We use next generation sequencing throughout library construction and downstream selection output analyses. This allows us to directly measure the diversity of each exclusive library we build, to ensure it reaches our high standards.

By applying NGS and AbXtract, our in-house bioinformatic analysis platform, to selection outputs, we are usually able to identify one hundred to one thousand different clusters. Once representative cluster sequences have been identified, gene synthesis is used to go “from sequence to clone”, allowing access to the most promising leads.