Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 824 | vesicle transport | 0.18 | 9 | e--7 | 2 | 95 | vesicle transport(p=-7.073963,f=0.18,n=9,id=GO:0016192) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1003 | urea cycle intermediate metabolism | 0.142 | 4 | e--9 | 34 | 58 | amino acid biosynthesis(p=-26.498969,f=0.392,n=11,id=GO:0008652) | TGACTCA | -15.161 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 2014 | ubiquitin-dependent protein degradation | 0.705 | 12 | e--35 | 55 | 19 | ubiquitin-dependent protein degradation(p=-35.162253,f=0.705,n=12,id=GO:0006511) | GTGGCAAA | -14.8233 |
Mod 1168 | ubiquitin-dependent protein degradation | 0.7 | 21 | e--64 | 65 | 40 | ubiquitin-dependent protein degradation(p=-64.378155,f=0.7,n=21,id=GO:0006511) | GGTGGC | -24.2364 |
Mod 2795 | ubiquitin-dependent protein degradation | 0.366 | 22 | e--48 | 53 | 87 | ubiquitin-dependent protein degradation(p=-48.183607,f=0.366,n=22,id=GO:0006511) | GGTGGC | -20.1839 |
Mod 982 | ubiquitin-dependent protein degradation | 0.271 | 31 | e--60 | 64 | 184 | ubiquitin-dependent protein degradation(p=-60.023724,f=0.271,n=31,id=GO:0006511) | AAGGGG | -20.3047 |
Mod 2780 | ubiquitin-dependent protein degradation | 0.126 | 34 | e--40 | 16 | 440 | proteolysis and peptidolysis(p=-43.379669,f=0.144,n=39,id=GO:0006508) | GTGGCAA | -18.8322 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1093 | tryptophan biosynthesis | 0.235 | 4 | e--13 | 58 | 25 | tryptophan biosynthesis(p=-13.480959,f=0.235,n=4,id=GO:0000162) | TGACTCA | -13.9284 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 2077 | tricarboxylic acid cycle | 0.275 | 8 | e--29 | 63 | 45 | tricarboxylic acid cycle(p=-29.157554,f=0.275,n=8,id=GO:0006099) | CGG7CAA | -12.1457 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1059 | translational fidelity | 0.12 | 3 | e--8 | 147 | 28 | protein biosynthesis(p=-36.336656,f=0.72,n=18,id=GO:0006412) | ||
Mod 2467 | translational fidelity | 0.111 | 4 | e--12 | 157 | 40 | protein biosynthesis(p=-46.314331,f=0.666,n=24,id=GO:0006412) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 2967 | transcription\, from Pol II promoter | 0.204 | 9 | e--13 | 18 | 69 | transcription\, DNA-dependent(p=-21.641654,f=0.409,n=18,id=GO:0006351) | ||
Mod 2796 | transcription\, from Pol II promoter | 0.136 | 26 | e--33 | 16 | 289 | transcription\, from Pol II promoter(p=-33.987739,f=0.136,n=26,id=GO:0006366) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1808 | transcription\, from Pol I promoter | 0.785 | 11 | e--36 | 187 | 30 | transcription\, from Pol I promoter(p=-36.086249,f=0.785,n=11,id=GO:0006360) | GATGAG | -16.4503 |
Mod 911 | transcription\, from Pol I promoter | 0.483 | 43 | e--126 | 180 | 185 | ribosome biogenesis(p=-144.589732,f=0.561,n=50,id=GO:0007046) | GATGAG | -84.8431 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 2697 | transcription\, DNA-dependent | 0.666 | 10 | e--17 | 153 | 29 | transcription\, DNA-dependent(p=-17.507404,f=0.666,n=10,id=GO:0006351) | AAAATT | -18.5566 |
Mod 2967 | transcription\, DNA-dependent | 0.409 | 18 | e--21 | 18 | 69 | transcription\, DNA-dependent(p=-21.641654,f=0.409,n=18,id=GO:0006351) | ||
Mod 2796 | transcription\, DNA-dependent | 0.193 | 37 | e--20 | 16 | 289 | transcription\, from Pol II promoter(p=-33.987739,f=0.136,n=26,id=GO:0006366) | ||
Mod 2780 | transcription\, DNA-dependent | 0.141 | 38 | e--12 | 16 | 440 | proteolysis and peptidolysis(p=-43.379669,f=0.144,n=39,id=GO:0006508) | GTGGCAA | -18.8322 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 3226 | transcription regulation\, from Pol II promoter | 1 | 4 | e--10 | 65 | 6 | mating-type specific transcriptional control(p=-21.85784,f=1,n=4,id=GO:0007532) | ||
Mod 2967 | transcription regulation\, from Pol II promoter | 0.181 | 8 | e--9 | 18 | 69 | transcription\, DNA-dependent(p=-21.641654,f=0.409,n=18,id=GO:0006351) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 913 | transcription initiation\, from Pol II promoter | 0.17 | 7 | e--13 | 19 | 59 | transcription initiation\, from Pol II promoter(p=-13.592135,f=0.17,n=7,id=GO:0006367) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1481 | sulfur amino acid metabolism | 0.75 | 3 | e--9 | 122 | 5 | sulfur amino acid metabolism(p=-9.900741,f=0.75,n=3,id=GO:0000096) | ||
Mod 1088 | sulfur amino acid metabolism | 0.134 | 7 | e--14 | 26 | 72 | amino acid metabolism(p=-44.173355,f=0.403,n=21,id=GO:0006520) | GATAAG | -25.384 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 3133 | sulfur amino acid biosynthesis | 0.235 | 4 | e--14 | 100 | 26 | sulfate assimilation(p=-35.182758,f=0.411,n=7,id=GO:0000103) | CACGTG | -20.1247 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 3131 | sulfate assimilation | 0.461 | 6 | e--29 | 126 | 18 | sulfate assimilation(p=-29.070438,f=0.461,n=6,id=GO:0000103) | CACGTG | -12.2311 |
Mod 3133 | sulfate assimilation | 0.411 | 7 | e--35 | 100 | 26 | sulfate assimilation(p=-35.182758,f=0.411,n=7,id=GO:0000103) | CACGTG | -20.1247 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 53 | stress response | 0.666 | 4 | e--8 | 177 | 11 | stress response(p=-8.362051,f=0.666,n=4,id=GO:0006950) | GGC5GGC | -15.6782 |
Mod 43 | stress response | 0.545 | 6 | e--11 | 118 | 13 | protein folding(p=-24.131792,f=0.636,n=7,id=GO:0006457) | TTCTAGAA | -14.209 |
Mod 3111 | stress response | 0.483 | 15 | e--30 | 122 | 48 | protein folding(p=-46.531554,f=0.451,n=14,id=GO:0006457) | GGGGCG | -17.2079 |
Mod 1087 | stress response | 0.263 | 24 | e--34 | 157 | 186 | stress response(p=-34.175841,f=0.263,n=24,id=GO:0006950) | AAGGGG | -64.6463 |
Mod 982 | stress response | 0.219 | 25 | e--31 | 64 | 184 | ubiquitin-dependent protein degradation(p=-60.023724,f=0.271,n=31,id=GO:0006511) | AAGGGG | -20.3047 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 144 | sterol metabolism | 0.5 | 8 | e--27 | 27 | 38 | ergosterol metabolism(p=-19.00217,f=0.375,n=6,id=GO:0008204) | TA1ACGA | -13.8446 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 2194 | steroid biosynthesis | 1 | 3 | e--9 | 92 | 3 | ergosterol metabolism(p=-10.130896,f=1,n=3,id=GO:0008204) | ||
Mod 1146 | steroid biosynthesis | 0.857 | 6 | e--24 | 62 | 10 | ergosterol metabolism(p=-26.574879,f=0.857,n=6,id=GO:0008204) | CCGATA | -13.3525 |
Mod 145 | steroid biosynthesis | 0.518 | 14 | e--52 | 24 | 35 | ergosterol metabolism(p=-52.109587,f=0.481,n=13,id=GO:0008204) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1726 | starvation response | 0.666 | 4 | e--17 | 118 | 7 | asparagine metabolism(p=-20.373615,f=0.666,n=4,id=GO:0006528) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1170 | sporulation (sensu Saccharomyces) | 0.75 | 3 | e--8 | 44 | 12 | sporulation (sensu Saccharomyces)(p=-8.502497,f=0.75,n=3,id=GO:0007151) | CTTGGC | -13.0152 |
Mod 544 | sporulation (sensu Saccharomyces) | 0.666 | 4 | e--11 | 31 | 14 | sporulation (sensu Saccharomyces)(p=-11.33851,f=0.666,n=4,id=GO:0007151) | ||
Mod 3230 | sporulation (sensu Saccharomyces) | 0.52 | 13 | e--39 | 27 | 53 | sporulation (sensu Saccharomyces)(p=-39.678845,f=0.52,n=13,id=GO:0007151) | CACAAA | -14.38 |
Mod 2974 | sporulation (sensu Saccharomyces) | 0.176 | 27 | e--56 | 13 | 247 | nuclear division(p=-83.02673,f=0.333,n=51,id=GO:0000280) | CACAAA | -47.4602 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 206 | sporulation (sensu Fungi) | 0.75 | 3 | e--8 | 42 | 30 | sporulation (sensu Fungi)(p=-8.311369,f=0.75,n=3,id=GO:0030437) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 70 | spore wall assembly (sensu Saccharomyces) | 0.571 | 4 | e--13 | 43 | 22 | spore wall assembly (sensu Saccharomyces)(p=-13.813362,f=0.571,n=4,id=GO:0007152) | ||
Mod 3230 | spore wall assembly (sensu Saccharomyces) | 0.36 | 9 | e--31 | 27 | 53 | sporulation (sensu Saccharomyces)(p=-39.678845,f=0.52,n=13,id=GO:0007151) | CACAAA | -14.38 |
Mod 2974 | spore wall assembly (sensu Saccharomyces) | 0.117 | 18 | e--53 | 13 | 247 | nuclear division(p=-83.02673,f=0.333,n=51,id=GO:0000280) | CACAAA | -47.4602 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 591 | spore wall assembly (sensu Fungi) | 0.75 | 3 | e--10 | 56 | 8 | spore wall assembly (sensu Fungi)(p=-10.627441,f=0.75,n=3,id=GO:0030476) | ||
Mod 1174 | spore wall assembly (sensu Fungi) | 0.571 | 4 | e--13 | 53 | 14 | spore wall assembly (sensu Saccharomyces)(p=-8.43449,f=0.428,n=3,id=GO:0007152) | ||
Mod 204 | spore wall assembly (sensu Fungi) | 0.294 | 5 | e--14 | 46 | 33 | spore wall assembly (sensu Saccharomyces)(p=-10.02638,f=0.235,n=4,id=GO:0007152) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 920 | signal transduction | 0.103 | 15 | e--11 | 2 | 268 | autophagy(p=-12.902251,f=0.055,n=8,id=GO:0006914) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 26 | serine family amino acid biosynthesis | 0.25 | 3 | e--10 | 150 | 13 | one-carbon compound metabolism(p=-13.581448,f=0.333,n=4,id=GO:0006730) | TGACTC | -22.4281 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 28 | ribosome biogenesis | 0.75 | 3 | e--7 | 228 | 9 | transcription\, from Pol I promoter(p=-7.73596,f=0.75,n=3,id=GO:0006360) | ||
Mod 3040 | ribosome biogenesis | 0.666 | 6 | e--15 | 154 | 19 | transcription\, from Pol I promoter(p=-16.510518,f=0.666,n=6,id=GO:0006360) | AAAATTT | -14.2696 |
Mod 911 | ribosome biogenesis | 0.561 | 50 | e--144 | 180 | 185 | ribosome biogenesis(p=-144.589732,f=0.561,n=50,id=GO:0007046) | GATGAG | -84.8431 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 2467 | ribosomal small subunit assembly and maintenance | 0.111 | 4 | e--9 | 157 | 40 | protein biosynthesis(p=-46.314331,f=0.666,n=24,id=GO:0006412) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 3025 | ribosomal large subunit assembly and maintenance | 0.6 | 3 | e--8 | 179 | 10 | ribosomal large subunit assembly and maintenance(p=-8.807078,f=0.6,n=3,id=GO:0000027) | GCC9AGC | -11.5407 |
Mod 1127 | ribosomal large subunit assembly and maintenance | 0.25 | 4 | e--8 | 197 | 42 | transcription\, from Pol I promoter(p=-23.945101,f=0.562,n=9,id=GO:0006360) | AAATTT | -24.7786 |
Mod 2663 | ribosomal large subunit assembly and maintenance | 0.227 | 5 | e--11 | 183 | 47 | RNA processing(p=-23.033189,f=0.545,n=12,id=GO:0006396) | GATGAG | -26.1875 |
Mod 1870 | ribosomal large subunit assembly and maintenance | 0.175 | 7 | e--15 | 180 | 42 | protein biosynthesis(p=-103.582413,f=0.95,n=38,id=GO:0006412) | TCC3CAT | -15.3083 |
Mod 911 | ribosomal large subunit assembly and maintenance | 0.157 | 14 | e--34 | 180 | 185 | ribosome biogenesis(p=-144.589732,f=0.561,n=50,id=GO:0007046) | GATGAG | -84.8431 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1175 | response to external stimulus | 0.24 | 12 | e--10 | 1 | 102 | response to external stimulus(p=-10.035725,f=0.24,n=12,id=GO:0009605) | ||
Mod 1006 | response to external stimulus | 0.2 | 15 | e--10 | 5 | 124 | amino acid metabolism(p=-12.515916,f=0.16,n=12,id=GO:0006520) | ||
Mod 1079 | response to external stimulus | 0.147 | 17 | e--8 | 2 | 206 | methionine and threonine metabolism(p=-6.115813,f=0.043,n=5,id=GO:0018927) | ||
Mod 3269 | response to external stimulus | 0.12 | 21 | e--7 | 0 | 326 | protein modification(p=-24.983008,f=0.188,n=33,id=GO:0006464) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1754 | response to biotic stimulus | 0.5 | 4 | e--7 | 104 | 12 | non-covalent chromatin modification(p=-5.770431,f=0.375,n=3,id=GO:0016582) | ||
Mod 1240 | response to biotic stimulus | 0.144 | 10 | e--10 | 27 | 122 | stress response(p=-15.169032,f=0.202,n=14,id=GO:0006950) | CCCCCT | -12.4291 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1363 | response to abiotic stimulus | 0.666 | 4 | e--8 | 11 | 12 | response to abiotic stimulus(p=-8.670479,f=0.666,n=4,id=GO:0009628) | ||
Mod 839 | response to abiotic stimulus | 0.208 | 10 | e--11 | 2 | 109 | response to abiotic stimulus(p=-11.392006,f=0.208,n=10,id=GO:0009628) | ||
Mod 1975 | response to abiotic stimulus | 0.203 | 12 | e--13 | 51 | 93 | mating (sensu Saccharomyces)(p=-79.978314,f=0.491,n=29,id=GO:0007322) | TGAAAC | -25.2808 |
Mod 3262 | response to abiotic stimulus | 0.187 | 18 | e--20 | 0 | 146 | amino acid metabolism(p=-91.502909,f=0.416,n=40,id=GO:0006520) | TGACTC | -14.1346 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 911 | rRNA processing | 0.404 | 36 | e--109 | 180 | 185 | ribosome biogenesis(p=-144.589732,f=0.561,n=50,id=GO:0007046) | GATGAG | -84.8431 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 2386 | rRNA modification | 0.375 | 3 | e--8 | 231 | 12 | rRNA modification(p=-8.916606,f=0.375,n=3,id=GO:0000154) | ||
Mod 1808 | rRNA modification | 0.285 | 4 | e--12 | 187 | 30 | transcription\, from Pol I promoter(p=-36.086249,f=0.785,n=11,id=GO:0006360) | GATGAG | -16.4503 |
Mod 1807 | rRNA modification | 0.125 | 5 | e--12 | 151 | 67 | transcription\, from Pol I promoter(p=-34.587673,f=0.375,n=15,id=GO:0006360) | AATTTT | -25.6582 |
Mod 911 | rRNA modification | 0.123 | 11 | e--34 | 180 | 185 | ribosome biogenesis(p=-144.589732,f=0.561,n=50,id=GO:0007046) | GATGAG | -84.8431 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 3093 | pyruvate metabolism | 0.272 | 3 | e--9 | 147 | 12 | glucose metabolism(p=-31.439676,f=0.727,n=8,id=GO:0006006) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 3059 | pyridoxine metabolism | 0.666 | 4 | e--20 | 63 | 7 | pyridoxine metabolism(p=-20.373615,f=0.666,n=4,id=GO:0008614) | ||
Mod 652 | pyridoxine metabolism | 0.176 | 6 | e--25 | 23 | 69 | pyridoxine metabolism(p=-25.391885,f=0.176,n=6,id=GO:0008614) | AGGCAC | -13.5304 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1830 | purine nucleotide biosynthesis | 0.3 | 3 | e--8 | 121 | 11 | purine nucleoside monophosphate metabolism(p=-9.315079,f=0.3,n=3,id=GO:0009126) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1830 | purine nucleoside monophosphate metabolism | 0.3 | 3 | e--9 | 121 | 11 | purine nucleoside monophosphate metabolism(p=-9.315079,f=0.3,n=3,id=GO:0009126) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 2568 | purine base metabolism | 0.428 | 3 | e--9 | 52 | 11 | purine base metabolism(p=-9.024139,f=0.428,n=3,id=GO:0006144) | CTTATC | -13.2522 |
Mod 1089 | purine base metabolism | 0.307 | 4 | e--11 | 61 | 22 | purine base metabolism(p=-11.939233,f=0.307,n=4,id=GO:0006144) | ||
Mod 3069 | purine base metabolism | 0.233 | 7 | e--22 | 100 | 35 | amino acid metabolism(p=-51.03999,f=0.633,n=19,id=GO:0006520) | TGACTC | -45.2792 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 2780 | proteolysis and peptidolysis | 0.144 | 39 | e--43 | 16 | 440 | proteolysis and peptidolysis(p=-43.379669,f=0.144,n=39,id=GO:0006508) | GTGGCAA | -18.8322 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 3105 | protein-vacuolar targeting | 0.25 | 7 | e--14 | 0 | 52 | autophagy(p=-20.508202,f=0.25,n=7,id=GO:0006914) | ||
Mod 3273 | protein-vacuolar targeting | 0.112 | 11 | e--16 | 0 | 180 | protein-vacuolar targeting(p=-16.479507,f=0.112,n=11,id=GO:0006623) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1555 | protein-nucleus import | 0.5 | 3 | e--7 | 20 | 8 | protein-nucleus import(p=-7.442298,f=0.5,n=3,id=GO:0006606) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 2922 | protein-nucleus export | 0.16 | 4 | e--7 | 11 | 29 | protein-nucleus export(p=-7.264773,f=0.16,n=4,id=GO:0006611) | ||
Mod 638 | protein-nucleus export | 0.1 | 6 | e--9 | 17 | 105 | protein-nucleus export(p=-9.70406,f=0.1,n=6,id=GO:0006611) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 638 | protein targeting | 0.166 | 10 | e--8 | 17 | 105 | protein-nucleus export(p=-9.70406,f=0.1,n=6,id=GO:0006611) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 2473 | protein synthesis initiation | 0.312 | 5 | e--13 | 90 | 21 | protein synthesis initiation(p=-13.21455,f=0.312,n=5,id=GO:0006413) | ||
Mod 1206 | protein synthesis initiation | 0.145 | 7 | e--14 | 122 | 73 | protein biosynthesis(p=-45.791349,f=0.562,n=27,id=GO:0006412) | AAATTT | -22.4499 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 112 | protein synthesis elongation | 0.3 | 3 | e--8 | 168 | 10 | protein biosynthesis(p=-25.532505,f=1,n=10,id=GO:0006412) | CCTTCTA | -13.3018 |
Mod 2902 | protein synthesis elongation | 0.162 | 6 | e--16 | 108 | 43 | protein biosynthesis(p=-20.849203,f=0.432,n=16,id=GO:0006412) | GAA4TTT | -16.0814 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1329 | protein modification | 0.8 | 4 | e--8 | 43 | 9 | protein modification(p=-8.451915,f=0.8,n=4,id=GO:0006464) | ||
Mod 1100 | protein modification | 0.261 | 11 | e--10 | 8 | 74 | protein modification(p=-10.261952,f=0.261,n=11,id=GO:0006464) | ||
Mod 2726 | protein modification | 0.23 | 15 | e--12 | 14 | 112 | protein modification(p=-12.836236,f=0.23,n=15,id=GO:0006464) | ||
Mod 3269 | protein modification | 0.188 | 33 | e--24 | 0 | 326 | protein modification(p=-24.983008,f=0.188,n=33,id=GO:0006464) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 43 | protein folding | 0.636 | 7 | e--24 | 118 | 13 | protein folding(p=-24.131792,f=0.636,n=7,id=GO:0006457) | TTCTAGAA | -14.209 |
Mod 3111 | protein folding | 0.451 | 14 | e--46 | 122 | 48 | protein folding(p=-46.531554,f=0.451,n=14,id=GO:0006457) | GGGGCG | -17.2079 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 696 | protein complex assembly | 0.6 | 3 | e--8 | 73 | 7 | protein complex assembly(p=-8.946845,f=0.6,n=3,id=GO:0006461) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1766 | protein biosynthesis | 1 | 38 | e--109 | 187 | 42 | protein biosynthesis(p=-109.734081,f=1,n=38,id=GO:0006412) | CC2ACAT | -20.6462 |
Mod 1179 | protein biosynthesis | 0.976 | 42 | e--119 | 173 | 45 | protein biosynthesis(p=-119.311981,f=0.976,n=42,id=GO:0006412) | CC2ACAT | -21.0441 |
Mod 981 | protein biosynthesis | 0.789 | 135 | e--338 | 153 | 209 | protein biosynthesis(p=-338.315184,f=0.789,n=135,id=GO:0006412) | CCGTAC | -21.843 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1048 | protein amino acid glycosylation | 0.105 | 8 | e--10 | 12 | 105 | protein amino acid glycosylation(p=-10.053174,f=0.105,n=8,id=GO:0006486) | CAC9CTT | -11.4683 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 663 | pre-replicative complex formation and maintenance | 0.25 | 3 | e--8 | 85 | 16 | pre-replicative complex formation and maintenance(p=-8.593229,f=0.25,n=3,id=GO:0006267) | ||
Mod 1067 | pre-replicative complex formation and maintenance | 0.138 | 5 | e--14 | 39 | 50 | pre-replicative complex formation and maintenance(p=-14.600786,f=0.138,n=5,id=GO:0006267) | CC6GGAA | -16.6593 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 927 | post-replication repair | 0.214 | 3 | e--9 | 35 | 22 | DNA strand elongation(p=-6.204268,f=0.214,n=3,id=GO:0006271) | ACGCGT | -13.7868 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 724 | post Golgi transport | 1 | 3 | e--9 | 68 | 3 | post Golgi transport(p=-9.004992,f=1,n=3,id=GO:0006892) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 840 | porphyrin biosynthesis | 0.21 | 4 | e--8 | 63 | 29 | hexose transport(p=-18.651663,f=0.315,n=6,id=GO:0008645) | AGGCAC | -13.4549 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 895 | phosphorylation | 0.32 | 8 | e--15 | 108 | 29 | phosphorylation(p=-15.696222,f=0.32,n=8,id=GO:0016310) | GGGGGC | -11.5413 |
Mod 1103 | phosphorylation | 0.214 | 12 | e--20 | 83 | 76 | energy derivation by oxidation of organic compounds(p=-60.191008,f=0.482,n=27,id=GO:0015980) | CCAATC | -18.3177 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 721 | phosphatidylcholine biosynthesis | 0.19 | 4 | e--13 | 46 | 27 | phosphatidylcholine biosynthesis(p=-13.975369,f=0.19,n=4,id=GO:0006656) | CATGTG | -14.6635 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1823 | pheromone response | 0.5 | 3 | e--7 | 78 | 10 | mating (sensu Saccharomyces)(p=-9.98488,f=0.666,n=4,id=GO:0007322) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 2227 | pheromone response (sensu Fungi) | 0.5 | 6 | e--19 | 137 | 13 | pheromone response (sensu Fungi)(p=-19.450581,f=0.5,n=6,id=GO:0030434) | ||
Mod 1975 | pheromone response (sensu Fungi) | 0.135 | 8 | e--16 | 51 | 93 | mating (sensu Saccharomyces)(p=-79.978314,f=0.491,n=29,id=GO:0007322) | TGAAAC | -25.2808 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 3245 | oxidative stress response | 0.24 | 6 | e--15 | 58 | 49 | aldehyde metabolism(p=-22.559253,f=0.24,n=6,id=GO:0006081) | TTACTAA | -13.4903 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 3057 | ornithine metabolism | 0.266 | 4 | e--16 | 148 | 16 | amino acid biosynthesis(p=-48.053881,f=0.866,n=13,id=GO:0008652) | TGACTC | -39.5394 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 27 | one-carbon compound metabolism | 0.666 | 4 | e--16 | 187 | 6 | one-carbon compound metabolism(p=-16.974462,f=0.666,n=4,id=GO:0006730) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1457 | nucleotide metabolism | 0.75 | 3 | e--10 | 162 | 5 | nucleotide metabolism(p=-10.832543,f=0.75,n=3,id=GO:0009117) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 2895 | nuclear division | 0.55 | 11 | e--21 | 17 | 28 | nuclear division(p=-21.688498,f=0.55,n=11,id=GO:0000280) | ||
Mod 2974 | nuclear division | 0.333 | 51 | e--83 | 13 | 247 | nuclear division(p=-83.02673,f=0.333,n=51,id=GO:0000280) | CACAAA | -47.4602 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1555 | nuclear RNA-nucleus export | 0.5 | 3 | e--7 | 20 | 8 | protein-nucleus import(p=-7.442298,f=0.5,n=3,id=GO:0006606) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 2703 | non-selective vesicle fusion | 0.114 | 4 | e--7 | 24 | 53 | exocytosis(p=-10.203844,f=0.228,n=8,id=GO:0006887) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 167 | nitrogen metabolism | 0.333 | 3 | e--7 | 57 | 14 | mating-type specific transcriptional control(p=-11.137922,f=0.333,n=3,id=GO:0007532) | TAG4GAG | -11.4422 |
Mod 1088 | nitrogen metabolism | 0.173 | 9 | e--22 | 26 | 72 | amino acid metabolism(p=-44.173355,f=0.403,n=21,id=GO:0006520) | GATAAG | -25.384 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1488 | nicotinamide adenine dinucleotide metabolism | 1 | 4 | e--18 | 45 | 8 | nicotinamide adenine dinucleotide metabolism(p=-18.813318,f=1,n=4,id=GO:0019674) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1017 | monovalent inorganic cation transport | 0.5 | 3 | e--8 | 68 | 7 | monovalent inorganic cation transport(p=-8.942074,f=0.5,n=3,id=GO:0015672) | ||
Mod 1235 | monovalent inorganic cation transport | 0.16 | 4 | e--8 | 37 | 37 | catabolic carbohydrate metabolism(p=-12.921055,f=0.24,n=6,id=GO:0006095) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1512 | mitotic prophase | 0.25 | 3 | e--7 | 13 | 23 | mitotic prophase(p=-7.050448,f=0.25,n=3,id=GO:0000088) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1169 | mitotic metaphase/anaphase transition | 0.1 | 5 | e--11 | 10 | 77 | spore wall assembly (sensu Saccharomyces)(p=-16.921709,f=0.14,n=7,id=GO:0007152) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 419 | mitotic cell cycle | 0.8 | 4 | e--8 | 135 | 12 | mitotic cell cycle(p=-8.500186,f=0.8,n=4,id=GO:0000278) | AC1CGAA | -11.9457 |
Mod 2632 | mitotic cell cycle | 0.714 | 5 | e--9 | 108 | 11 | mitotic cell cycle(p=-9.838298,f=0.714,n=5,id=GO:0000278) | ||
Mod 619 | mitotic cell cycle | 0.666 | 12 | e--24 | 69 | 29 | mitotic cell cycle(p=-24.681719,f=0.666,n=12,id=GO:0000278) | AACGCG | -13.6558 |
Mod 969 | mitotic cell cycle | 0.46 | 29 | e--48 | 58 | 92 | DNA metabolism(p=-58.77429,f=0.539,n=34,id=GO:0006259) | ACGCGT | -78.5011 |
Mod 2463 | mitotic cell cycle | 0.117 | 31 | e--12 | 14 | 464 | transcription\, from Pol II promoter(p=-13.168926,f=0.071,n=19,id=GO:0006366) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1169 | mitotic anaphase | 0.12 | 6 | e--10 | 10 | 77 | spore wall assembly (sensu Saccharomyces)(p=-16.921709,f=0.14,n=7,id=GO:0007152) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1510 | mitosis | 0.444 | 4 | e--7 | 11 | 17 | mitosis(p=-7.270573,f=0.444,n=4,id=GO:0007067) | ||
Mod 2895 | mitosis | 0.3 | 6 | e--9 | 17 | 28 | nuclear division(p=-21.688498,f=0.55,n=11,id=GO:0000280) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 2899 | mitochondrion organization and biogenesis | 0.146 | 6 | e--7 | 15 | 65 | flocculation(p=-7.590849,f=0.073,n=3,id=GO:0000128) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1113 | mitochondrial translocation | 0.21 | 4 | e--9 | 23 | 26 | mitochondrial translocation(p=-9.479151,f=0.21,n=4,id=GO:0006628) | ||
Mod 1711 | mitochondrial translocation | 0.161 | 5 | e--11 | 44 | 35 | mitochondrial translocation(p=-11.457425,f=0.161,n=5,id=GO:0006628) | CT6GGCG | -12.6629 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 738 | mismatch repair | 0.6 | 3 | e--9 | 68 | 8 | mismatch repair(p=-9.965326,f=0.6,n=3,id=GO:0006298) | ||
Mod 1219 | mismatch repair | 0.307 | 4 | e--11 | 74 | 14 | lagging strand elongation(p=-18.158463,f=0.384,n=5,id=GO:0006273) | ACGCGT | -24.383 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 2932 | microtubule nucleation | 0.208 | 5 | e--11 | 28 | 44 | microtubule nucleation(p=-11.121359,f=0.208,n=5,id=GO:0007020) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 3131 | methionine metabolism | 0.461 | 6 | e--21 | 126 | 18 | sulfate assimilation(p=-29.070438,f=0.461,n=6,id=GO:0000103) | CACGTG | -12.2311 |
Mod 3133 | methionine metabolism | 0.411 | 7 | e--25 | 100 | 26 | sulfate assimilation(p=-35.182758,f=0.411,n=7,id=GO:0000103) | CACGTG | -20.1247 |
Mod 3262 | methionine metabolism | 0.135 | 13 | e--38 | 0 | 146 | amino acid metabolism(p=-91.502909,f=0.416,n=40,id=GO:0006520) | TGACTC | -14.1346 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1017 | metal ion transport | 0.5 | 3 | e--7 | 68 | 7 | monovalent inorganic cation transport(p=-8.942074,f=0.5,n=3,id=GO:0015672) | ||
Mod 914 | metal ion transport | 0.195 | 8 | e--18 | 10 | 71 | copper ion transport(p=-14.032932,f=0.121,n=5,id=GO:0006825) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 859 | meiosis I | 0.375 | 3 | e--7 | 51 | 15 | meiosis I(p=-7.082974,f=0.375,n=3,id=GO:0007127) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 384 | meiosis | 1 | 3 | e--7 | 71 | 5 | meiosis(p=-7.414188,f=1,n=3,id=GO:0007126) | ||
Mod 544 | meiosis | 0.666 | 4 | e--10 | 31 | 14 | sporulation (sensu Saccharomyces)(p=-11.33851,f=0.666,n=4,id=GO:0007151) | ||
Mod 475 | meiosis | 0.555 | 5 | e--11 | 31 | 22 | meiosis(p=-11.990629,f=0.555,n=5,id=GO:0007126) | ||
Mod 904 | meiosis | 0.5 | 7 | e--16 | 26 | 26 | meiosis(p=-16.859603,f=0.5,n=7,id=GO:0007126) | ||
Mod 2974 | meiosis | 0.189 | 29 | e--50 | 13 | 247 | nuclear division(p=-83.02673,f=0.333,n=51,id=GO:0000280) | CACAAA | -47.4602 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 3226 | mating-type specific transcriptional control | 1 | 4 | e--21 | 65 | 6 | mating-type specific transcriptional control(p=-21.85784,f=1,n=4,id=GO:0007532) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 596 | mating (sensu Saccharomyces) | 0.833 | 5 | e--15 | 132 | 7 | mating (sensu Saccharomyces)(p=-15.234964,f=0.833,n=5,id=GO:0007322) | ||
Mod 1966 | mating (sensu Saccharomyces) | 0.615 | 8 | e--21 | 63 | 23 | mating (sensu Saccharomyces)(p=-21.50426,f=0.615,n=8,id=GO:0007322) | ATG4GTC | -12.3978 |
Mod 1975 | mating (sensu Saccharomyces) | 0.491 | 29 | e--79 | 51 | 93 | mating (sensu Saccharomyces)(p=-79.978314,f=0.491,n=29,id=GO:0007322) | TGAAAC | -25.2808 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 205 | mating (sensu Fungi) | 1 | 3 | e--7 | 62 | 17 | mating (sensu Fungi)(p=-7.197754,f=1,n=3,id=GO:0030461) | GG;CATG | -11.3557 |
Mod 2040 | mating (sensu Fungi) | 0.8 | 4 | e--11 | 70 | 11 | mating (sensu Fungi)(p=-11.229733,f=0.8,n=4,id=GO:0030461) | ||
Mod 1966 | mating (sensu Fungi) | 0.692 | 9 | e--25 | 63 | 23 | mating (sensu Saccharomyces)(p=-21.50426,f=0.615,n=8,id=GO:0007322) | ATG4GTC | -12.3978 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 15 | main pathways of carbohydrate metabolism | 0.307 | 4 | e--8 | 81 | 24 | main pathways of carbohydrate metabolism(p=-8.230189,f=0.307,n=4,id=GO:0006092) | CGG;CCC | -11.7526 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 2780 | macromolecule catabolism | 0.159 | 43 | e--39 | 16 | 440 | proteolysis and peptidolysis(p=-43.379669,f=0.144,n=39,id=GO:0006508) | GTGGCAA | -18.8322 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1123 | mRNA splicing | 0.285 | 6 | e--11 | 17 | 32 | mRNA splicing(p=-11.087568,f=0.285,n=6,id=GO:0006371) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 2554 | mRNA metabolism | 0.285 | 4 | e--8 | 8 | 21 | mRNA metabolism(p=-8.199407,f=0.285,n=4,id=GO:0016071) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 2722 | lipid metabolism | 0.205 | 8 | e--8 | 13 | 61 | ER to Golgi transport(p=-6.546932,f=0.128,n=5,id=GO:0006888) | ||
Mod 2720 | lipid metabolism | 0.191 | 14 | e--16 | 24 | 112 | ergosterol metabolism(p=-13.600803,f=0.095,n=7,id=GO:0008204) | ||
Mod 2746 | lipid metabolism | 0.189 | 15 | e--17 | 21 | 98 | protein biosynthesis(p=-25.439884,f=0.316,n=25,id=GO:0006412) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1219 | lagging strand elongation | 0.384 | 5 | e--18 | 74 | 14 | lagging strand elongation(p=-18.158463,f=0.384,n=5,id=GO:0006273) | ACGCGT | -24.383 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 142 | iron-siderophore transport | 0.8 | 4 | e--21 | 228 | 8 | iron-siderophore transport(p=-21.759569,f=0.8,n=4,id=GO:0015892) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 831 | iron transport | 0.13 | 3 | e--7 | 16 | 51 | iron-siderophore transport(p=-14.572774,f=0.173,n=4,id=GO:0015892) | CCGCGG | -16.0445 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 2271 | ion transport | 1 | 3 | e--7 | 130 | 4 | ion transport(p=-7.531873,f=1,n=3,id=GO:0006811) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1569 | inorganic anion transport | 0.3 | 3 | e--8 | 100 | 12 | sulfate assimilation(p=-9.936847,f=0.3,n=3,id=GO:0000103) | CACGTG | -21.9822 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 2384 | histidine biosynthesis | 0.3 | 3 | e--8 | 106 | 12 | histidine biosynthesis(p=-8.643532,f=0.3,n=3,id=GO:0000105) | TGACTC | -12.8818 |
Mod 3069 | histidine biosynthesis | 0.133 | 4 | e--9 | 100 | 35 | amino acid metabolism(p=-51.03999,f=0.633,n=19,id=GO:0006520) | TGACTC | -45.2792 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 352 | hexose transport | 0.6 | 3 | e--9 | 92 | 6 | hexose transport(p=-9.631981,f=0.6,n=3,id=GO:0008645) | ||
Mod 3141 | hexose transport | 0.5 | 4 | e--13 | 38 | 12 | hexose transport(p=-13.123286,f=0.5,n=4,id=GO:0008645) | AGGCAC | -11.3265 |
Mod 3166 | hexose transport | 0.428 | 6 | e--20 | 8 | 31 | hexose transport(p=-20.693803,f=0.428,n=6,id=GO:0008645) | CGCGGA | -13.6235 |
Mod 2390 | hexose transport | 0.333 | 7 | e--22 | 55 | 32 | hexose transport(p=-22.961487,f=0.333,n=7,id=GO:0008645) | CC6CTCC | -14.6635 |
Mod 1028 | hexose transport | 0.222 | 8 | e--23 | 20 | 49 | hexose transport(p=-23.587561,f=0.222,n=8,id=GO:0008645) | TG1GGGG | -11.6202 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 3122 | hexose metabolism | 0.5 | 3 | e--7 | 54 | 8 | hexose metabolism(p=-7.054323,f=0.5,n=3,id=GO:0019318) | ||
Mod 1235 | hexose metabolism | 0.24 | 6 | e--12 | 37 | 37 | catabolic carbohydrate metabolism(p=-12.921055,f=0.24,n=6,id=GO:0006095) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1672 | heavy metal ion transport | 1 | 3 | e--9 | 224 | 3 | heavy metal ion transport(p=-9.88046,f=1,n=3,id=GO:0006823) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 719 | glycerophospholipid metabolism | 0.6 | 3 | e--10 | 80 | 6 | glycerophospholipid metabolism(p=-10.366097,f=0.6,n=3,id=GO:0006650) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 2978 | glutamine family amino acid metabolism | 0.444 | 4 | e--10 | 35 | 15 | glutamine family amino acid metabolism(p=-10.831896,f=0.444,n=4,id=GO:0009064) | GCT3CCG | -11.7869 |
Mod 1088 | glutamine family amino acid metabolism | 0.23 | 12 | e--31 | 26 | 72 | amino acid metabolism(p=-44.173355,f=0.403,n=21,id=GO:0006520) | GATAAG | -25.384 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1726 | glutamine family amino acid catabolism | 0.666 | 4 | e--17 | 118 | 7 | asparagine metabolism(p=-20.373615,f=0.666,n=4,id=GO:0006528) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1319 | glutamine family amino acid biosynthesis | 0.3 | 3 | e--7 | 135 | 15 | sulfate assimilation(p=-16.128527,f=0.4,n=4,id=GO:0000103) | ||
Mod 1088 | glutamine family amino acid biosynthesis | 0.153 | 8 | e--19 | 26 | 72 | amino acid metabolism(p=-44.173355,f=0.403,n=21,id=GO:0006520) | GATAAG | -25.384 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1630 | glutamate biosynthesis | 0.153 | 4 | e--10 | 6 | 64 | iron-siderophore transport(p=-14.153902,f=0.153,n=4,id=GO:0015892) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 853 | glucose transport | 0.107 | 3 | e--8 | 13 | 92 | glucose transport(p=-8.408349,f=0.107,n=3,id=GO:0015758) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 3093 | glucose metabolism | 0.727 | 8 | e--31 | 147 | 12 | glucose metabolism(p=-31.439676,f=0.727,n=8,id=GO:0006006) | ||
Mod 1234 | glucose metabolism | 0.163 | 9 | e--19 | 7 | 84 | gluconeogenesis(p=-30.177256,f=0.181,n=10,id=GO:0006094) | ||
Mod 1248 | glucose metabolism | 0.117 | 10 | e--19 | 56 | 143 | carbohydrate metabolism(p=-27.518203,f=0.235,n=20,id=GO:0005975) | AAGGGG | -31.308 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 3093 | gluconeogenesis | 0.636 | 7 | e--29 | 147 | 12 | glucose metabolism(p=-31.439676,f=0.727,n=8,id=GO:0006006) | ||
Mod 1234 | gluconeogenesis | 0.181 | 10 | e--30 | 7 | 84 | gluconeogenesis(p=-30.177256,f=0.181,n=10,id=GO:0006094) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 3270 | galactose metabolism | 0.666 | 6 | e--30 | 40 | 12 | galactose metabolism(p=-30.907865,f=0.666,n=6,id=GO:0006012) | CGG;CCG | -20.074 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 3093 | fermentation | 0.272 | 3 | e--8 | 147 | 12 | glucose metabolism(p=-31.439676,f=0.727,n=8,id=GO:0006006) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 2352 | fatty acid oxidation | 0.375 | 3 | e--10 | 28 | 15 | fatty acid oxidation(p=-10.223676,f=0.375,n=3,id=GO:0019395) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 3121 | fatty acid metabolism | 0.375 | 3 | e--7 | 70 | 10 | fatty acid metabolism(p=-7.28063,f=0.375,n=3,id=GO:0006631) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 3120 | fatty acid biosynthesis | 0.428 | 3 | e--10 | 78 | 9 | fatty acid biosynthesis(p=-10.96391,f=0.428,n=3,id=GO:0006633) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 2424 | fat-soluble vitamin metabolism | 1 | 3 | e--9 | 111 | 6 | vitamin B1 metabolism(p=-11.307577,f=1,n=3,id=GO:0006772) | ||
Mod 840 | fat-soluble vitamin metabolism | 0.21 | 4 | e--8 | 63 | 29 | hexose transport(p=-18.651663,f=0.315,n=6,id=GO:0008645) | AGGCAC | -13.4549 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 2919 | exocytosis | 0.357 | 5 | e--7 | 14 | 24 | exocytosis(p=-7.896659,f=0.357,n=5,id=GO:0006887) | ||
Mod 1092 | exocytosis | 0.23 | 6 | e--7 | 16 | 38 | exocytosis(p=-7.300206,f=0.23,n=6,id=GO:0006887) | ||
Mod 2703 | exocytosis | 0.228 | 8 | e--10 | 24 | 53 | exocytosis(p=-10.203844,f=0.228,n=8,id=GO:0006887) | ||
Mod 624 | exocytosis | 0.118 | 13 | e--10 | 1 | 220 | exocytosis(p=-10.203078,f=0.118,n=13,id=GO:0006887) | ||
Mod 3267 | exocytosis | 0.114 | 14 | e--10 | 0 | 190 | amino acid metabolism(p=-30.013188,f=0.188,n=23,id=GO:0006520) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 839 | establishment of cell polarity (sensu Fungi) | 0.125 | 6 | e--7 | 2 | 109 | response to abiotic stimulus(p=-11.392006,f=0.208,n=10,id=GO:0009628) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 2194 | ergosterol metabolism | 1 | 3 | e--10 | 92 | 3 | ergosterol metabolism(p=-10.130896,f=1,n=3,id=GO:0008204) | ||
Mod 1146 | ergosterol metabolism | 0.857 | 6 | e--26 | 62 | 10 | ergosterol metabolism(p=-26.574879,f=0.857,n=6,id=GO:0008204) | CCGATA | -13.3525 |
Mod 145 | ergosterol metabolism | 0.481 | 13 | e--52 | 24 | 35 | ergosterol metabolism(p=-52.109587,f=0.481,n=13,id=GO:0008204) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 2232 | energy derivation by oxidation of organic compounds | 0.8 | 4 | e--9 | 87 | 6 | energy derivation by oxidation of organic compounds(p=-9.9912,f=0.8,n=4,id=GO:0015980) | ||
Mod 323 | energy derivation by oxidation of organic compounds | 0.615 | 8 | e--18 | 56 | 14 | energy derivation by oxidation of organic compounds(p=-18.289047,f=0.615,n=8,id=GO:0015980) | ||
Mod 2229 | energy derivation by oxidation of organic compounds | 0.529 | 9 | e--18 | 54 | 24 | energy derivation by oxidation of organic compounds(p=-18.986128,f=0.529,n=9,id=GO:0015980) | ||
Mod 1103 | energy derivation by oxidation of organic compounds | 0.482 | 27 | e--60 | 83 | 76 | energy derivation by oxidation of organic compounds(p=-60.191008,f=0.482,n=27,id=GO:0015980) | CCAATC | -18.3177 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 895 | energy coupled proton transport\, down the electrochemical gradient | 0.2 | 5 | e--14 | 108 | 29 | phosphorylation(p=-15.696222,f=0.32,n=8,id=GO:0016310) | GGGGGC | -11.5413 |
Mod 1103 | energy coupled proton transport\, down the electrochemical gradient | 0.178 | 10 | e--35 | 83 | 76 | energy derivation by oxidation of organic compounds(p=-60.191008,f=0.482,n=27,id=GO:0015980) | CCAATC | -18.3177 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 326 | electron transport | 0.3 | 3 | e--7 | 83 | 12 | aerobic respiration(p=-13.847368,f=0.5,n=5,id=GO:0009060) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 832 | disaccharide metabolism | 0.187 | 3 | e--7 | 103 | 32 | disaccharide metabolism(p=-7.894492,f=0.187,n=3,id=GO:0005984) | TT8CCCC | -17.469 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1672 | di-\, tri-valent inorganic cation transport | 1 | 3 | e--9 | 224 | 3 | heavy metal ion transport(p=-9.88046,f=1,n=3,id=GO:0006823) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1169 | degradation of cyclin | 0.1 | 5 | e--11 | 10 | 77 | spore wall assembly (sensu Saccharomyces)(p=-16.921709,f=0.14,n=7,id=GO:0007152) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 2485 | cytoskeleton organization and biogenesis | 0.163 | 15 | e--10 | 13 | 154 | cytoskeleton organization and biogenesis(p=-10.451994,f=0.163,n=15,id=GO:0007010) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1328 | cytokinesis | 0.6 | 3 | e--8 | 151 | 6 | cytokinesis(p=-8.277505,f=0.6,n=3,id=GO:0016288) | ||
Mod 1714 | cytokinesis | 0.454 | 5 | e--14 | 52 | 17 | cytokinesis(p=-14.032932,f=0.454,n=5,id=GO:0016288) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 831 | copper ion transport | 0.173 | 4 | e--11 | 16 | 51 | iron-siderophore transport(p=-14.572774,f=0.173,n=4,id=GO:0015892) | CCGCGG | -16.0445 |
Mod 914 | copper ion transport | 0.121 | 5 | e--14 | 10 | 71 | copper ion transport(p=-14.032932,f=0.121,n=5,id=GO:0006825) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 3103 | complex III (ubiquinone to cytochrome c) | 0.333 | 5 | e--20 | 112 | 18 | aerobic respiration(p=-30.056224,f=0.6,n=9,id=GO:0009060) | ||
Mod 1103 | complex III (ubiquinone to cytochrome c) | 0.125 | 7 | e--24 | 83 | 76 | energy derivation by oxidation of organic compounds(p=-60.191008,f=0.482,n=27,id=GO:0015980) | CCAATC | -18.3177 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 652 | coenzymes and prosthetic group metabolism | 0.323 | 11 | e--22 | 23 | 69 | pyridoxine metabolism(p=-25.391885,f=0.176,n=6,id=GO:0008614) | AGGCAC | -13.5304 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 2503 | coenzyme metabolism | 0.6 | 3 | e--7 | 16 | 10 | coenzyme metabolism(p=-7.587826,f=0.6,n=3,id=GO:0006732) | ||
Mod 1317 | coenzyme metabolism | 0.5 | 4 | e--10 | 18 | 20 | coenzyme metabolism(p=-10.011205,f=0.5,n=4,id=GO:0006732) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1488 | coenzyme biosynthesis | 1 | 4 | e--16 | 45 | 8 | nicotinamide adenine dinucleotide metabolism(p=-18.813318,f=1,n=4,id=GO:0019674) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1512 | chromosome condensation | 0.25 | 3 | e--7 | 13 | 23 | mitotic prophase(p=-7.050448,f=0.25,n=3,id=GO:0000088) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1470 | chromatin assembly/disassembly | 1 | 6 | e--28 | 79 | 15 | chromatin assembly/disassembly(p=-28.243643,f=1,n=6,id=GO:0006333) | GCG:AAC | -15.27 |
Mod 2610 | chromatin assembly/disassembly | 0.888 | 8 | e--39 | 200 | 10 | chromatin assembly/disassembly(p=-39.451674,f=0.888,n=8,id=GO:0006333) | GT9TTCG | -19.1456 |
Mod 969 | chromatin assembly/disassembly | 0.142 | 9 | e--23 | 58 | 92 | DNA metabolism(p=-58.77429,f=0.539,n=34,id=GO:0006259) | ACGCGT | -78.5011 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1975 | cell-cell fusion | 0.508 | 30 | e--84 | 51 | 93 | mating (sensu Saccharomyces)(p=-79.978314,f=0.491,n=29,id=GO:0007322) | TGAAAC | -25.2808 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 3182 | cell wall organization and biogenesis | 0.6 | 6 | e--14 | 108 | 18 | cell wall organization and biogenesis(p=-14.197326,f=0.6,n=6,id=GO:0007047) | TTCGCG | -12.4048 |
Mod 839 | cell wall organization and biogenesis | 0.187 | 9 | e--10 | 2 | 109 | response to abiotic stimulus(p=-11.392006,f=0.208,n=10,id=GO:0009628) | ||
Mod 818 | cell wall organization and biogenesis | 0.144 | 10 | e--10 | 4 | 155 | cell wall organization and biogenesis(p=-10.134928,f=0.144,n=10,id=GO:0007047) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 3061 | cell surface receptor linked signal transduction | 0.2 | 4 | e--7 | 4 | 44 | cell surface receptor linked signal transduction(p=-7.422033,f=0.2,n=4,id=GO:0007166) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 619 | cell cycle control | 0.333 | 6 | e--11 | 69 | 29 | mitotic cell cycle(p=-24.681719,f=0.666,n=12,id=GO:0000278) | AACGCG | -13.6558 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 2030 | cell cycle checkpoint | 0.25 | 4 | e--9 | 60 | 21 | cell cycle checkpoint(p=-9.318548,f=0.25,n=4,id=GO:0000075) | ACGCGA | -18.8069 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 2711 | cation transport | 0.101 | 8 | e--9 | 20 | 105 | cation transport(p=-9.564482,f=0.101,n=8,id=GO:0006812) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 3093 | catabolism | 0.727 | 8 | e--16 | 147 | 12 | glucose metabolism(p=-31.439676,f=0.727,n=8,id=GO:0006006) | ||
Mod 2795 | catabolism | 0.45 | 27 | e--44 | 53 | 87 | ubiquitin-dependent protein degradation(p=-48.183607,f=0.366,n=22,id=GO:0006511) | GGTGGC | -20.1839 |
Mod 982 | catabolism | 0.359 | 41 | e--58 | 64 | 184 | ubiquitin-dependent protein degradation(p=-60.023724,f=0.271,n=31,id=GO:0006511) | AAGGGG | -20.3047 |
Mod 2780 | catabolism | 0.178 | 48 | e--36 | 16 | 440 | proteolysis and peptidolysis(p=-43.379669,f=0.144,n=39,id=GO:0006508) | GTGGCAA | -18.8322 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 3093 | catabolic carbohydrate metabolism | 0.727 | 8 | e--29 | 147 | 12 | glucose metabolism(p=-31.439676,f=0.727,n=8,id=GO:0006006) | ||
Mod 1234 | catabolic carbohydrate metabolism | 0.163 | 9 | e--17 | 7 | 84 | gluconeogenesis(p=-30.177256,f=0.181,n=10,id=GO:0006094) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 2994 | carbohydrate transport | 0.666 | 4 | e--13 | 47 | 10 | carbohydrate transport(p=-13.673722,f=0.666,n=4,id=GO:0008643) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1629 | carbohydrate metabolism | 0.5 | 9 | e--18 | 147 | 29 | carbohydrate metabolism(p=-18.425717,f=0.5,n=9,id=GO:0005975) | AGG9GGG | -16.898 |
Mod 1087 | carbohydrate metabolism | 0.252 | 23 | e--33 | 157 | 186 | stress response(p=-34.175841,f=0.263,n=24,id=GO:0006950) | AAGGGG | -64.6463 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 3125 | branched chain family amino acid biosynthesis | 0.333 | 5 | e--18 | 75 | 19 | branched chain family amino acid biosynthesis(p=-18.751502,f=0.333,n=5,id=GO:0009082) | TGA1TCA | -12.1388 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1371 | axial budding | 0.25 | 3 | e--7 | 69 | 16 | axial budding(p=-7.276382,f=0.25,n=3,id=GO:0007120) | TT9CGCG | -12.9431 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 3105 | autophagy | 0.25 | 7 | e--20 | 0 | 52 | autophagy(p=-20.508202,f=0.25,n=7,id=GO:0006914) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 3133 | aspartate family amino acid metabolism | 0.47 | 8 | e--26 | 100 | 26 | sulfate assimilation(p=-35.182758,f=0.411,n=7,id=GO:0000103) | CACGTG | -20.1247 |
Mod 1088 | aspartate family amino acid metabolism | 0.173 | 9 | e--20 | 26 | 72 | amino acid metabolism(p=-44.173355,f=0.403,n=21,id=GO:0006520) | GATAAG | -25.384 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1726 | asparagine metabolism | 0.666 | 4 | e--20 | 118 | 7 | asparagine metabolism(p=-20.373615,f=0.666,n=4,id=GO:0006528) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 3095 | aromatic amino acid family biosynthesis | 0.6 | 3 | e--10 | 133 | 5 | aromatic amino acid family biosynthesis(p=-10.519907,f=0.6,n=3,id=GO:0009073) | ||
Mod 945 | aromatic amino acid family biosynthesis | 0.266 | 8 | e--28 | 75 | 46 | amino acid metabolism(p=-81.082855,f=0.833,n=25,id=GO:0006520) | TGACTC | -22.1457 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1002 | arginine metabolism | 0.3 | 3 | e--8 | 9 | 26 | arginine metabolism(p=-8.296545,f=0.3,n=3,id=GO:0006525) | TTA5AGG | -12.6865 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 3057 | arginine biosynthesis | 0.6 | 9 | e--49 | 148 | 16 | amino acid biosynthesis(p=-48.053881,f=0.866,n=13,id=GO:0008652) | TGACTC | -39.5394 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 3079 | amino acid transport | 1 | 4 | e--16 | 98 | 4 | amino acid transport(p=-16.0512,f=1,n=4,id=GO:0006865) | ||
Mod 3224 | amino acid transport | 0.7 | 7 | e--29 | 32 | 13 | amino acid transport(p=-29.473613,f=0.7,n=7,id=GO:0006865) | TTGCCG | -11.5499 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 945 | amino acid metabolism | 0.833 | 25 | e--81 | 75 | 46 | amino acid metabolism(p=-81.082855,f=0.833,n=25,id=GO:0006520) | TGACTC | -22.1457 |
Mod 848 | amino acid metabolism | 0.569 | 41 | e--111 | 93 | 112 | amino acid metabolism(p=-111.10627,f=0.569,n=41,id=GO:0006520) | TGACTC | -57.0046 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 3057 | amino acid biosynthesis | 0.866 | 13 | e--48 | 148 | 16 | amino acid biosynthesis(p=-48.053881,f=0.866,n=13,id=GO:0008652) | TGACTC | -39.5394 |
Mod 945 | amino acid biosynthesis | 0.666 | 20 | e--66 | 75 | 46 | amino acid metabolism(p=-81.082855,f=0.833,n=25,id=GO:0006520) | TGACTC | -22.1457 |
Mod 848 | amino acid biosynthesis | 0.472 | 34 | e--102 | 93 | 112 | amino acid metabolism(p=-111.10627,f=0.569,n=41,id=GO:0006520) | TGACTC | -57.0046 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1093 | amino acid and derivative metabolism | 0.647 | 11 | e--27 | 58 | 25 | tryptophan biosynthesis(p=-13.480959,f=0.235,n=4,id=GO:0000162) | TGACTCA | -13.9284 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 2605 | amino acid activation | 0.129 | 4 | e--7 | 54 | 41 | amino acid activation(p=-7.98621,f=0.129,n=4,id=GO:0006418) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 654 | aldehyde metabolism | 0.7 | 7 | e--37 | 62 | 15 | aldehyde metabolism(p=-37.036371,f=0.7,n=7,id=GO:0006081) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 3103 | aerobic respiration | 0.6 | 9 | e--30 | 112 | 18 | aerobic respiration(p=-30.056224,f=0.6,n=9,id=GO:0009060) | ||
Mod 1103 | aerobic respiration | 0.285 | 16 | e--42 | 83 | 76 | energy derivation by oxidation of organic compounds(p=-60.191008,f=0.482,n=27,id=GO:0015980) | CCAATC | -18.3177 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 2077 | TCA intermediate metabolism | 0.275 | 8 | e--25 | 63 | 45 | tricarboxylic acid cycle(p=-29.157554,f=0.275,n=8,id=GO:0006099) | CGG7CAA | -12.1457 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 3045 | S phase of mitotic cell cycle | 0.571 | 4 | e--9 | 54 | 17 | S phase of mitotic cell cycle(p=-9.529401,f=0.571,n=4,id=GO:0000084) | ACGCGT | -14.2526 |
Mod 969 | S phase of mitotic cell cycle | 0.285 | 18 | e--38 | 58 | 92 | DNA metabolism(p=-58.77429,f=0.539,n=34,id=GO:0006259) | ACGCGT | -78.5011 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 3040 | RNA processing | 0.666 | 6 | e--12 | 154 | 19 | transcription\, from Pol I promoter(p=-16.510518,f=0.666,n=6,id=GO:0006360) | AAAATTT | -14.2696 |
Mod 1004 | RNA processing | 0.562 | 9 | e--17 | 175 | 30 | transcription\, from Pol I promoter(p=-19.677218,f=0.5,n=8,id=GO:0006360) | GATGAG | -23.7476 |
Mod 2663 | RNA processing | 0.545 | 12 | e--23 | 183 | 47 | RNA processing(p=-23.033189,f=0.545,n=12,id=GO:0006396) | GATGAG | -26.1875 |
Mod 911 | RNA processing | 0.46 | 41 | e--78 | 180 | 185 | ribosome biogenesis(p=-144.589732,f=0.561,n=50,id=GO:0007046) | GATGAG | -84.8431 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 2679 | RNA modification | 0.21 | 4 | e--8 | 136 | 39 | transcription\, from Pol I promoter(p=-14.336101,f=0.368,n=7,id=GO:0006360) | CGA3GAT | -13.6631 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 2768 | N-linked glycosylation | 0.153 | 4 | e--7 | 18 | 37 | N-linked glycosylation(p=-7.13638,f=0.153,n=4,id=GO:0006487) | ||
Mod 1040 | N-linked glycosylation | 0.111 | 5 | e--8 | 17 | 78 | N-linked glycosylation(p=-8.135072,f=0.111,n=5,id=GO:0006487) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 2974 | M-phase specific microtubule process | 0.13 | 20 | e--39 | 13 | 247 | nuclear division(p=-83.02673,f=0.333,n=51,id=GO:0000280) | CACAAA | -47.4602 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 2974 | M phase | 0.359 | 55 | e--81 | 13 | 247 | nuclear division(p=-83.02673,f=0.333,n=51,id=GO:0000280) | CACAAA | -47.4602 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 2958 | G2/M transition of mitotic cell cycle | 0.333 | 3 | e--7 | 16 | 12 | G2/M transition of mitotic cell cycle(p=-7.019372,f=0.333,n=3,id=GO:0000086) | ATT9TTG | -11.3863 |
Mod 619 | G2/M transition of mitotic cell cycle | 0.277 | 5 | e--12 | 69 | 29 | mitotic cell cycle(p=-24.681719,f=0.666,n=12,id=GO:0000278) | AACGCG | -13.6558 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 619 | G1/S transition of mitotic cell cycle | 0.277 | 5 | e--12 | 69 | 29 | mitotic cell cycle(p=-24.681719,f=0.666,n=12,id=GO:0000278) | AACGCG | -13.6558 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 887 | ER to Golgi transport | 0.6 | 3 | e--7 | 33 | 9 | ER to Golgi transport(p=-7.551802,f=0.6,n=3,id=GO:0006888) | ||
Mod 2719 | ER to Golgi transport | 0.357 | 5 | e--11 | 20 | 25 | ER to Golgi transport(p=-11.213016,f=0.357,n=5,id=GO:0006888) | CGA7ACT | -12.6877 |
Mod 2748 | ER to Golgi transport | 0.105 | 9 | e--11 | 11 | 133 | mitochondrial translocation(p=-10.121179,f=0.07,n=6,id=GO:0006628) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1067 | DNA unwinding | 0.138 | 5 | e--14 | 39 | 50 | pre-replicative complex formation and maintenance(p=-14.600786,f=0.138,n=5,id=GO:0006267) | CC6GGAA | -16.6593 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 969 | DNA strand elongation | 0.158 | 10 | e--25 | 58 | 92 | DNA metabolism(p=-58.77429,f=0.539,n=34,id=GO:0006259) | ACGCGT | -78.5011 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 1067 | DNA replication initiation | 0.138 | 5 | e--11 | 39 | 50 | pre-replicative complex formation and maintenance(p=-14.600786,f=0.138,n=5,id=GO:0006267) | CC6GGAA | -16.6593 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 3161 | DNA replication and chromosome cycle | 0.666 | 4 | e--8 | 78 | 7 | DNA replication and chromosome cycle(p=-8.083417,f=0.666,n=4,id=GO:0000067) | ||
Mod 1390 | DNA replication and chromosome cycle | 0.545 | 6 | e--11 | 64 | 18 | DNA strand elongation(p=-6.798618,f=0.272,n=3,id=GO:0006271) | ACGCGT | -22.9339 |
Mod 619 | DNA replication and chromosome cycle | 0.5 | 9 | e--16 | 69 | 29 | mitotic cell cycle(p=-24.681719,f=0.666,n=12,id=GO:0000278) | AACGCG | -13.6558 |
Mod 969 | DNA replication and chromosome cycle | 0.38 | 24 | e--41 | 58 | 92 | DNA metabolism(p=-58.77429,f=0.539,n=34,id=GO:0006259) | ACGCGT | -78.5011 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 969 | DNA repair | 0.222 | 14 | e--23 | 58 | 92 | DNA metabolism(p=-58.77429,f=0.539,n=34,id=GO:0006259) | ACGCGT | -78.5011 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 3045 | DNA metabolism | 0.714 | 5 | e--9 | 54 | 17 | S phase of mitotic cell cycle(p=-9.529401,f=0.571,n=4,id=GO:0000084) | ACGCGT | -14.2526 |
Mod 969 | DNA metabolism | 0.539 | 34 | e--58 | 58 | 92 | DNA metabolism(p=-58.77429,f=0.539,n=34,id=GO:0006259) | ACGCGT | -78.5011 |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 3084 | DNA dependent DNA replication | 0.6 | 3 | e--7 | 133 | 6 | DNA dependent DNA replication(p=-7.447537,f=0.6,n=3,id=GO:0006261) |
Module | Enirched GO Entry | Class Fraction | Class Genes | Class p-value | Mod #conditions | Mod #genes | Most Enriched | Motif | Motif p-value |
Mod 2644 | 35S primary transcript processing | 0.428 | 3 | e--7 | 196 | 12 | 35S primary transcript processing(p=-7.191856,f=0.428,n=3,id=GO:0006365) | AA2TCAT | -11.6806 |
Mod 249 | 35S primary transcript processing | 0.363 | 4 | e--9 | 189 | 17 | 35S primary transcript processing(p=-9.798536,f=0.363,n=4,id=GO:0006365) | AAATTT | -11.4892 |
Mod 1808 | 35S primary transcript processing | 0.357 | 5 | e--12 | 187 | 30 | transcription\, from Pol I promoter(p=-36.086249,f=0.785,n=11,id=GO:0006360) | GATGAG | -16.4503 |
Mod 2663 | 35S primary transcript processing | 0.318 | 7 | e--18 | 183 | 47 | RNA processing(p=-23.033189,f=0.545,n=12,id=GO:0006396) | GATGAG | -26.1875 |
Mod 911 | 35S primary transcript processing | 0.258 | 23 | e--69 | 180 | 185 | ribosome biogenesis(p=-144.589732,f=0.561,n=50,id=GO:0007046) | GATGAG | -84.8431 |