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From the user-journey mapping, we identify some key behaviour change techniques that could be applied, primarily by cookstove implementers, at different phases in the adoption journey to support users in the process of overcoming behavioural barriers to adopting a new technology.
Furthermore, through epitope mapping, we identify two distinct epitopes on H5 HA molecule recognized by these rhAbs and demonstrate their potential to protect against a lethal H5N1 virus infection in a mouse model.
Using genetic linkage mapping, we identify regions of the genome that influence different aspects of lateral line morphology.
With respect to the lineage-tissue mapping we identify a minimal set of requirements so as to ensure that the widest possible class of cross-level principles is covered.
Using a genome-wide association study in C. elegans wild populations and quantitative trait locus mapping, we identify a 159 base-pair deletion in the conserved drh-1 gene (encoding a RIG-I-like helicase) as a major determinant of viral sensitivity.
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Using zip code data and using geographic mapping, we identified two main clusters where injuries were occurring.
In this systematic mapping, we identified 18 survey papers associated to the theme text mining and semantics [14 31].
By employing an energy-based approach to identify ligand binding sites, and comparison with the results of computational solvent mapping, we identified two potential ligandable sites in the active toxin which can be targeted during structure-based drug design against cholera.
Using candidate gene association mapping, we identified that this non-synonymous polymorphism was associated with IDH activity variation.
Using association mapping, we identified that this variation in one case is related to heritable enzyme activity variation.
Through interval mapping, we identified a single significant QTL on mouse chromosome 7 for corpus callosum volume with a QTL peak located between 25.5 and 26.7 Mb.
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