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Further analyses based on set size, duplication type, synonymous substitution rate (Ks), and gene ontology emphasize shared and lineage-specific patterns of genome evolution via duplication.
Our analyses based on set size, duplication type, synonymous substitution rate (Ks), and gene ontology emphasize shared and lineage-specific patterns of genome evolution via gene duplication.
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This assertion is based on the set size effect observed in the data presented here, but also the set size effect reported by others (Gregg & Samuel, 2008; Eramudugolla et al., 2005; McAnally et al., 2010).
Two differentially expressed transcripts from two genes were selected based on probe set size consideration.
This sample size was based on setting statistical significance at 0.05 and 80% power.
Based on data set sizes of 1 million reads, the interquartile range which describes 50% of data, ranges from highly incomplete reconstructed mitogenomes (∼15% of the original size) to more complete mitogenomes (∼85% of the original size).
Cells were segmented based on nucleus size (set at 5 μm) and fluorescence intensity.
In this study, predictions based on sufficient probe set size and fold-change are confirmed by independent means.
We suggest that the function be designed as a dynamic adjustment based on the data set size and the order of interaction.
As apoptotic cells are sometimes condensed relative to normal cells, the threshold cannot be set based on the size of normal cells.
All specimens were live-sorted into gross morphospecies using a standard dissecting microscope (20x magnification) in a field laboratory setting based on colour, size, shape, collection date, and collection site.
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