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Relevant colocations (i.e. genes in the QTL confidence interval and functionally related to the trait) were observed on chromosomes 1, 2, 3, 4, 5, 6, 7 and 9 (Table 3).
Similar(59)
Similar pattern for each trait was observed in the other five environments (Additional file 1: Table S8).
A slight distortion in genetic segregation for the trait was observed and this may be due to the preferential fertilization of a particular gametic genotype.
This trait was observed in an experimentally induced resistant strain of S. cerevisiae that was selected for fluconazole tolerance after growth for 400 generations in the presence of the drug [9] and was also observed in three different clinical isolates of Candida albicans that developed fluconazole resistance [10].
Overall, the transfer of at least 1 resistant trait was observed in 37 cases (47%).
Generations overlapped, selection was for a single trait, and the trait was observed for all selection candidates prior to selection.
This approach could be transferred to a situation in which only one trait is observed, provided that EBV of the individuals have heterogeneous accuracies.
While the level of spotting was not analyzed in the linkage mapping population, variation in this trait was observed in the F2/Backcross generation.
To investigate whether this trait is observed more broadly in the Myriapoda, we have assayed cases noted from that species in the T. corallinus genome.
This trait was observed in other AAB including most of those described as insect symbionts (i.e., Ac. tropicalis, C. intestini, Glucona. diazotrophicus, Glucona. europaeus, Glucona. oboediens, G. frateurii, G. morbifer, G. Oxydans, and G. thailandicus).
Significant correlations between these four traits were observed in the germplasm collection (Additional file 2).
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CEO of Professional Science Editing for Scientists @ prosciediting.com