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Once the samples are mounted, sanded and ready to be analyzed, the rings of every sample need to be dated.
After the etching of Si3N4, the PMMA and Cr remained on the sample need to be removed.
Real-time PCR, however, encounters technical difficulties when multiple mutations from one sample need to be detected simultaneously in a single tube.
A more specific study about the optical properties of the sample need to be further investigated.
In order to reconstruct the pedigree of a sample, the parents of each individual in the sample need to be determined.
In order to merge such single-sample calls into one dataset, variants not called in one sample need to be assumed as either homozygous reference, or set to missing.
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It is one area where future research, based on a larger sample, needs to be explored.
This study sample needs to be larger and more representative of the two populations.
Whenever a new sample needs to be added to the delay line all the values need to be shifted down.
When crudely observing cyclicality from the summary statistics, the aging of the sample needs to be kept in mind.
Before mixing with the nitrocellulose-based ink, the stored Cu NWs sample needed to be purified from PVP and DEHA.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com