Figure 1From: High-throughput identification of reference genes for research and clinical RT-qPCR analysis of breast cancer samplesEvaluation of candidate reference gene expression stability by RT-qPCR. Gene expression variations calculated for aggregated set of samples by a: comparative ΔCt (MΔCt); b: geNorm (MgeNorm) and d: NormFinder (MNormFinder). c: Maximum fold changes of gene expression levels MHaller calculated by Haller equivalence test.Back to article page