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As the G.A.O. and other institutions continue to examine these issues, additional problems and recommendations will likely be identified as well.
Additional variants will likely be identified.
Other mutations will likely be identified in the future.
From this correlation, renal response patterns will likely be identified with the purpose of developing a predictive model.
Other biological factors associated with their adaptation and tissue tropism in humans will likely be identified in the future.
However, the distribution patterns of cytosine methylation are not conserved in animals and independent molecular functions will likely be identified.
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Moreover, we will address discontinuous medical condition detection, which will most likely be identified through post-processing rules or an ensemble machine learning approach.
It is likely that we have captured the most severe cases of diabetes in the cohort; however, this may only strengthen the results, as any association will most likely be identified.
Therefore, assessing allelic variation in putative effectors between distinct PST isolates will likely be important to identify avirulence/virulence alleles.
Because power decreases as a function of allele frequency, very large sample sizes will likely be necessary to identify disease-association of rare variants.
While inferences to RRS in natural populations may be more difficult to make with these studies, experimental systems will likely be important for identifying the mechanisms responsible for differences in fitness between hatchery and wild fish.
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