That need for validation by the market is so destructive.
We selected a subset of genes for validation by qPCR.
106 SNPs and 30 indels detected in this study were selected for validation by Sanger sequencing.
Ten genes were selected for validation by quantitative real-time RT-PCR (qPCR).
Large contig sequences from the two air libraries were selected for validation by semi-quantitative PCR.
Nine genes of functional interest were selected for validation by quantitative PCR (qPCR) analysis (Table 2).
We selected two genes from bicluster9 for validation by qPCR at P13.
We randomly selected 14 novel miRNAs candidates for validation by qPCR.
We randomly selected 15 DEGs identified by microarray for validation by quantitative Real Time PCR (qRT-PCR).
It also produces a shorter list of candidates for validation by luciferase activity assays and transfection experiments.
Additionally, we selected four genes in three of the GSEA categories for validation by qPCR at P13 (Fig. 5C).
