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Open collaborative system design : a strategic framework with application to synthetic biology

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dc.contributor.advisor Edward F. Crawley. en_US
dc.contributor.author Silver, Matthew Robin en_US
dc.contributor.other Massachusetts Institute of Technology. Engineering Systems Division. en_US
dc.date.accessioned 2011-05-23T18:01:57Z
dc.date.available 2011-05-23T18:01:57Z
dc.date.copyright 2010 en_US
dc.date.issued 2010 en_US
dc.identifier.uri http://hdl.handle.net/1721.1/63012
dc.description Thesis (Ph. D.)--Massachusetts Institute of Technology, Engineering Systems Division, 2010. en_US
dc.description Cataloged from PDF version of thesis. en_US
dc.description Includes bibliographical references (p. 251-259). en_US
dc.description.abstract Across technology industries and particularly at the cutting edge of biotechnology a debate is under way about the proper balance between open and closed - between co-developing products with shared information and open standards, versus using more traditional, closed, proprietary processes. Beyond the relative success of open source software to date, it is not clear how and whether open design processes might be applied generally for complex, assembled technologies. This problem takes on special urgency within the domain of synthetic biology, an emerging discipline in which many practitioners advocate opening design and development through platforms such as the registry of standardized biological parts. Biotechnology is IP intensive in part because commercialization is complicated and capital intensive. How might one develop a sustainable open development process in this context? This thesis addresses these questions from an Engineering Systems perspective. Defining open, collaborative system development (OCSD) specifically as a process in which subsystems are created voluntarily by an unrestricted set of third-party contributors, it makes the following claim: An OCSD process can itself be designed, with the principal objective of creating an environment for third-party innovation. To support this claim the thesis outlines a conceptual framework to guide OCSD design. The framework includes a taxonomy of parameters and constraints relevant to opening design, a list of options within each taxonomic category, and three high level strategies found to recur as a function of sponsor goals and technological constraints. Finally, the thesis proposes a quantitative method, based on multidisciplinary modeling and pareto analysis, to design open standards within the context of one of the three strategies. The research is carried out through a pragmatic blend of case studies and quantitative modeling. First, an in-depth, multi-discipline literature review synthesizes relevant taxonomic categories. Thirteen examples of OCSD spanning nine industries are then analyzed to define options within each taxonomic category. The case studies are also used to identify strategies for opening design based on correlations between OCSD options. The framework is validated and expanded through an in-depth case study of the opening of Very Large Scale Integration (VLSI) in the semi-conductor industry in the late 1970s. Finally, a quantitative method is developed to guide the design of open standards within one of the three strategies. These three contributions - the framework, correlated strategies, and quantitative method - are then applied to a particular biotechnology called microbial fuel cells. en_US
dc.description.statementofresponsibility by Matthew Robin Silver. en_US
dc.format.extent 259 p. en_US
dc.language.iso eng en_US
dc.publisher Massachusetts Institute of Technology en_US
dc.rights M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission. en_US
dc.rights.uri http://dspace.mit.edu/handle/1721.1/7582 en_US
dc.subject Engineering Systems Division. en_US
dc.title Open collaborative system design : a strategic framework with application to synthetic biology en_US
dc.type Thesis en_US
dc.description.degree Ph.D. en_US
dc.contributor.department Massachusetts Institute of Technology. Engineering Systems Division. en_US
dc.identifier.oclc 720919566 en_US


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