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Logistic-Generalized Linear Models (GLMs) were used to develop species distribution models (SDM) of seagrass meadows and single species.
We used an extensive set of caribou locations (5 subpopulations, 102 animals, 270,808 GPS-collar locations) collected over 11 years within the Central Mountain Designatable Unit to develop species distribution models that quantified avoidance by caribou of anthropogenic and natural disturbance features.
However, there was a set of taxa (those marked with + in Table 3) for which we were not able to develop species distributions models due to either lack of samples or to the distribution of those samples.
Therefore, it is crucial to develop species specific diagnostic test for all of these species and we believe that, this can be possible with short peptides identified by phage display technique as reported here.
This approach enabled us to develop species specific phylogenetic framework.
The identified SFPs may serve as targets of future efforts to develop species- specific genetic control strategies.
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The objective of this study was to develop species-specific PCR based on the gyrB gene sequence for direct species identification of the C. sakazakii and Cronobacter dublinensis within the C. sakazakii group.
The aim of this study was to use tuf gene as a molecular target for species discrimination in the Acetobacter genus, as well as to develop species-specific PCR method for direct species identification of Acetobacter aceti.
The objective of this study was to develop species-specific primers based on randomly amplified polymorphic DNA (RAPD) fingerprinting to distinguish species within the closely related Lactobacillus plantarum group.
The objective of this study was to develop species-specific PCR based on the gyrB gene sequence for direct species identification of the B. licheniformis within the B. subtilis group.
This work aimed to determine the inter- and intra-specific variations in populations of Bulinus truncatus and Bulinus beccari, the intermediate hosts of Schistosoma haematobium in Saudi Arabia, and to develop species-specific primers to identify these snails as a first step in the development of multiplex PCR for simultaneously identifying the snails and diagnosing its infections in a single step.
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