Whole Gene Synthesis: A Gene-O-Matic Future

2005 ◽  
Vol 1 (1) ◽  
pp. 297-341 ◽  
Author(s):  
Lance Stewart ◽  
Alex B. Burgin
Keyword(s):  
1989 ◽  
Vol 264 (7) ◽  
pp. 4093-4103
Author(s):  
B P Monia ◽  
D J Ecker ◽  
S Jonnalagadda ◽  
J Marsh ◽  
L Gotlib ◽  
...  

Nature ◽  
2004 ◽  
Vol 432 (7020) ◽  
pp. 1050-1054 ◽  
Author(s):  
Jingdong Tian ◽  
Hui Gong ◽  
Nijing Sheng ◽  
Xiaochuan Zhou ◽  
Erdogan Gulari ◽  
...  
Keyword(s):  

2014 ◽  
Vol 34 (15) ◽  
pp. 10-10
Author(s):  
Gail Dutton
Keyword(s):  

2018 ◽  
Vol 3 (1) ◽  
Author(s):  
Subu K Subramanian ◽  
William P Russ ◽  
Rama Ranganathan

Abstract The design and synthesis of novel genes and deoxyribonucleic acid (DNA) sequences is a central technique in synthetic biology. Current methods of high throughput gene synthesis use pooled oligonucleotides obtained from custom-designed DNA microarray chips, and rely on orthogonal (non-interacting) polymerase chain reaction primers to specifically de-multiplex, by amplification, the precise subset of oligonucleotides necessary to assemble a full length gene. The availability of a large validated set of mutually orthogonal primers is therefore a crucial reagent for high-throughput gene synthesis. Here, we present a set of 166 20-nucleotide primers that are experimentally verified to be non-interacting, capable of specifying 13 695 unique genes. These primers represent a valuable resource to the synthetic biology community for specifying genetic components that can be assembled through a scalable and modular architecture.


2020 ◽  
Vol 9 (7) ◽  
pp. 1714-1724
Author(s):  
Claudia Chiocchini ◽  
Krishna Vattem ◽  
Michael Liss ◽  
Lisa Ludewig ◽  
Tobias Reusch ◽  
...  

2008 ◽  
Vol 26 (2) ◽  
pp. 121-134 ◽  
Author(s):  
Ai-Sheng Xiong ◽  
Ri-He Peng ◽  
Jing Zhuang ◽  
Jin-Ge Liu ◽  
Feng Gao ◽  
...  
Keyword(s):  

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