<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Faraji M</submitter><funding>NIAID NIH HHS</funding><funding>NIEHS NIH HHS</funding><funding>National Institutes of Health</funding><funding>NIH HHS</funding><funding>National Science Foundation</funding><pagination>2165-2172</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5860468</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>33(14)</volume><pubmed_abstract>&lt;h4>Motivation&lt;/h4>Most metabolic pathways contain more reactions than metabolites and therefore have a wide stoichiometric matrix that corresponds to infinitely many possible flux distributions that are perfectly compatible with the dynamics of the metabolites in a given dataset. This under-determinedness poses a challenge for the quantitative characterization of flux distributions from time series data and thus for the design of adequate, predictive models. Here we propose a method that reduces the degrees of freedom in a stepwise manner and leads to a dynamic flux distribution that is, in a statistical sense, likely to be close to the true distribution.&lt;h4>Results&lt;/h4>We applied the proposed method to the lignin biosynthesis pathway in switchgrass. The system consists of 16 metabolites </pubmed_abstract><journal>Bioinformatics (Oxford, England)</journal><pubmed_title>Stepwise inference of likely dynamic flux distributions from metabolic time series data.</pubmed_title><pmcid>PMC5860468</pmcid><funding_grant_id>MCB-0958172, MCB-0946595 and MCB-1517588</funding_grant_id><funding_grant_id>DEB-1241046</funding_grant_id><funding_grant_id>HHSN272201200031C</funding_grant_id><funding_grant_id>P51 OD011132</funding_grant_id><funding_grant_id>MCB 1411672</funding_grant_id><funding_grant_id>P30 ES019776</funding_grant_id><pubmed_authors>Voit EO</pubmed_authors><pubmed_authors>Faraji M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Stepwise inference of likely dynamic flux distributions from metabolic time series data.</name><description>&lt;h4>Motivation&lt;/h4>Most metabolic pathways contain more reactions than metabolites and therefore have a wide stoichiometric matrix that corresponds to infinitely many possible flux distributions that are perfectly compatible with the dynamics of the metabolites in a given dataset. This under-determinedness poses a challenge for the quantitative characterization of flux distributions from time series data and thus for the design of adequate, predictive models. Here we propose a method that reduces the degrees of freedom in a stepwise manner and leads to a dynamic flux distribution that is, in a statistical sense, likely to be close to the true distribution.&lt;h4>Results&lt;/h4>We applied the proposed method to the lignin biosynthesis pathway in switchgrass. The system consists of 16 metabolites </description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Jul</publication><modification>2025-04-05T15:11:20.619Z</modification><creation>2019-03-26T23:46:22Z</creation></dates><accession>S-EPMC5860468</accession><cross_references><pubmed>28334199</pubmed><doi>10.1093/bioinformatics/btx126</doi></cross_references></HashMap>