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The reason for the discrepancy in allele frequency between GSH1 and the other five mutations from UV mutant population sequencing is unknown but may be a population sequencing artefact.
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The function, if any, of most of the rest of the sequence is unknown.
Amplification of repetitive sequences is therefore frequently used in absolute quantification but problems occur in relative quantification as the number of repetitive sequences is unknown.
In incremental learning, the consistency between the existing internal representation and a new sequence is unknown, so it is not appropriate to overwrite the existing internal representation on each new sequence.
While the precise functional significance of this transcription factor expression sequence is unknown, its common appearance in embryonic and adult neurogenesis, and in different brain regions, suggests it is part of a conserved genetic program that specifies general properties of glutamatergic neurons in these regions.
As traffic channels are not emitted at constant power and may employ frequency hopping, one might initially conclude that they will not useful for localization (as the hopping sequence is unknown, an RSS value in this case just represents the observed power at a given frequency, averaged over a few GSM frames).
The order of the sequence is unknown.
However, the order of the sequence is unknown.
Whether selection is acting, or has acted, on the nov sequences is unknown.
The driving force underlying the insertion of these potentially harmful sequences is unknown.
The biological significance for the presence of two distinctive, dominant forms of VP1 unique sequence is unknown.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com