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Microarray data were validated by quantitative polymerase chain reaction.
The microarray data were validated by quantitative PCR (qPCR) on a subset of 10 genes.
Kramers Kronig transformation implied that the resulting impedance data were validated and were of very good quality.
RNA-seq data were validated using the RT-PCR and qRT-PCR; the level of AS of these SR genes was estimated using isoform-specific primers in each case (Supplementary Table S5, Supplementary Figure S6).
The subjects' data were validated.
Data were validated by immunohistology.
The data were validated with the Epi Info v.6.4 program.
Before running the Heckman selection model, data were validated for multicollinearity and heteroskedasticity.
These compiled data were validated and cross-checked with each set to ensure it is representative of those scenarios considered.
The net CSOR data were validated using the theory of gravity drainage and its application in the SAGD process.
The microarray data were validated by qPCR.
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