<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Tourigny DS</submitter><funding>Life Sciences Research Foundation</funding><funding>National Institutes of Health</funding><funding>NIGMS NIH HHS</funding><funding>National Science Foundation</funding><pagination>5231-5242</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8715178</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>120(23)</volume><pubmed_abstract>Stochasticity from gene expression in single cells is known to drive metabolic heterogeneity at the level of cellular populations, which is understood to have important consequences for issues such as microbial drug tolerance and treatment of human diseases like cancer. Despite considerable advancements in profiling the genomes, transcriptomes, and proteomes of single cells, it remains difficult to experimentally characterize their metabolism at the genome scale. Computational methods could bridge this gap toward a systems understanding of single-cell biology. To address this challenge, we developed stochastic simulation algorithm with flux-balance analysis embedded (SSA-FBA), a computational framework for simulating the stochastic dynamics of the metabolism of individual cells using genom</pubmed_abstract><journal>Biophysical journal</journal><pubmed_title>Simulating single-cell metabolism using a stochastic flux-balance analysis algorithm.</pubmed_title><pmcid>PMC8715178</pmcid><funding_grant_id>1649014</funding_grant_id><funding_grant_id>R35GM119771</funding_grant_id><funding_grant_id>R35 GM119771</funding_grant_id><pubmed_authors>Karr JR</pubmed_authors><pubmed_authors>Tourigny DS</pubmed_authors><pubmed_authors>Goldberg AP</pubmed_authors></additional><is_claimable>false</is_claimable><name>Simulating single-cell metabolism using a stochastic flux-balance analysis algorithm.</name><description>Stochasticity from gene expression in single cells is known to drive metabolic heterogeneity at the level of cellular populations, which is understood to have important consequences for issues such as microbial drug tolerance and treatment of human diseases like cancer. Despite considerable advancements in profiling the genomes, transcriptomes, and proteomes of single cells, it remains difficult to experimentally characterize their metabolism at the genome scale. Computational methods could bridge this gap toward a systems understanding of single-cell biology. To address this challenge, we developed stochastic simulation algorithm with flux-balance analysis embedded (SSA-FBA), a computational framework for simulating the stochastic dynamics of the metabolism of individual cells using genom</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Dec</publication><modification>2025-04-04T23:44:43.975Z</modification><creation>2025-04-04T23:44:43.975Z</creation></dates><accession>S-EPMC8715178</accession><cross_references><pubmed>34757076</pubmed><doi>10.1016/j.bpj.2021.10.038</doi></cross_references></HashMap>