{"database":"biostudies-other","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["10"],"submitter":["Lucian Smith"],"journal":["BMC systems biology"],"pagination":["27"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/MODEL1511290000"],"repository":["biostudies-other"],"additional_accession":["26968941"],"pubmed_authors":["administrator","Lucian Smith","Alejandro Vignoni"]},"is_claimable":false,"name":"Boada2016 - Incoherent type 1 feed-forward loop (I1-FFL)","description":"<notes xmlns=\"http://www.sbml.org/sbml/level2/version4\">      <body xmlns=\"http://www.w3.org/1999/xhtml\">        <div class=\"dc:title\">Boada2016 - Incoherent type 1 feed-forwardloop (I1-FFL)</div><div class=\"dc:description\">A synthetic-biology mathematicalmodelling framework that was constructed to provide guidelines forexperimental implementation and parameter optimisation resulted ina biological device demonstrating desired behaviour.<br /></div><div class=\"dc:bibliographicCitation\">  <p>This model is described in the article:</p>  <div class=\"bibo:title\">    <a href=\"http://identifiers.org/pubmed/26968941\" title=\"Access to this publication\">Multi-objective optimization    framework to obtain model-based guidelines for tuning    biological synthetic devices: an adaptive network case.</a>  </div>  <div class=\"bibo:authorList\">Boada Y, Reynoso-Meza G, Picó  J, Vignoni A.</div>  <div class=\"bibo:Journal\">BMC Syst Biol 2016 Mar; 10: 27</div>  <p>Abstract:</p>  <div class=\"bibo:abstract\">    <p>Model based design plays a fundamental role in synthetic    biology. Exploiting modularity, i.e. using biological parts and    interconnecting them to build new and more complex biological    circuits is one of the key issues. In this context,    mathematical models have been used to generate predictions of    the behavior of the designed device. Designers not only want    the ability to predict the circuit behavior once all its    components have been determined, but also to help on the design    and selection of its biological parts, i.e. to provide    guidelines for the experimental implementation. This is    tantamount to obtaining proper values of the model parameters,    for the circuit behavior results from the interplay between    model structure and parameters tuning. However, determining    crisp values for parameters of the involved parts is not a    realistic approach. Uncertainty is ubiquitous to biology, and    the characterization of biological parts is not exempt from it.    Moreover, the desired dynamical behavior for the designed    circuit usually results from a trade-off among several goals to    be optimized.We propose the use of a multi-objective    optimization tuning framework to get a model-based set of    guidelines for the selection of the kinetic parameters required    to build a biological device with desired behavior. The design    criteria are encoded in the formulation of the objectives and    optimization problem itself. As a result, on the one hand the    designer obtains qualitative regions/intervals of values of the    circuit parameters giving rise to the predefined circuit    behavior; on the other hand, he obtains useful information for    its guidance in the implementation process. These parameters    are chosen so that they can effectively be tuned at the    wet-lab, i.e. they are effective biological tuning knobs. To    show the proposed approach, the methodology is applied to the    design of a well known biological circuit: a genetic incoherent    feed-forward circuit showing adaptive behavior.The proposed    multi-objective optimization design framework is able to    provide effective guidelines to tune biological parameters so    as to achieve a desired circuit behavior. Moreover, it is easy    to analyze the impact of the context on the synthetic device to    be designed. That is, one can analyze how the presence of a    downstream load influences the performance of the designed    circuit, and take it into account.</p>  </div></div><div class=\"dc:publisher\">  <p>This model is hosted on   <a href=\"http://www.ebi.ac.uk/biomodels/\">BioModels Database</a>  and identified by:   <a href=\"http://identifiers.org/biomodels.db/BIOMD0000000696\">BIOMD0000000696</a>.</p>  <p>To cite BioModels Database, please use:   <a href=\"http://identifiers.org/pubmed/25414348\" target=\"_blank\">Chelliah V et al. BioModels: ten-year  anniversary. Nucl. Acids Res. 2015, 43(Database  issue):D542-8</a>.</p></div><div class=\"dc:license\">  <p>To the extent possible under law, all copyright and related or  neighbouring rights to this encoded model have been dedicated to  the public domain worldwide. Please refer to   <a href=\"http://creativecommons.org/publicdomain/zero/1.0/\" title=\"Access to: CC0 1.0 Universal (CC0 1.0), Public Domain Dedication\">CC0  Public Domain Dedication</a> for more information.</p></div></body>    </notes>","dates":{"release":"2015-11-29T00:00:00Z","modification":"2025-07-15T09:55:17.23Z","creation":"2025-03-29T18:28:00.753Z"},"accession":"MODEL1511290000","cross_references":{"biomodels___db":["BIOMD0000000696"],"sbo":["SBO:0000341","SBO:0000485","SBO:0000183","SBO:0000607","SBO:0000338","SBO:0000468","SBO:0000004","SBO:0000179"],"pubmed":["26968941"],"pr":["PR:000000001"],"ncit":["C19061","C94928","C48918","C97201","C82333","C49142","C63845","C120268"],"mamo":["MAMO_0000046"],"obi":["OBI:0100060","OBI:0001180"],"go":["GO:0005576","GO:0006810","GO:0006412"],"cl":["CL:0000000"],"so":["SO:0000234"],"efo":["EFO:EFO:0001773"]}}