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As VIA methods offer data representation on a continuous rather than a quantal scale, the data interpretation is potentially more biologically realistic.
This is a pivotal departure from other storage formats because objects simultaneously provide an informational component (via properties), as do other formats, but also a manipulation component (via methods) that is unattainable for textual and markup-based representations.
Overall, selection bias and error are perhaps inherent to a greater degree in the standard quantal visual scale method estimates, than computerized VIA methods, for the reasons given above.
Although selection of the path for video scanning is a potential source of error with the above VIA methods, the selection of a grade for immunostained cellular density utilizes broader assumptions and is in fact more liable to selection error.
It was noted that VIA methods could discriminate between infiltrates designated as identical using direct visual methods, both in terms of offering a continuous scale and providing qualitative information regarding the cell distribution.
The quantitation of cell density using the VIA methods described here relies on the valid approximation that measurement of the total reaction product viewed in a video field (in pixels) is virtually identical to measurement of the summated reaction product (in pixels) around the isolated, individual cells within that same field.
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Each rule can be seen as a list of constraints; a constraint is responsible for checking if its precondition is valid (via method check), and for applying its postcondition on a membrane (via method apply).
Ksop was calculated via method reported by Asgari et al. (2013).
We find that the models obtained via method B have smaller pores as compared to the models obtained via method A. This is reflected in the adsorption properties.
In this section, we present estimates of the parameters of the EKD distribution via method of maximum likelihood estimation.
These were then converted into the indanamines 8xvi– xxi via method B (Scheme 1).
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