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Titlebook: Computational Methods in Systems Biology; 10th International C David Gilbert,Monika Heiner Conference proceedings 2012 Springer-Verlag Berl

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书目名称Computational Methods in Systems Biology
副标题10th International C
编辑David Gilbert,Monika Heiner
视频video
概述Fast conference proceedings.State-of-the-art report.Up to date results
丛书名称Lecture Notes in Computer Science
图书封面Titlebook: Computational Methods in Systems Biology; 10th International C David Gilbert,Monika Heiner Conference proceedings 2012 Springer-Verlag Berl
描述This book constitutes the thoroughly refereed conference proceedings of the 10th International Conference on Computational Methods in Systems Biology, CMSB 2012, held in London, UK, during October 3-5, 2012. The 17 revised full papers and 8 flash posters presented together with the summaries of 3 invited papers were carefully reviewed and selected from 62 submissions. The papers cover the analysis of biological systems, networks, and data ranging from intercellular to multiscale. Topics included high-performance computing, and for the first time papers on synthetic biology.
出版日期Conference proceedings 2012
关键词Petri nets; cellular systems; gene networks; model checking; population dynamics
版次1
doihttps://doi.org/10.1007/978-3-642-33636-2
isbn_softcover978-3-642-33635-5
isbn_ebook978-3-642-33636-2Series ISSN 0302-9743 Series E-ISSN 1611-3349
issn_series 0302-9743
copyrightSpringer-Verlag Berlin Heidelberg 2012
The information of publication is updating

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Doing Research with Undergraduatesn be quantified using non-invasive imaging methods, histology is still the modality that provides the best combination of resolution and identification of cellular/sub-cellular substrate identities. The main limitation of histology is that it does not provide inherently consistent three-dimensional
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https://doi.org/10.1007/978-3-031-06645-0sses, namely Discrete Event Stochastic Processes (DESPs). Here we demonstrate the potential of HASL based verification in the context of genetic circuits. To this aim we consider the analysis of a model of gene expression with delayed stochastic dynamics, a class of systems whose dynamics includes b
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Aaron M. Ellison,Manisha V. Patelctable. Deterministic methods, while computationally more efficient, may fail to contribute reliable approximations for those models. In this paper, we suggest a reduction for models of cell-to-cell communication, based on symmetries of the underlying reaction network. To carry out a stochastic anal
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Aaron M. Ellison,Manisha V. Patels to understand the underlying mechanism of interaction. In this study we explore the disjoint and overlapping community structure of an integrated network for a major fungal pathogen of many cereal crops, .. The network was generated by combining sequence, protein interaction and co-expression data
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https://doi.org/10.1007/978-3-031-06641-2 of the growth rate of the cells during the exponential phase. This model is a piecewise non-linear system with two variables (the concentrations of two gene products) and an input (an inducer). We study the qualitative dynamics of the model and the bifurcation diagram with respect to the input. Mor
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Aaron M. Ellison,Manisha V. Patelh the optimal genetic manipulations, in terms of knockout, which also guarantee the growth of the organism. We introduce a multi-objective optimisation algorithm, called Genetic Design through Multi-Objective (GDMO), and test it in several organisms to maximise the production of key intermediate met
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