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Even more sequences will flow from ongoing and future metagenomic projects.
Because of the conservative nature of "test 2" (see Methods and [29]), and because the average synonymous rate was 4.105 (excluding root branches) in the ε/γ data set, more sequences will be required to definitely rule out the action of positive selection during the evolution of the ε subunit.
These sequences will be tagged as STEVOR-like until the availability of more sequences will allow for better categorization.
Probably more sequences will be identified once full genome sequencing data will be available in open access databases.
Cases when one primer pair results in two or more sequences will be interpreted as a draw that accidentally results in more than one ball.
However, due to the patchiness of the database for eukaryotic sequences, this result could change in the future when more sequences will be available for eukaryotic species.
Similar(52)
More sequencing will primarily uncover more sites of the lower-affinity class.
However, it also means that more sequencing will be required to capture the rare insertions (see [164]).
The availability of more and more genome sequences will also open the way to a comparative analysis of metabolism.
To summarize our analysis so far, relatively few functions are carried out by multiple structures, but this number would increase as more protein sequences will become characterized.
Until now, the molecular mechanism of RovA-dependent transcription of the target genes has only been determined for two genes, inv and rovA, and the analysis of more target sequences will obviously be required to fully characterize a RovA binding site.
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