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More recently, a sRNA microarray approach allowed researchers to discover that 6S RNA is implicated in intracellular multiplication [19].
Secondly, the improved microarray approach allowed the additional detection of several differentially expressed genes, which are potentially important targets for further research.
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Therefore, this microarray approach allows genotypic resistance testing in a high-throughput manner with an accuracy that seems sufficient for routine clinical application.
Comparative analyses performed through a microarray-based approach allowed identification and characterization of large mobile genetic elements that seem to be exclusive to South American strains.
Moreover, the microarray approach provided allowed the discovery of a set of new potential chicken mature oocyte and chicken granulosa cell markers for future studies.
Note that this approach allowed us to compare tissue-specific expression across different microarray experiments.
Importantly, the higher sensitivity of this approach allowed us to resolve gametocyte-specific transcription in the large number of samples with gametocyte numbers below microarray detection limits.
This approach allowed the infection to spread.
That is, the SSH/microarray approach allowed about 100% more of the genes, most of which were low abundant, for the subsequent analyses.
Finally, this approach allowed us to test several replications of multiple doses and dilutions of the remedy, taking advantage of high-throughput and easily reproducible microarray technology.
This approach allowed for the detection of about ten times more of the differentially expressed genes than did the regular cDNA microarray approach in human hepatoma, particularly for those with low expression.
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