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Large scale active-learning-guided exploration for in vitro protein production optimization.

Olivier Borkowski | Mathilde Koch | Agnès Zettor | Amir Pandi | Angelo Cardoso Batista | Paul Soudier | Jean-Loup Faulon
Nature communications | 2020

Lysate-based cell-free systems have become a major platform to study gene expression but batch-to-batch variation makes protein production difficult to predict. Here we describe an active learning approach to explore a combinatorial space of ~4,000,000 cell-free buffer compositions, maximizing protein production and identifying critical parameters involved in cell-free productivity. We also provide a one-step-method to achieve high quality predictions for protein production using minimal experimental effort regardless of the lysate quality.

Pubmed ID: 32312991

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Associated grants

  • Agency: Biotechnology and Biological Sciences Research Council, United Kingdom
    Id: BB/M017702/1

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ECHO (tool)

RRID:SCR_011851

Error correction algorithm designed for short-reads from next-generation sequencing platforms such as Illumina''s Genome Analyzer II.

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