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Furthermore, the analysis has also allowed us to identify two sets of standards viz.
Our analysis has also allowed us to reconstruct the changes in the ecology of the genus.
Including interactions in the analysis has also allowed mapping of several other loci, including Cia41 and Cia42 in mouse and Cia26 in rats [ 60, 68].
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Morphological analysis have also allowed better determining the cellular localization of this protein in the deep side of the tumor, and this can explain why in biological samples, such as scraping and saliva, it was not possible to determine the overexpression of this marker.
Quantitative pyrosequencing-based analysis of mutation burden has also allowed us to more accurately investigate correlations between mutation burden and key clinico-pathological parameters.
The analysis developed with the FEM modeling has also allowed highlighting that the hypothesis adopted by using the simplified model (i.e., the hypothesis of linear relationship between the stress application frequency and the dynamic damping) is valid for frequencies higher than 75 Hz or at high speeds (>250 km/h).
This arrangement has also allowed comparative analysis of our data with those from the TIGR4 STM study [10].
This knowledge has guided our analysis of Bcl-G-deficient mice and has also allowed us to investigate biochemical properties of this protein.
The flexible modelling framework has also allowed us to conduct a detailed sensitivity analysis to test the effect of critical assumptions in the model reconstructions.
The initiative has also allowed researchers to hurdle many of the barricades that have hindered accurate analysis such as the lack of reference standards and comparative data.
Optical mapping has also allowed for detailed placement of BAC clones initially localised to chromosomes through admixture mapping analysis [ 22, 23].
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