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. 2016 Mar 30;6(1):109–117. doi: 10.3233/JPD-150737

Table 2.

Quantitative real time PCR (qRT-PCR) validation of RNA-seq data

Official gene RNA Type Log2 FC Log2FC p-value p-value
symbol qRT-PCR RNA-seq qRT-PCR RNA-seq
UBC protein_coding 4.8 0.37 0.01 0.16
SSTR5 protein_coding –2.06 –2.27 0.02 2.3E-08
MAPK11 protein_coding –1.09 2.20 0.5 5.26E-12
PTPRC protein_coding –1.75 –1.84 0.18 9.37E-09
PARK7 protein_coding –1.97 0.14 0.17 0.99
NDUFV2 protein_coding –0.76 –2.22 0.06 2.73E-12
LRRK2 protein_coding –2.01 –0.1 0.33 0.49
LPAR1 protein_coding –1.23 –1.74 0.14 2.32E-08
EZH2 protein_coding 2.29 1.72 0.03 3.32E-06
DNMT1 protein_coding –1.38 1.14 0.01 0.000255726
CCR3 protein_coding –1.2 –4.47 0.05 1.34E-30
BMP7 protein_coding –1.84 –2.79 0.01 1.68E-29
AL356309.1 miRNA 0.37 –2.62 0.72 1.35E-13
AC010127.3 antisense –1.52 –2.31 0.08 3.81E-12
RP3-467N11.1 antisense –0.95 –3.24 0.56 9.08E-18
RP5-1051H14.2 lincRNA 1.36 2.68 0.4 1.5E-12
CTD-2066L21.2 lincRNA –1.2 –2.7 0.13 4.03E-14

We successfully confirmed the results of RNA-seq by qRT-PCR validation; the trend of fold changes (FC) in the two groups showed a 76% correlation between RNA-seq and qRT-PCR findings. Log2 fold changes (Log2FC) in qRT-PCR correlated with Log2FC in RNA-seq (p = 0.01, r2 = 0.65). The qRT-PCR and RNA-seq fold changes for four genes: PARK7, DNMT1, MAPK11 and AL356309.2 were not validated.