2012
DOI: 10.1021/sb300082b
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Dynamic Modeling of Cellular Populations within iBioSim

Abstract: As the complexity of synthetic genetic circuits increases, modeling is becoming a necessary first step to inform subsequent experimental efforts. In recent years, the design automation community has developed a wealth of computational tools for assisting experimentalists in designing and analyzing new genetic circuits at several scales. However, existing software primarily caters to either the DNA- or single-cell level, with little support for the multicellular level. To address this need, the iBioSim software… Show more

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Cited by 15 publications
(22 citation statements)
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“…We used our device to design two sets of 16 plasmids: one set of plasmids for Golden Gate and Gibson assembly, which contains a p15A origin of replication gene and kanamycin selection marker for bacteria, and one set of plasmids for yeast assembly, which contains both a 2 micron origin of replication gene with a tryptophan selection marker for yeast and an F1 origin of replication gene with an ampicillin selection marker for bacteria. Both sets of plasmids have two common sets of DNA inserts: four promoter (Prom) variants (1,2,9,11) and four bicistronic design (BCD) variants (1,2,20,21) coupled with a gf p gene. Prior to DNA assembly, these fragments for each assembly method are digested with DpnI (as well as BsaI for Golden Gate assembly) and gel purified (Figure 3a−c).…”
Section: ■ Results and Discussionmentioning
confidence: 99%
“…We used our device to design two sets of 16 plasmids: one set of plasmids for Golden Gate and Gibson assembly, which contains a p15A origin of replication gene and kanamycin selection marker for bacteria, and one set of plasmids for yeast assembly, which contains both a 2 micron origin of replication gene with a tryptophan selection marker for yeast and an F1 origin of replication gene with an ampicillin selection marker for bacteria. Both sets of plasmids have two common sets of DNA inserts: four promoter (Prom) variants (1,2,9,11) and four bicistronic design (BCD) variants (1,2,20,21) coupled with a gf p gene. Prior to DNA assembly, these fragments for each assembly method are digested with DpnI (as well as BsaI for Golden Gate assembly) and gel purified (Figure 3a−c).…”
Section: ■ Results and Discussionmentioning
confidence: 99%
“…When combined with high-fidelity genomic engineering 86,87 , higher efficiency transformation 88 , high-throughput phenotyping platforms 89 and improved in silico tools for pathway design and testing 9094 , the scale of reasonable plant engineering projects expands dramatically. Detailed knowledge of a genome, specifically the genotype-to-phenotype map, is essential for targeting and rapidly prototyping the optimal candidates for engineering.…”
Section: Perspectivementioning
confidence: 99%
“…In particular, simulation software programs should be expanded to support the Arrays, Distributions, Flux Balance Constraints, Hierarchical Model Composition, and Multistate and Multicomponent Species SBML packages. Several simulation software programs, including BioUML [25] and iBioSim [26], have already begun to support these packages. Unfortunately, most simulation software developers have insufficient funding to implement every package.…”
Section: Towards a Platform For Reproducible Modelingmentioning
confidence: 99%