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However, information on repeated acceleration sequences is currently limited.
The development of methods for inferring and dating phylogenies from gene sequences is currently an active area of research.
The initial paper by Macdonald et al. even acknowledges that their criteria should not be applied to non-enhancing tumor.[4] As such, our method still represents an advance over current assessment techniques, and modification of our program to incorporate T2/FLAIR MRI sequences is currently being attempted to address this limitation.
Observations of interest occur in the final pair of odors (e.g. observation "at pair 5, not responding to an odor, not sampling an odor" or (5,0,0)), where the agent must recall which of the two odor sequences is currently being presented.
Only a miniscule fraction of the existing phage and plasmid sequences is currently available, whereas the total diversity of prokaryotic mobile elements is humungous and apparently exceeds the diversity of prokaryotes at least by an order of magnitude [ 41, 42].
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Complementary sets of sequences are currently being applied to signal coding, radar, and multi-user systems, among others.
In Egypt, HEV seroprevalence is among the highest in the world; however, only a very limited number of Egyptian HEV sequences are currently available.
Nevertheless, conventional MRI sequences, as T1-weightened sequences, are currently considered not precise enough to detect brain structural anomalies in this context, and therefore are supposed to be unable to accurately predict outcome1.
Few LSU rRNA sequences are currently available for protists.
S. suis is phylogenetically distinct from other Streptococcus species for which genome sequences are currently available.
Nevertheless, twenty of these twenty-two genome sequences are currently available only as low- coverage (∼2×) assemblies (Table 1), produced using traditional, capillary sequencing methods.
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