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The advent of Trachoma Rapid Assessment and Asymmetrical Sampling Rapid Trachoma Assessment has enabled faster identification of trachoma-endemic areas, though population-based surveys are still required prior to intervention.
Technology has enabled faster loan production through automation, ease of processing, and analytics.
The revolution in DNA sequencing technologies has enabled faster and cheaper data generation, to the point where data collection is becoming a less concerning bottleneck than data storage and analysis [1].
The additional training has enabled faster diagnosis and treatment of pneumonia.
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The development of a generic analytical SFC/MS screening protocol, following extensive evaluation of different stationary phase, modifier and gradient elution combinations, has enabled fast analytical method development for structurally diverse compounds within both specialised and high-throughput purification environments.
The introduction of image analysis with online grade measurements paired with the advanced process control by means of fuzzy logic has enabled fast, more precise control of the flotation process.
New developments in RSA have enabled faster analysis and even measurement of marker-free implants.
Therefore secreted CWDEs genes residing in plastic genome regions may have enabled faster adaptation to a new host or tissue (for instance, leaf vs root).
More recently, fast T1 assessment using a dual flip angle (FA) GRE sequence instead of a standard inversion recovery technique for dGEMRIC, 29 and GRE-based T2* mapping 24 as an alternative to the spin-echo-based T2 mapping approach, have enabled faster imaging times and isotropic three-dimensional (3D) cartilage evaluation.
Setting the cathode in the biotic tests at a low potential of −600 mV may have accelerated biofilm growth relative to open circuit controls, which could have enabled faster rates of corrosion via biodegradation of the carbon and metals compared to the controls.
CRISPR-Cas-based tools for genome editing and expression control have enabled fast, easy, and accurate strain development for established production platform organisms, such as Escherichia coli and Saccharomyces cerevisiae.
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CEO of Professional Science Editing for Scientists @ prosciediting.com