| Programming languages for synthetic biology. | |
| | |
MedLine Citation:
|
PMID: 22132053 Owner: NLM Status: In-Data-Review |
Abstract/OtherAbstract:
|
In the backdrop of accelerated efforts for creating synthetic organisms, the nature and scope of an ideal programming language for scripting synthetic organism in-silico has been receiving increasing attention. A few programming languages for synthetic biology capable of defining, constructing, networking, editing and delivering genome scale models of cellular processes have been recently attempted. All these represent important points in a spectrum of possibilities. This paper introduces Kera, a state of the art programming language for synthetic biology which is arguably ahead of similar languages or tools such as GEC, Antimony and GenoCAD. Kera is a full-fledged object oriented programming language which is tempered by biopart rule library named Samhita which captures the knowledge regarding the interaction of genome components and catalytic molecules. Prominent feature of the language are demonstrated through a toy example and the road map for the future development of Kera is also presented. |
| | |
Authors:
|
P Umesh; F Naveen; Chanchala Uma Maheswara Rao; Achuthsankar S Nair |
Related Documents
:
|
9597613 - Fluctuations in the number and distribution of prosthodontists: 1987-1995. 11785543 - Is training in psychology associated with increased responsiveness to suicidality? 4122093 - Pair: a cooperative effort to meet informational needs. |
Publication Detail:
|
Type: Journal Article Date: 2011-02-20 |
Journal Detail:
|
Title: Systems and synthetic biology Volume: 4 ISSN: 1872-5333 ISO Abbreviation: Syst Synth Biol Publication Date: 2010 Dec |
Date Detail:
|
Created Date: 2011-12-01 Completed Date: - Revised Date: - |
Medline Journal Info:
|
Nlm Unique ID: 101300404 Medline TA: Syst Synth Biol Country: Germany |
Other Details:
|
Languages: eng Pagination: 265-9 Citation Subset: - |
Export Citation:
|
APA/MLA Format Download EndNote Download BibTex |
| MeSH Terms | |
Descriptor/Qualifier:
|
|
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
Previous Document: Design of a novel nucleoside analog as potent inhibitor of the NAD dependent deacetylase, SIRT2.
Next Document: Sequence signatures of allosteric proteins towards rational design.