dc.contributor.advisor | Ron Weiss. | en_US |
dc.contributor.author | Elias, Blake Marshal | en_US |
dc.contributor.other | Massachusetts Institute of Technology. Department of Electrical Engineering and Computer Science. | en_US |
dc.date.accessioned | 2018-12-18T19:48:57Z | |
dc.date.available | 2018-12-18T19:48:57Z | |
dc.date.copyright | 2018 | en_US |
dc.date.issued | 2018 | en_US |
dc.identifier.uri | http://hdl.handle.net/1721.1/119762 | |
dc.description | Thesis: M. Eng., Massachusetts Institute of Technology, Department of Electrical Engineering and Computer Science, 2018. | en_US |
dc.description | This electronic version was submitted by the student author. The certified thesis is available in the Institute Archives and Special Collections. | en_US |
dc.description | Cataloged from student-submitted PDF version of thesis. | en_US |
dc.description | Includes bibliographical references (pages 129-132). | en_US |
dc.description.abstract | Synthetic biology is the artificial design and engineering of biological systems and living organisms, drawing from disciplines such as biological and electrical engineering, computer science, biology and chemistry. Experimental work in synthetic biology is enabled by molecular biology techniques such as DNA assembly and molecular cloning. Researchers currently perform these techniques manually in wet-labs, which is expensive, time-consuming, requires extensive training and is unreliable. This thesis demonstrates a working robotic automation system that lowers the monetary- and time-cost of performing synthetic biology experiments, reduces the volume of Golden Gate DNA Assembly reactions by an order of magnitude using pin tools for small-volume liquid transfer, and which has successfully built 130 new genetic constructs using 192 genetic parts submitted by 11 researchers for both bacterial and mammalian systems. This thesis also presents a model which uses data on past assembly success to predict the outcome of reactions that the model had not seen. This model generates two sub-libraries of validated parts: one containing 79 parts (41% of those submitted) with a predicted assembly success rate of 90% or greater, the other with 28 parts (15% of those submitted) and 99% or greater predicted success, when using parts exclusively within each of the respective libraries. | en_US |
dc.description.statementofresponsibility | by Blake Marshal Elias. | en_US |
dc.format.extent | 132 pages | en_US |
dc.language.iso | eng | en_US |
dc.publisher | Massachusetts Institute of Technology | en_US |
dc.rights | MIT theses are protected by copyright. They may be viewed, downloaded, or printed from this source but further reproduction or distribution in any format is prohibited without written permission. | en_US |
dc.rights.uri | http://dspace.mit.edu/handle/1721.1/7582 | en_US |
dc.subject | Electrical Engineering and Computer Science. | en_US |
dc.title | High throughput pin-tool based automated DNA assembly | en_US |
dc.type | Thesis | en_US |
dc.description.degree | M. Eng. | en_US |
dc.contributor.department | Massachusetts Institute of Technology. Department of Electrical Engineering and Computer Science | |
dc.identifier.oclc | 1078783280 | en_US |