Modeling systems biology from the point of view of discrete and hybrid systems

Author(s):  
M. Antoniotti
2018 ◽  
Vol 43 (3) ◽  
pp. 219-243 ◽  
Author(s):  
Szymon Wasik

Abstract Crowdsourcing is a very effective technique for outsourcing work to a vast network usually comprising anonymous people. In this study, we review the application of crowdsourcing to modeling systems originating from systems biology. We consider a variety of verified approaches, including well-known projects such as EyeWire, FoldIt, and DREAM Challenges, as well as novel projects conducted at the European Center for Bioinformatics and Genomics. The latter projects utilized crowdsourced serious games to design models of dynamic biological systems, and it was demonstrated that these models could be used successfully to involve players without domain knowledge. We conclude the review of these systems by providing 10 guidelines to facilitate the efficient use of crowdsourcing.


2013 ◽  
pp. 1494-1521
Author(s):  
Jose M. Garcia-Manteiga

Metabolomics represents the new ‘omics’ approach of the functional genomics era. It consists in the identification and quantification of all small molecules, namely metabolites, in a given biological system. While metabolomics refers to the analysis of any possible biological system, metabonomics is specifically applied to disease and physiopathological situations. The data collected within these approaches is highly integrative of the other higher levels and is hence amenable to be explored with a top-down systems biology point of view. The aim of this chapter is to give a global view of the state of the art in metabolomics describing the two analytical techniques usually used to give rise to this kind of data, nuclear magnetic resonance, NMR, and mass spectrometry. In addition, the author will focus on the different data analysis tools that can be applied to such studies to extract information with special interest at the attempts to integrate metabolomics with other ‘omics’ approaches and its relevance in systems biology modeling.


Author(s):  
Jose M. Garcia-Manteiga

Metabolomics represents the new ‘omics’ approach of the functional genomics era. It consists in the identification and quantification of all small molecules, namely metabolites, in a given biological system. While metabolomics refers to the analysis of any possible biological system, metabonomics is specifically applied to disease and physiopathological situations. The data collected within these approaches is highly integrative of the other higher levels and is hence amenable to be explored with a top-down systems biology point of view. The aim of this chapter is to give a global view of the state of the art in metabolomics describing the two analytical techniques usually used to give rise to this kind of data, nuclear magnetic resonance, NMR, and mass spectrometry. In addition, the author will focus on the different data analysis tools that can be applied to such studies to extract information with special interest at the attempts to integrate metabolomics with other ‘omics’ approaches and its relevance in systems biology modeling.


Author(s):  
Amit Chattopadhyay

This chapter reviews the principles of systems biology and their application through computational methods (bioinformatics, computational biomodeling, genomics, proteomics, oral human microbiome, molecular modeling, systems biology, protein structure prediction, structural genomics, computational biochemistry and computational biophysics methods and projects) that have been applied to oral diseases research. The emphasis of the chapter is on concepts from molecular biology, genetics, and traditional pathology to provide new insights into oral diseases, and the associated technologies to provide new diagnostic, therapeutic and prognostic information. Another goal of the manuscript will be to serve as a central reference to access of information about systems biology resources for research into oral diseases.


2012 ◽  
Vol 11 ◽  
pp. CIN.S8185 ◽  
Author(s):  
Xiangfang Li ◽  
Lijun Qian ◽  
Michale L. Bittner ◽  
Edward R. Dougherty

Motivated by the frustration of translation of research advances in the molecular and cellular biology of cancer into treatment, this study calls for cross-disciplinary efforts and proposes a methodology of incorporating drug pharmacology information into drug therapeutic response modeling using a computational systems biology approach. The objectives are two fold. The first one is to involve effective mathematical modeling in the drug development stage to incorporate preclinical and clinical data in order to decrease costs of drug development and increase pipeline productivity, since it is extremely expensive and difficult to get the optimal compromise of dosage and schedule through empirical testing. The second objective is to provide valuable suggestions to adjust individual drug dosing regimens to improve therapeutic effects considering most anticancer agents have wide inter-individual pharmacokinetic variability and a narrow therapeutic index. A dynamic hybrid systems model is proposed to study drug antitumor effect from the perspective of tumor growth dynamics, specifically the dosing and schedule of the periodic drug intake, and a drug's pharmacokinetics and pharmacodynamics information are linked together in the proposed model using a state-space approach. It is proved analytically that there exists an optimal drug dosage and interval administration point, and demonstrated through simulation study.


Author(s):  
A. Franzoni ◽  
L. Magistri ◽  
O. Tarnowsky ◽  
A. F. Massardo

This paper investigates options for highly efficient SOFC hybrid systems of different sizes. For this purpose different models of pressurised SOFC hybrids systems have been developed in the framework of the European Project “LARGE SOFC - Towards a Large SOFC Power Plant”. This project, coordinated by VTT Finland, counts numerous industrial partners such as Wartsila, Topsoe and Rolls-Royce FCS ltd. Starting from the RRFCS Hybrid System [1], considered as the reference case, several plant modifications have been investigated in order to improve the thermodynamic efficiency. The main options considered are (i) the integration of a recuperated micro gas turbine and (ii) the replacement of the cathodic ejector with a blower. The plant layouts are analysed in order to define the optimum solution in terms of operating parameters and thermodynamic performances. The study of a large size power plant (around 110 MWe) fed by coal and incorporated with SOFC hybrid systems is also conducted. The aim of this study is to analyse the sustainability of an Integrated Gasification Hybrid System from the thermodynamic and economic point of view in the frame of future large sized power generation. A complete thermoeconomic analysis of the most promising plants is carried out, taking into account variable and capital costs of the systems. The designed systems are compared from the thermodynamic and the thermoeconomic point of view with some of the common technologies used for distributed generation (gas turbines and reciprocating engines) and large size power generation (combined cycles and IGCC). The tool used for this analysis is WTEMP software, developed by the University of Genoa (DIMSET-TPG) [2], able to carry out a detailed thermodynamic and thermoeconomic analysis of the whole plants.


2019 ◽  
Vol 2019 ◽  
pp. 1-16 ◽  
Author(s):  
Claudio Angione

In cell and molecular biology, metabolism is the only system that can be fully simulated at genome scale. Metabolic systems biology offers powerful abstraction tools to simulate all known metabolic reactions in a cell, therefore providing a snapshot that is close to its observable phenotype. In this review, we cover the 15 years of human metabolic modelling. We show that, although the past five years have not experienced large improvements in the size of the gene and metabolite sets in human metabolic models, their accuracy is rapidly increasing. We also describe how condition-, tissue-, and patient-specific metabolic models shed light on cell-specific changes occurring in the metabolic network, therefore predicting biomarkers of disease metabolism. We finally discuss current challenges and future promising directions for this research field, including machine/deep learning and precision medicine. In the omics era, profiling patients and biological processes from a multiomic point of view is becoming more common and less expensive. Starting from multiomic data collected from patients and N-of-1 trials where individual patients constitute different case studies, methods for model-building and data integration are being used to generate patient-specific models. Coupled with state-of-the-art machine learning methods, this will allow characterizing each patient’s disease phenotype and delivering precision medicine solutions, therefore leading to preventative medicine, reduced treatment, andin silicoclinical trials.


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