Metabolic Network Dynamics: Properties and Principles

Author(s):  
Neema Jamshidi ◽  
Bernhard Ø. Palsson
2015 ◽  
Vol 10 (5) ◽  
pp. 100-118 ◽  
Author(s):  
D. Grigoriev ◽  
S. S. Samal ◽  
S. Vakulenko ◽  
A. Weber

2020 ◽  
Vol 21 (1) ◽  
Author(s):  
Lea F. Buchweitz ◽  
James T. Yurkovich ◽  
Christoph Blessing ◽  
Veronika Kohler ◽  
Fabian Schwarzkopf ◽  
...  

2002 ◽  
Vol 12 (2) ◽  
pp. 460-469 ◽  
Author(s):  
György Károlyi ◽  
István Scheuring ◽  
Tamás Czárán

2012 ◽  
Vol 10 (01) ◽  
pp. 1240003 ◽  
Author(s):  
ALI CAKMAK ◽  
XINJIAN QI ◽  
A. ERCUMENT CICEK ◽  
ILYA BEDERMAN ◽  
LEIGH HENDERSON ◽  
...  

With the recent advances in experimental technologies, such as gas chromatography and mass spectrometry, the number of metabolites that can be measured in biofluids of individuals has markedly increased. Given a set of such measurements, a very common task encountered by biologists is to identify the metabolic mechanisms that lead to changes in the concentrations of given metabolites and interpret the metabolic consequences of the observed changes in terms of physiological problems, nutritional deficiencies, or diseases. In this paper, we present the steady-state metabolic network dynamics analysis (SMDA) approach in detail, together with its application in a cystic fibrosis study. We also present a computational performance evaluation of the SMDA tool against a mammalian metabolic network database. The query output space of the SMDA tool is exponentially large in the number of reactions of the network. However, (i) larger numbers of observations exponentially reduce the output size, and (ii) exploratory search and browsing of the query output space is provided to allow users to search for what they are looking for.


2011 ◽  
Vol 156 (1) ◽  
pp. 346-356 ◽  
Author(s):  
Daoquan Xiang ◽  
Prakash Venglat ◽  
Chabane Tibiche ◽  
Hui Yang ◽  
Eddy Risseeuw ◽  
...  

2012 ◽  
Vol 10 (01) ◽  
pp. 1240004 ◽  
Author(s):  
A. ERCUMENT CICEK ◽  
GULTEKIN OZSOYOGLU

Steady state metabolic network dynamics analysis (SMDA) is a recently proposed computational metabolomics tool that (i) captures a metabolic network and its rules via a metabolic network database, (ii) mimics the reasoning of a biochemist, given a set of metabolic observations, and (iii) locates efficiently all possible metabolic activation/inactivation (flux) alternatives. However, a number of factors may cause the SMDA algorithm to eliminate feasible flux scenarios. These factors include (i) inherent error margins in observations (measurements), (ii) lack of knowledge to classify measurements as normal versus abnormal, and (iii) choosing a highly constrained metabolic subnetwork to query against. In this work, we first present and formalize these obstacles. Then, we propose techniques to eliminate them and present an experimental evaluation of our proposed techniques.


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