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The 16S 23S gene internal transcribed spacer sequence of sixty-four strains belonging to different acetic acid bacteria genera were analyzed, and phylogenetic trees were generated for each genera.
To calculate the number of anode electrons harvested, the recorded voltage curves for each genera were converted to amps of current using Ohm's Law (I = V/R).
The electrogenic yield for each genera was calculated as the ratio of electrons passing through the electrical circuit of the MFC to the total electrons associated with the known photon flux illuminating the 50 cm2 anode surface.
We tried to choose at least two species for each genera, except for monotypic genera; however, only one species was available for several genera, including Auriglobus, Marilyna, Omegophora, Pelagocephalus, and Tetractenos.
N EST, number of EST sequences downloaded for each genera; di-, tetra-,etra-, pentandand hexa- denotes type of SSRs and total indicates the total number of SSRs with primer information found for each genera.
The results obtained by the software were also used for the prediction of the pan-, dispensable- and core-genome [ 57] of each genera and the family [ 58].
Similar(49)
Artemisia, Malva, Poa and Veronica were represented by three species each, 20 genera by two species each and 85 (77.27%) genera were represented by just one species each.
Pure and mixed (E. coli + S. typhi), (E. coli + Sh. flexneri) bacterial cultures were used with each ciliate genera to evaluate the following: predator duplication rate, prey reduction rate, clearance rate and net grazing rate.
We also evaluated the relative abundance of each ant genera (overall, by sampling method, and within our three strata of interest) based on their number of occurrences in samples.
For each assemblage genera were counted only once and higher taxa (i.e., generically indeterminate remains) were counted only if the group was not represented by generic remains, unless published reports provided a reasonable case that the remains represent distinct taxa.
Phylogenetic analysis indicated that the Vtg gene family arose by unique duplication events in each mosquito genera.
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