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The down-regulation of NTCP expression observed in microarrays was confirmed at the activity level.
The absence of genes as established with microarrays, was confirmed by PCR.
As shown in Figure 2B, the clec-67 upregulation by S. enterica observed in our microarrays was confirmed by qRT-PCR.
The miRNA expression observed by microarrays was confirmed by qRT-PCR (see Supplementary Figure S4).
Overall gene expression data obtained using cDNA microarrays was confirmed in qRT-PCR experiments for over 80% of the genes tested, even when the target RNA derived from a distinct biological replicate.
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The results from the microarrays were confirmed by the analysis of 12 genes included in the array by standard MSP and 3 out of 12 genes by pyrosequencing (Figure S3 and S4).
The results of microarrays were confirmed using real-time PCR.
In the FO-8 group, gene expression results by microarrays were confirmed by qPCR (88%).
Expression profiles for three genes identified with microarrays were confirmed with qRT-PCR.
Data generated from microarrays were confirmed using real-time PCR (qPCR).
Once the preprocessing step is complete, any differences between the microarrays are confirmed to be due to differential expression rather than printing, hybridization, or scanning artefacts.
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microarrays was reproduced
microarrays was imaged
microarrays was harvested
microarrays was evaluated
microarrays was obtained
microarrays was shown
microarrays was processed
microarrays was illustrated
microarrays was tested
microarrays was estimated
microarrays was prepared
microarrays was used
microarrays was carried
microarrays was adjusted
microarrays was done
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