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1.
Artigo em Inglês | MEDLINE | ID: mdl-17048401

RESUMO

Converting a biochemical reaction network to a set of kinetic rate equations is tedious and error prone. We describe known interface paradigms for inputing models of intracellular regulatory networks: graphical layout (diagrams), wizards, scripting languages, and direct entry of chemical equations. We present the JigCell Model Builder, which allows users to define models as a set of reaction equations using a spreadsheet (an example of direct entry of equations) and outputs model definitions in the Systems Biology Markup Language, Level 2. We present the results of two usability studies. The spreadsheet paradigm demonstrated its effectiveness in reducing the number of errors made by modelers when compared to hand conversion of a wiring diagram to differential equations. A comparison of representatives of the four interface paradigms for a simple model of the cell cycle was conducted which measured time, mouse clicks, and keystrokes to enter the model, and the number of screens needed to view the contents of the model. All four paradigms had similar data entry times. The spreadsheet and scripting language approaches require significantly fewer screens to view the models than do the wizard or graphical layout approaches.


Assuntos
Metabolismo/fisiologia , Modelos Biológicos , Biologia de Sistemas/métodos , Interface Usuário-Computador , Algoritmos , Simulação por Computador , Cinética
2.
OMICS ; 7(3): 285-99, 2003.
Artigo em Inglês | MEDLINE | ID: mdl-14583117

RESUMO

The life of a cell is governed by the physicochemical properties of a complex network of interacting macromolecules (primarily genes and proteins). Hence, a full scientific understanding of and rational engineering approach to cell physiology require accurate mathematical models of the spatial and temporal dynamics of these macromolecular assemblies, especially the networks involved in integrating signals and regulating cellular responses. The Virginia Tech Consortium is involved in three specific goals of DARPA's computational biology program (Bio-COMP): to create effective software tools for modeling gene-protein-metabolite networks, to employ these tools in creating a new generation of realistic models, and to test and refine these models by well-conceived experimental studies. The special emphasis of this group is to understand the mechanisms of cell cycle control in eukaryotes (yeast cells and frog eggs). The software tools developed at Virginia Tech are designed to meet general requirements of modeling regulatory networks and are collected in a problem-solving environment called JigCell.


Assuntos
Fenômenos Fisiológicos Celulares , Biologia Computacional/métodos , Modelos Biológicos , Software , Animais , Ciclo Celular/fisiologia , Proteínas de Ciclo Celular/metabolismo , Simulação por Computador , Regulação da Expressão Gênica , Regulação da Expressão Gênica no Desenvolvimento , Óvulo/citologia , Óvulo/metabolismo , Virginia , Leveduras/citologia , Leveduras/crescimento & desenvolvimento , Leveduras/metabolismo
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