CREATE specifications


Unique identifier OMICS_14819
Alternative name CRISPR-enabled trackable genome engineering
Interface Web user interface
Restrictions to use None
Input data The organism, the gene name, the library name, the nucleotide sequence, the length of buffer sequence before start codon, the targeted amino acid residues.
Output data The edited cassettes.
Computer skills Basic
Stability Stable
Maintained Yes


  • Bacteria
    • Escherichia coli


  • person_outline Ryan Gill

Publication for CRISPR-enabled trackable genome engineering

CREATE institution(s)
Department of Chemical and Biological Engineering, University of Colorado Boulder, Boulder, CO, USA; Muse Biotechnology Inc., Boulder, CO, USA; Department of Molecular, Cellular and Developmental Biology, University of Colorado Boulder, Boulder, CO, USA; Department of Biochemical Engineering, School of Chemical Engineering and Technology, Tianjin University, Tianjin, China; SynBio Research Platform, Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin University, Tianjin, China; Key Laboratory of Systems Bioengineering (Ministry of Education), Tianjin University, Tianjin, China
CREATE funding source(s)
This work was supported by the US Department of Energy (Grant DE-SC0008812) and CAPES foundation (grant #0315133).

CREATE reviews

star_border star_border star_border star_border star_border
star star star star star

Be the first to review CREATE