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Accelerated discovery via a whole-cell model
Whole-cell modeling promises to facilitate scientific inquiry by prioritizing future experiments based on existing datasets. To test this promise, we compared simulated growth rates with new measurements for all viable single-gene disruption strains in Mycoplasma genitalium. The discrepancies betwee...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3856890/ https://www.ncbi.nlm.nih.gov/pubmed/24185838 http://dx.doi.org/10.1038/nmeth.2724 |
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author | Sanghvi, Jayodita C. Regot, Sergi Carrasco, Silvia Karr, Jonathan R. Gutschow, Miriam V. Bolival, Benjamin Covert, Markus W. |
author_facet | Sanghvi, Jayodita C. Regot, Sergi Carrasco, Silvia Karr, Jonathan R. Gutschow, Miriam V. Bolival, Benjamin Covert, Markus W. |
author_sort | Sanghvi, Jayodita C. |
collection | PubMed |
description | Whole-cell modeling promises to facilitate scientific inquiry by prioritizing future experiments based on existing datasets. To test this promise, we compared simulated growth rates with new measurements for all viable single-gene disruption strains in Mycoplasma genitalium. The discrepancies between simulations and experiments led to novel model predictions about specific kinetic parameters that we subsequently validated. These findings represent the first application of whole-cell modeling to accelerate biological discovery. |
format | Online Article Text |
id | pubmed-3856890 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
record_format | MEDLINE/PubMed |
spelling | pubmed-38568902014-06-01 Accelerated discovery via a whole-cell model Sanghvi, Jayodita C. Regot, Sergi Carrasco, Silvia Karr, Jonathan R. Gutschow, Miriam V. Bolival, Benjamin Covert, Markus W. Nat Methods Article Whole-cell modeling promises to facilitate scientific inquiry by prioritizing future experiments based on existing datasets. To test this promise, we compared simulated growth rates with new measurements for all viable single-gene disruption strains in Mycoplasma genitalium. The discrepancies between simulations and experiments led to novel model predictions about specific kinetic parameters that we subsequently validated. These findings represent the first application of whole-cell modeling to accelerate biological discovery. 2013-11-03 2013-12 /pmc/articles/PMC3856890/ /pubmed/24185838 http://dx.doi.org/10.1038/nmeth.2724 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Sanghvi, Jayodita C. Regot, Sergi Carrasco, Silvia Karr, Jonathan R. Gutschow, Miriam V. Bolival, Benjamin Covert, Markus W. Accelerated discovery via a whole-cell model |
title | Accelerated discovery via a whole-cell model |
title_full | Accelerated discovery via a whole-cell model |
title_fullStr | Accelerated discovery via a whole-cell model |
title_full_unstemmed | Accelerated discovery via a whole-cell model |
title_short | Accelerated discovery via a whole-cell model |
title_sort | accelerated discovery via a whole-cell model |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3856890/ https://www.ncbi.nlm.nih.gov/pubmed/24185838 http://dx.doi.org/10.1038/nmeth.2724 |
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