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. 2016 Apr 8;7:486. doi: 10.3389/fpls.2016.00486

Table 1.

Pearson correlation analysis of gene expression values detected by RNA sequencing and qPCR.

Genes Methods 45 DPA 142 DPA Pcc p-value


Newhall Xinhui Bingtang Succari Newhall Xinhui Bingtang Succari
Cs1g16150 RNA seq 5.0 0.8 0.4 0.0 40.2 30.4 7.7 0.0 0.98 2.8E-05
(AHA10) qPCR 1.0 0.2 0.1 0.0 17.0 10.3 5.7 0.0
Cs1g20480 RNA seq 9.9 10.7 14.4 11.8 1.1 0.6 0.8 13.1 0.99 4.3E-06
(AIL6) qPCR 1.0 1.2 1.4 1.2 0.1 0.1 0.1 2.0
Cs5g31400 RNA seq 2.3 1.3 0.9 0.5 30.7 14.1 6.3 2.4 0.98 1.7E-05
(TT8) qPCR 1.0 0.8 0.5 0.1 22.6 6.5 4.2 1.1
Cs6g08410 RNA seq 1.0 0.7 0.6 0.5 11.2 6.9 2.1 0.5 0.94 5.8E-04
(APD2) qPCR 1.0 0.6 0.5 0.7 29.8 19.0 11.7 1.3
Cs9g17580 RNA seq 0.5 0.3 0.1 0.1 8.2 3.4 1.4 0.1 0.94 5.8E-04
(unknown) qPCR 1.0 0.7 0.4 0.7 12.7 6.2 2.6 0.1
Cs6g15800 RNA seq 0.7 1.4 1.2 1.8 5.2 13.3 21.8 26.0 0.99 4.2E-06
(glycosyltransferase) qPCR 1.0 2.3 1.3 2.0 6.2 20.3 20.6 45.9
Cs1g25820 RNA seq 0.0 0.0 0.2 0.0 2.2 0.2 0.8 18.7 0.98 1.5E-05
(Heavy metal-associated domain containing protein) qPCR 1.0 1.1 0.9 2.1 10.2 3.1 6.2 135.6

Expression patterns for seven genes which were determined to be differentially regulated between different varieties by RNA sequencing (RNA seq) were validated by using quantitative PCR (qPCR) analysis of the RT products. Values are the means of RNA seq data (RPKM) or qPCR data (with the value for Newhall at 45 DPA set as 1 after normalization to the Actin control) from three biological replicates. DPA, days post anthesis; Pcc, Pearson correlation coefficient.