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Both methods we described are efficient and each of them has its own advantages.
The human melanocyte cell line UM-U-95 was obtained from the choroid of healthy Caucasian donor eyes using the methods we described previously [29].
GST tags were used according to the methods we described previously [ 17].
To improve upon these methods, we described logarithmic intensity-based motion contrast methods and demonstrated their superiority for in vivo human parafoveal microvasculature visualization.
The methods we described do not consider mechanistic aspects, but simply use transcriptional signatures as readouts from the 'black-box' of cellular mechanisms.
Using detailed analyses of waveform components, voltage topographies and source localisation methods, we described the spatiotemporal propagation of SSEPs across the brain and demonstrated the stability of EEG recordings over time and across animals.
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In 'Data and methods' , we describe the two datasets used.
The distinction is unnecessary for the methods we describe.
Meanwhile, in the framework of the standard additive Schwarz methods, we describe this method by a complete variational form.
For all the methods we describe, the communication between the MSs and RSs is made through the cooperative link.
In Section "Methods" we describe the design of the study, outline our data set and perform some exploratory data analysis.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com