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The large number of significantly upregulated LINE-1 probes in the Tex19.1 −/− placenta microarray data prompted us to look more closely at LINE-1 expression in this tissue.
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The growing amount of publicly available microarray data has prompted researchers to explore ways to compare results between experiments across the different platforms.
These data prompted us to carry out a more detailed characterization of the epitopes recognized by the two mAbs using microarray analyses.
Answer "yes" to "Erase all data" prompt.
The dramatic enrichment of class 2 nTEs around genes especially in promoters prompted us to analyze the correlation between these elements and nearby gene expression levels using microarray data.
TK and RNI analyzed the microarray data.
Thus, understanding microarray data processing steps becomes critical for performing optimal microarray data analysis.
Steps 3.3 and 3.4 extracted drug microarray and disease microarray data respectively.
Fig. 2 Validation of microarray data by quantitative RT-PCR.
The center panels display light vs. dark NSF45K microarray data.
The accession number of the microarray data was GSE73814.
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