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The observing sequence is arranged randomly to realize non-uniform sampling in the cross-range dimensions of each target.
Instead of illuminating one target during the whole CPI, the pulses can be allocated to all the targets and the observing sequence is arranged randomly.
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The observed sequence changes within a species may reflect adaptations to different types of habitats or climates and distinguish geographically widely separated strains.
The observed sequence changes likely reflected unidirectional dHS-templated gene conversions, as an increase of green fluorescence was not observed in R5 cells, but would have been expected if a reciprocal exchange had introduced the first ATG codon into dHS.
The observed sequence similarity and phylogenetic tree topology allowed us to classify the MYB genes of soybean, Arabidopsis, and other plants into 47 subfamilies, which ranged in size from two to 28 MYB genes.
Instead, error probabilities are directly calculated by dividing the observed sequencing errors by total number of observations defined by the joint variables.
The coefficients of these functions can be estimated from the cross-correlation function or the auto-correlation functions of the two observed sequences by using the method presented in this paper.
To forecast the Ith event, we selected several modeled sequences that are able to accurately reproduce the observed event sequence up to the (I − 1 th event.
The observed filling sequence can be calculated by quantum mechanics.
Here, the null hypothesis is that the observed data sequence conforms to a random pattern, against the alternative that it does not.
The observed remarkable sequence divergence in the PDR5 gene in yeast strain YJM789 may represent an interesting case of adaptive loss of gene function with significant clinical implications.
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