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. 2017 Apr 24;114(19):4981–4986. doi: 10.1073/pnas.1619523114

Fig. 6.

Fig. 6.

A subset of genes differentially expressed by RNA-sequencing were chosen to be validated by qPCR. RNAs from the same samples used for sequencing were reverse-transcribed and used to validate differential expression via the higher sensitivity TaqMan qPCR assay. Most of the validated genes showed more robust fold change values by qPCR than indicated by RNA-seq analysis. Error bars represent SEM.