MAGE and CRISPR/Cas systems are increasingly used for large-scale genome engineering.
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Population based omics tools are optimized for higher throughputs but lack single cell resolution.
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Nanoliter-scale capsule or droplet reactors can be used for high-throughput single cell screening.
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Microchips allow ultra-high throughput picoliter-scale single cell phenotyping.
Genetic engineering and screening of large number of cells or populations is a crucial bottleneck in today’s systems biology and applied (micro)biology. Instead of using standard methods in bottles, flasks or 96-well plates, scientists are increasingly relying on high-throughput strategies that miniaturize their experiments to the nanoliter and picoliter scale and the single-cell level. In this review, we summarize different high-throughput system-wide genome engineering and screening strategies for microbes. More specifically, we will emphasize the use of multiplex automated genome evolution (MAGE) and CRISPR/Cas systems for high-throughput genome engineering and the application of (lab-on-chip) nanoreactors for high-throughput single-cell or population screening.