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. 2015 Oct 29;65(3):367–393. doi: 10.1111/rssc.12126

Table 2.

Number of genes interacting with cdc13‐1 at 27C identified by using each of four approaches: Addinall et al. (2011) and the REM, IHM and JHMa

Method Suppressors Enhancers Hits Suppressors (half‐data) Enhancers (half‐data) Hits (half‐data) Telomere maintenance (N=33) p‐value q‐value Aging (N=58) p‐value q‐value Response to DNA damage stimulus (N=58) p‐value q‐value Peroxisome organization (N=180) p‐value q‐value
Addinall et al. (2011) 419 296 715 263 192 455 18
1.52×106
0.0376 16
4.32×105
0.1863 69
9.28×1012
8.14×1010
13 0.225 0.468
REM 184 131 315 103 86 189 11
2.37×105
0.0136 10 0.0004 0.0824 49
7.40×1016
1.73×1013
3 0.855 0.914
IHM 404 172 576 252 113 365 14
6.57×105
0.0051 16 0.0015 0.0445 55
4.60×109
3.41×107
10 0.318 0.524
JHM 665 274 939 475 177 601 18
8.22×105
0.0155 21 0.0015 0.0986 76
3.52×109
1.99×107
24 0.002 0.019
a

Number of genes classified (or annotated) with four example gene ontology terms (telomere maintenance, aging, response to DNA damage stimulus and peroxisome organization) are also listed. For the approach of Addinall et al. (2011) and REM, significant interactors are classified as those with false discovery rate corrected p‐values (or q‐values) less than 0.05. The label ‘half‐data’ denotes analyses where only half of the available experimental observations are used.