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Jean-Christophe Baret

Researcher at Institut Universitaire de France

Publications -  101
Citations -  12354

Jean-Christophe Baret is an academic researcher from Institut Universitaire de France. The author has contributed to research in topics: Microfluidics & Electrowetting. The author has an hindex of 41, co-authored 97 publications receiving 10766 citations. Previous affiliations of Jean-Christophe Baret include Max Planck Society & University of Twente.

Papers
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Electrowetting: from basics to applications

TL;DR: In this paper, the authors compare the various approaches used to derive the basic electrowetting equation, which has been shown to be very reliable as long as the applied voltage is not too high.
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Ultrahigh-throughput screening in drop-based microfluidics for directed evolution

TL;DR: This work presents a general ultrahigh-throughput screening platform using drop-based microfluidics that overcomes limitations and revolutionizes both the scale and speed of screening.
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Fluorescence-activated droplet sorting (FADS): efficient microfluidic cell sorting based on enzymatic activity

TL;DR: A theoretical model based on the Poisson distribution accurately predicted the observed enrichment values using the starting cell density (cells per droplet) and the ratio of active to inactive cells, and all of the recovered cells were the active strain.
Journal Article

Correction for Ultrahigh-throughput screening in drop-based microfluidics for directed evolution

TL;DR: In this article, a drop-based microfluidics-based screening platform using aqueous drops dispersed in oil as picoliter-volume reaction vessels was proposed to identify new mutants of the enzyme horseradish peroxidase.
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Droplet-Based Microfluidic Platforms for the Encapsulation and Screening of Mammalian Cells and Multicellular Organisms

TL;DR: Droplet-based microfluidic platforms in which cells are grown in aqueous microcompartments separated by an inert perfluorocarbon carrier oil are described, which should open the way for high-throughput, cell-based screening that can use >1000-fold smaller assay volumes and has approximately 500x higher throughput than conventional microtiter plate assays.