale metabolic models have proven to be valuable for predicting organism phenotypes from genotypes. Yet efforts to develop new models are failing to keep pace with genome sequencing. To address this problem, we introduce the Model SEED, a web-based resource for high-throughput generation, optimization and analysis of genome-scale metabolic models. The Model SEED integrates existing methods and introduces techniques to automate nearly every step of this process, taking ∼48 h to reconstruct a metabolic model from an assembled genome sequence. We apply this resource to generate 130 genome-scale metabolic models representing a taxonomically diverse set of bacteria. Twenty-two of the models were validated against available gene essentiality and Biolog data, with the average model accuracy determined to be 66% before optimization and 87% after optimization. |
doi_str_mv | 10.1038/nbt.1672 |
format | Article |
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et al
. describe a resource that automates most of this process and apply it to create >100 new metabolic models of microbes.
Genome-scale metabolic models have proven to be valuable for predicting organism phenotypes from genotypes. Yet efforts to develop new models are failing to keep pace with genome sequencing. To address this problem, we introduce the Model SEED, a web-based resource for high-throughput generation, optimization and analysis of genome-scale metabolic models. The Model SEED integrates existing methods and introduces techniques to automate nearly every step of this process, taking ∼48 h to reconstruct a metabolic model from an assembled genome sequence. We apply this resource to generate 130 genome-scale metabolic models representing a taxonomically diverse set of bacteria. Twenty-two of the models were validated against available gene essentiality and Biolog data, with the average model accuracy determined to be 66% before optimization and 87% after optimization.</description><identifier>ISSN: 1087-0156</identifier><identifier>EISSN: 1546-1696</identifier><identifier>DOI: 10.1038/nbt.1672</identifier><identifier>PMID: 20802497</identifier><language>eng</language><publisher>New York: Nature Publishing Group US</publisher><subject>631/114 ; 631/1647/1513 ; 631/326/41 ; 631/61/320 ; ACCURACY ; Agriculture ; BACTERIA ; Bacteria - classification ; Bacteria - genetics ; Bacteria - metabolism ; BASIC BIOLOGICAL SCIENCES ; Bioinformatics ; Biomedical and Life Sciences ; Biomedical Engineering/Biotechnology ; Biomedicine ; Biotechnology ; DNA sequencing ; GENERAL AND MISCELLANEOUS//MATHEMATICS, COMPUTING, AND INFORMATION SCIENCE ; GENES ; Genes, Bacterial ; Genetic aspects ; Genome, Bacterial - genetics ; Genomes ; Genomics ; Genotype & phenotype ; Genotypes ; Identification and classification ; Life Sciences ; Metabolism ; Methods ; Models, Biological ; Nucleotide sequencing ; OPTIMIZATION ; Phenotype ; resource ; SEEDS</subject><ispartof>Nat. Biotech, 2010-09, Vol.28 (9), p.977-982</ispartof><rights>Springer Nature America, Inc. 2010</rights><rights>COPYRIGHT 2010 Nature Publishing Group</rights><rights>Copyright Nature Publishing Group Sep 2010</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c608t-f2773cab8b4975cdc750f13577f94ee26a1c640270bbbd1f04173ad1e85e526c3</citedby><cites>FETCH-LOGICAL-c608t-f2773cab8b4975cdc750f13577f94ee26a1c640270bbbd1f04173ad1e85e526c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/nbt.1672$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/nbt.1672$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,881,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20802497$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/biblio/1018898$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Henry, Christopher S</creatorcontrib><creatorcontrib>DeJongh, Matthew</creatorcontrib><creatorcontrib>Best, Aaron A</creatorcontrib><creatorcontrib>Frybarger, Paul M</creatorcontrib><creatorcontrib>Linsay, Ben</creatorcontrib><creatorcontrib>Stevens, Rick L</creatorcontrib><creatorcontrib>Argonne National Lab. (ANL), Argonne, IL (United States)</creatorcontrib><title>High-throughput generation, optimization and analysis of genome-scale metabolic models</title><title>Nat. Biotech</title><addtitle>Nat Biotechnol</addtitle><addtitle>Nat Biotechnol</addtitle><description>Reconstructing a metabolic model from the genome sequence of an organism is a useful but arduous approach for predicting phenotypes. Henry
et al
. describe a resource that automates most of this process and apply it to create >100 new metabolic models of microbes.
Genome-scale metabolic models have proven to be valuable for predicting organism phenotypes from genotypes. Yet efforts to develop new models are failing to keep pace with genome sequencing. To address this problem, we introduce the Model SEED, a web-based resource for high-throughput generation, optimization and analysis of genome-scale metabolic models. The Model SEED integrates existing methods and introduces techniques to automate nearly every step of this process, taking ∼48 h to reconstruct a metabolic model from an assembled genome sequence. We apply this resource to generate 130 genome-scale metabolic models representing a taxonomically diverse set of bacteria. Twenty-two of the models were validated against available gene essentiality and Biolog data, with the average model accuracy determined to be 66% before optimization and 87% after optimization.</description><subject>631/114</subject><subject>631/1647/1513</subject><subject>631/326/41</subject><subject>631/61/320</subject><subject>ACCURACY</subject><subject>Agriculture</subject><subject>BACTERIA</subject><subject>Bacteria - classification</subject><subject>Bacteria - genetics</subject><subject>Bacteria - metabolism</subject><subject>BASIC BIOLOGICAL SCIENCES</subject><subject>Bioinformatics</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedical Engineering/Biotechnology</subject><subject>Biomedicine</subject><subject>Biotechnology</subject><subject>DNA sequencing</subject><subject>GENERAL AND MISCELLANEOUS//MATHEMATICS, COMPUTING, AND INFORMATION SCIENCE</subject><subject>GENES</subject><subject>Genes, Bacterial</subject><subject>Genetic aspects</subject><subject>Genome, Bacterial - genetics</subject><subject>Genomes</subject><subject>Genomics</subject><subject>Genotype & phenotype</subject><subject>Genotypes</subject><subject>Identification and classification</subject><subject>Life Sciences</subject><subject>Metabolism</subject><subject>Methods</subject><subject>Models, Biological</subject><subject>Nucleotide sequencing</subject><subject>OPTIMIZATION</subject><subject>Phenotype</subject><subject>resource</subject><subject>SEEDS</subject><issn>1087-0156</issn><issn>1546-1696</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>N95</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqN0ltr1UAQAOAgir0o-Ask6EMVmuPuJtlNHktRWygUvPR12WwmOVuS7HFnA9Zf7xxTezzog4Tcv5nMTiZJXnC24iyv3k1NXHGpxKPkkJeFzLis5WO6ZpXKGC_lQXKEeMsYk4WUT5MDwSomilodJjcXrl9ncR383K83c0x7mCCY6Px0mvpNdKP78esuNVNLuxnu0GHquy30I2RozQDpCNE0fnA2HX0LAz5LnnRmQHh-fz5Ovn54_-X8Iru6_nh5fnaVWcmqmHVCqdyapmqomNK2VpWs43mpVFcXAEIabmXBhGJN07S8YwVXuWk5VCWUQtr8OHm15PUYnUbrIti19dMENmrOeFXVFaGTBW2C_zYDRj06tDAMZgI_o1YlfaKua7FL9yBv_Rxo0VvEBJNUCaHXC-pp5dpNnY_B2G1KfSZyJZkQsiC1-oeirYXRUYXQOXq-F_B2L4BMhO-xNzOivvz86f_t9c2-Pf3DNjO6CZAOSD8-4hKyx98s3AaPGKDTm-BGE-6onXo7bJqGTW-HjejL-27NzQjtA_w9XbsykV5NPYRdO_9K9hMybNjZ</recordid><startdate>20100901</startdate><enddate>20100901</enddate><creator>Henry, Christopher S</creator><creator>DeJongh, Matthew</creator><creator>Best, Aaron A</creator><creator>Frybarger, Paul M</creator><creator>Linsay, Ben</creator><creator>Stevens, Rick L</creator><general>Nature Publishing Group US</general><general>Nature Publishing Group</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>N95</scope><scope>XI7</scope><scope>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QO</scope><scope>7QP</scope><scope>7QR</scope><scope>7T7</scope><scope>7TK</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M2P</scope><scope>M7P</scope><scope>M7S</scope><scope>MBDVC</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PTHSS</scope><scope>Q9U</scope><scope>RC3</scope><scope>7X8</scope><scope>OTOTI</scope></search><sort><creationdate>20100901</creationdate><title>High-throughput generation, optimization and analysis of genome-scale metabolic models</title><author>Henry, Christopher S ; 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Biotech</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Henry, Christopher S</au><au>DeJongh, Matthew</au><au>Best, Aaron A</au><au>Frybarger, Paul M</au><au>Linsay, Ben</au><au>Stevens, Rick L</au><aucorp>Argonne National Lab. (ANL), Argonne, IL (United States)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>High-throughput generation, optimization and analysis of genome-scale metabolic models</atitle><jtitle>Nat. Biotech</jtitle><stitle>Nat Biotechnol</stitle><addtitle>Nat Biotechnol</addtitle><date>2010-09-01</date><risdate>2010</risdate><volume>28</volume><issue>9</issue><spage>977</spage><epage>982</epage><pages>977-982</pages><issn>1087-0156</issn><eissn>1546-1696</eissn><abstract>Reconstructing a metabolic model from the genome sequence of an organism is a useful but arduous approach for predicting phenotypes. Henry
et al
. describe a resource that automates most of this process and apply it to create >100 new metabolic models of microbes.
Genome-scale metabolic models have proven to be valuable for predicting organism phenotypes from genotypes. Yet efforts to develop new models are failing to keep pace with genome sequencing. To address this problem, we introduce the Model SEED, a web-based resource for high-throughput generation, optimization and analysis of genome-scale metabolic models. The Model SEED integrates existing methods and introduces techniques to automate nearly every step of this process, taking ∼48 h to reconstruct a metabolic model from an assembled genome sequence. We apply this resource to generate 130 genome-scale metabolic models representing a taxonomically diverse set of bacteria. Twenty-two of the models were validated against available gene essentiality and Biolog data, with the average model accuracy determined to be 66% before optimization and 87% after optimization.</abstract><cop>New York</cop><pub>Nature Publishing Group US</pub><pmid>20802497</pmid><doi>10.1038/nbt.1672</doi><tpages>6</tpages></addata></record> |
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subjects | 631/114 631/1647/1513 631/326/41 631/61/320 ACCURACY Agriculture BACTERIA Bacteria - classification Bacteria - genetics Bacteria - metabolism BASIC BIOLOGICAL SCIENCES Bioinformatics Biomedical and Life Sciences Biomedical Engineering/Biotechnology Biomedicine Biotechnology DNA sequencing GENERAL AND MISCELLANEOUS//MATHEMATICS, COMPUTING, AND INFORMATION SCIENCE GENES Genes, Bacterial Genetic aspects Genome, Bacterial - genetics Genomes Genomics Genotype & phenotype Genotypes Identification and classification Life Sciences Metabolism Methods Models, Biological Nucleotide sequencing OPTIMIZATION Phenotype resource SEEDS |
title | High-throughput generation, optimization and analysis of genome-scale metabolic models |
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