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These two methods will thus be worthwhile tools in the specific detection of F. langsethiae in infected crops.
CRISPR-, VNTR-, and other related genotyping methods will thus likely remain important genotyping tools for epidemiological purposes.
New computational methods will thus be required to address this shortcoming.
Efficient genotyping methods will thus yield further insights into somatic retrotransposition.
Innovative methods will thus continue to be needed to exploit available data.
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For example, for the seventh iteration, 22 centers are produced by VQA, each interpolation method will thus generate N=(10000−22)×365 predictions.
An iterative numerical method will thus be introduced to solve this deficiency, resulting in the third version of (varDelta _{mathrm{eq}}).
A direct effect of the anonymization process is an increase in the concentration of trajectories (i.e. several original trajectories are bundled on the same route); the clustering method will thus be influenced by the variation in the density distribution.
This method will, thus, enable us to integrate different types of histological data in the same coordinate for quantitative analyses.
HYDEqPCR can detect low-level Map shedders that go undetected using these other methods, which will thus underestimate the proportions of Map-shedders in herds.
However, they can easily be replaced with more advanced state-of-the-art methods and will thus produce more robust results in difficult environments.
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