作者: Emily C. Mundorff , Jeremy S. Minshull , Sridhar Govindarajan , Claes Gustafsson
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摘要: Methods and devices for more efficiently engineering diversity into recombinant polypeptides and/or nucleic acids are provided herein. For example, a variety of methods selecting assessing potential crossover sites in an amino acid sequence or nucleotide provided, as well the resulting chimeric product sequences. These include, e.g., consideration structural, functional statistical data selection assessment sequences use recombination.