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Nowadays, the extensive use of different high-throughput methodologies allows the obtention of different measurements for the genes such as methylation status, splicing variants, linkage to diseases, etc., in a straightforward manner.
Therefore, applying these methodologies allows the selection of causal structures without relying on prior knowledge alone.
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All methodologies allowed the recommendations of the official methods.
Furthermore, the proposed methodologies allowed the determination of the CdSe QDs diameters.
The herein proposed methodologies allow the reliable determination of very low nanoparticle concentrations.
Imaging mass spectrometry coupled to peptidomic and lipidomic methodologies allowed the selection of molecules whose spatiotemporal pattern of expression was of potential interest.
Extensive purification of blad and sequencing of its N- and C- terminals, as well as of several internal sequences by conventional methodologies allowed the precise location of the nucleotide sequence encoding blad within that of its precursor (Figure 1).
Combining the results of both methodologies allowed the estimation of the incidence of post-F1 hybridisation and back-crossing.
In this context, there is an obvious need for methodologies allowing the low-cost, fast and high-throughput genotyping of virtually any species, such as the Diversity Arrays Technology (DArT).
In this context, there is an obvious need for new methodologies allowing the low-cost, fast and high-throughput genotyping of virtually any species.
The methodology allows the calculation of the emissions affecting the considered impact categories.
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CEO of Professional Science Editing for Scientists @ prosciediting.com