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. Author manuscript; available in PMC: 2017 Dec 15.
Published in final edited form as: DNA Repair (Amst). 2017 Jun 29;57:76–90. doi: 10.1016/j.dnarep.2017.06.028

Table 1.

Summary of genes analyzed by high-throughput RNA sequencing (RNA-Seq) and significant XPA-related differences.

Cell lines (XPA− vs. XPA+) Genes Analyzed FDR 0.05 (High + Low) FC ≥ 1.5 (High + Low)
XP2OS vs. XPA/XP2OS 14117 9526 1721 + 2206
XP12RO vs. XPA/XP12RO 13669 10283 2750 + 2625
KO38 vs. HeLa S3 14564 9520 1769 + 1701
KO142 vs. HeLa S3 13824 8364 1642 + 1422
Common genes 12022 176 + 149 11 + 16

The first column shows the number of genes analyzable by RNA-Seq for each XPA-proficient/deficient cell pair. The second column shows the number of genes with differential expression at a False Discovery Rate (FDR) of 0.05. The ratio of gene expression was calculated for XPA+/XPA− for each cell pair; positive log 2 values are termed “high” and negative log 2 values are termed “low”. The third column shows for each cell pair the number of “high” or “low” genes with fold change (FC) of 1.5 or more.