| Std2 GX | %ile | GSM ID | Assay name | GSE ID | Experiment title | Link to GEO |
| 341.1 | 100.0 | ArrayExpress | E-MEXP-1474-raw-cel-1593932865 | - | - | - |
| 298.6 | 100.0 | ArrayExpress | E-MEXP-1474-raw-cel-1593932801 | - | - | - |
| 216.9 | 100.0 | ArrayExpress | E-MEXP-1474-raw-cel-1593932929 | - | - | - |
| 215.7 | 100.0 | GSM184551 | Whole roots 2hr KCl control treated then incubated in protoplast-generating solution minus enzymes, biological rep1 | GSE7631 | Cell-specific nitrogen responses in the Arabidopsis root |  |
| 136.5 | 99.9 | ArrayExpress | E-NASC-76-raw-cel-1359879158 | - | - | - |
| 119.9 | 99.9 | ArrayExpress | E-MEXP-1474-raw-cel-1593932897 | - | - | - |
| 117.2 | 99.9 | GSM270866 | Arabidopsis cell culture, 4 h_response to phytoprostane A1_rep1 | GSE10719 | Response of Arabidopsis cell culture to phytoprostane A1 | |
| 111.0 | 99.9 | GSM184497 | Endodermis&Pericycle root cells 2hr transitory KNO3 treated, biological rep1 | GSE7631 | Cell-specific nitrogen responses in the Arabidopsis root | |
| 110.8 | 99.9 | GSM270868 | Arabidopsis cell culture, 4 h_response to phytoprostane A1_rep2 | GSE10719 | Response of Arabidopsis cell culture to phytoprostane A1 | |
| 105.7 | 99.9 | GSM270814 | Arabidopsis cell culture, 4 h_control_rep1 | GSE10719 | Response of Arabidopsis cell culture to phytoprostane A1 | |
| 99.5 | 99.9 | GSM270870 | Arabidopsis cell culture, 4 h_response to phytoprostane A1_rep3 | GSE10719 | Response of Arabidopsis cell culture to phytoprostane A1 | |
| 94.7 | 99.9 | GSM143300 | Ts_genomic_hyb_3 | GSE6203 | Rus_etal_High_Na_Arabidopsis_accessions_mapping_HKT1 | |
| 73.8 | 99.9 | GSM143298 | Low_Na_seg_pool_ts_col_F2 | GSE6203 | Rus_etal_High_Na_Arabidopsis_accessions_mapping_HKT1 | |
| 70.0 | 99.9 | GSM143306 | High_Na_seg_pool_tsu_col_F2 | GSE6203 | Rus_etal_High_Na_Arabidopsis_accessions_mapping_HKT1 | |
| 69.1 | 99.9 | GSM143301 | Ts_genomic_hyb_2 | GSE6203 | Rus_etal_High_Na_Arabidopsis_accessions_mapping_HKT1 | |
| 61.9 | 99.8 | ArrayExpress | E-NASC-76-raw-cel-1359878976 | - | - | - |
| 61.7 | 99.8 | GSM253651 | Ler 1 | GSE10039 | Low_Mo_Arabidopsis_mapping_MOT1 | |
| 61.0 | 99.8 | GSM143310 | Tsu_genomic_hyb_1 | GSE6203 | Rus_etal_High_Na_Arabidopsis_accessions_mapping_HKT1 | |
| 57.8 | 99.8 | GSM143299 | High_Na_seg_pool_ts_col_F2 | GSE6203 | Rus_etal_High_Na_Arabidopsis_accessions_mapping_HKT1 | |
| 57.5 | 99.8 | GSM143302 | Ts_genomic_hyb_1 | GSE6203 | Rus_etal_High_Na_Arabidopsis_accessions_mapping_HKT1 | |
| 57.4 | 99.8 | GSM143307 | Low_Na_seg_pool_tsu_col_F2 | GSE6203 | Rus_etal_High_Na_Arabidopsis_accessions_mapping_HKT1 | |
| 53.4 | 99.8 | GSM253645 | High_Mo_seg_pool_Ler_col_F2 | GSE10039 | Low_Mo_Arabidopsis_mapping_MOT1 | |
| 52.8 | 99.8 | GSM184552 | Whole roots 2hr KCl control treated then incubated in protoplast-generating solution minus enzymes, biological rep2 | GSE7631 | Cell-specific nitrogen responses in the Arabidopsis root | |
| 52.5 | 99.8 | GSM253646 | Low_Mo_seg_pool_Ler_col_F2 | GSE10039 | Low_Mo_Arabidopsis_mapping_MOT1 | |
| 51.4 | 99.8 | GSM253649 | Col-0-2 | GSE10039 | Low_Mo_Arabidopsis_mapping_MOT1 | |
| 51.2 | 99.8 | GSM143309 | Tsu_genomic_hyb_2 | GSE6203 | Rus_etal_High_Na_Arabidopsis_accessions_mapping_HKT1 | |
| 50.0 | 99.8 | GSM253648 | Col-0-1 | GSE10039 | Low_Mo_Arabidopsis_mapping_MOT1 | |
| 49.7 | 99.8 | GSM143308 | Tsu_genomic_hyb_3 | GSE6203 | Rus_etal_High_Na_Arabidopsis_accessions_mapping_HKT1 | |
| 49.2 | 99.8 | GSM253652 | Ler 2 | GSE10039 | Low_Mo_Arabidopsis_mapping_MOT1 | |
| 47.4 | 99.8 | ArrayExpress | E-MEXP-1474-raw-cel-1593932833 | - | - | - |
| 46.8 | 99.8 | GSM270853 | Arabidopsis cell culture, 4 h_control_rep2 | GSE10719 | Response of Arabidopsis cell culture to phytoprostane A1 | |
| 45.0 | 99.8 | GSM253647 | Col-0 3 | GSE10039 | Low_Mo_Arabidopsis_mapping_MOT1 | |
| 44.8 | 99.8 | GSM253650 | Ler 3 | GSE10039 | Low_Mo_Arabidopsis_mapping_MOT1 | |
| 39.2 | 99.8 | GSM204026 | protoplast_control_rep1 | GSE8248 | Identification of hypoxia-inducible genes in Arabidopsis mesophyll cells | |
| 38.6 | 99.8 | ArrayExpress | E-MEXP-1474-raw-cel-1593932769 | - | - | - |
| 36.1 | 99.7 | ArrayExpress | E-NASC-76-raw-cel-1359878900 | - | - | - |
| 36.0 | 99.7 | GSM142629 | MC002_ATH1_A3.1-dubos-6kx | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | |
| 28.0 | 99.7 | GSM142631 | MC002_ATH1_A3.3-dubos-6kx | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | |
| 25.3 | 99.6 | GSM142630 | MC002_ATH1_A3.2-dubos-6kx | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | |
| 25.1 | 99.6 | GSM270865 | Arabidopsis cell culture, 4 h_control_rep3 | GSE10719 | Response of Arabidopsis cell culture to phytoprostane A1 | |
| 24.9 | 99.6 | GSM142637 | MC002_ATH1_A5.3-dubos-5kx | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | |
| 21.6 | 99.6 | GSM142624 | MC002_ATH1_A1.2-dubos-wtx | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | |
| 21.5 | 99.6 | GSM142829 | GM001_ATH1_A11-Torres-5N3 | GSE6176 | Impact of Type III effectors on plant defense responses | |
| 21.0 | 99.6 | GSM142623 | MC002_ATH1_A1.1-dubos-wtx | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | |
| 20.9 | 99.6 | GSM131141 | AtGen_B-27_2-6-4_REP2_ATH1 | GSE5615 | AtGenExpress: Response to bacterial-(LPS, HrpZ, Flg22) and oomycete-(NPP1) derived elicitors | |
| 19.3 | 99.6 | GSM142636 | MC002_ATH1_A5.2-dubos-5kx | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | |
| 19.3 | 99.6 | GSM142830 | GM001_ATH1_A14-Torres-4N3_repeat2 | GSE6176 | Impact of Type III effectors on plant defense responses | |
| 17.7 | 99.5 | GSM131113 | AtGen_B-41_3-6-4_REP3_ATH1 | GSE5615 | AtGenExpress: Response to bacterial-(LPS, HrpZ, Flg22) and oomycete-(NPP1) derived elicitors | |
| 16.8 | 99.5 | ArrayExpress | E-MEXP-1474-raw-cel-1593932737 | - | - | - |
| 15.4 | 99.5 | ArrayExpress | E-MEXP-475-raw-cel-680982449 | - | - | - |
| 14.5 | 99.4 | ArrayExpress | E-ATMX-30-raw-cel-1513696830 | - | - | - |
| 13.0 | 99.4 | GSM128674 | Underwood_1-26_hrpA-10e8-7h_Rep2_ATH1 | GSE5520 | Genome-wide transcriptional analysis of the compatible A. thaliana-P. syringae pv. tomato DC3000 interaction | |
| 12.9 | 99.3 | GSM205435 | Col_ leaf_ wildtype_rep02 | GSE8279 | Transgenerational Stability of the Arabidopsis Epigenome Is Coordinated by CG Methylation | |
| 12.6 | 99.3 | GSM74908 | ice1_24H Cold_Rep1 | GSE3326 | ICE1 regulation of the Arabidopsis Cold-Responsive Transcriptome | |
| 12.2 | 99.3 | GSM131299 | AtGen_6-2511_Osmoticstress-Shoots-12.0h_Rep1 | GSE5622 | AtGenExpress: Stress Treatments (Osmotic stress) | |
| 11.3 | 99.3 | GSM133731 | Buchanan-Wollaston_A-3-bwoll-C0S_SLD | GSE5727 | The effects of mutants in stress response pathways on gene expression during senescence | |
| 10.9 | 99.2 | GSM142839 | MG001_ATH1_A18-Torres-6N6 | GSE6176 | Impact of Type III effectors on plant defense responses | |
| 10.8 | 99.2 | GSM131112 | AtGen_B-40_3-5-4_REP3_ATH1 | GSE5615 | AtGenExpress: Response to bacterial-(LPS, HrpZ, Flg22) and oomycete-(NPP1) derived elicitors | |
| 10.6 | 99.2 | ArrayExpress | E-MEXP-1474-raw-cel-1593932545 | - | - | - |
| 10.2 | 99.2 | GSM142635 | MC002_ATH1_A5.1-dubos-5kx | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | |
| 10.1 | 99.2 | GSM67086 | Arabidopsis_Stigma02 | GSE3056 | Arabidopsis Pollination Study | |
| 9.9 | 99.1 | GSM131140 | AtGen_B-26_2-5-4_REP2_ATH1 | GSE5615 | AtGenExpress: Response to bacterial-(LPS, HrpZ, Flg22) and oomycete-(NPP1) derived elicitors | |
| 9.9 | 99.1 | GSM131111 | AtGen_B-39_3-4-4_REP3_ATH1 | GSE5615 | AtGenExpress: Response to bacterial-(LPS, HrpZ, Flg22) and oomycete-(NPP1) derived elicitors | |
| 9.7 | 99.1 | ArrayExpress | E-NASC-76-raw-cel-1359879106 | - | - | - |
| 9.6 | 99.1 | GSM142835 | MG001_ATH1_A13-Torres-4N1 | GSE6176 | Impact of Type III effectors on plant defense responses | |
| 9.5 | 99.1 | GSM131127 | AtGen_B-13_1-6-4_REP1_ATH1 | GSE5615 | AtGenExpress: Response to bacterial-(LPS, HrpZ, Flg22) and oomycete-(NPP1) derived elicitors | |
| 9.3 | 99.1 | ArrayExpress | E-MEXP-1474-raw-cel-1593932641 | - | - | - |
| 9.3 | 99.1 | GSM133734 | Buchanan-Wollaston_A-6-bwoll-NG2_SLD | GSE5727 | The effects of mutants in stress response pathways on gene expression during senescence | |
| 9.2 | 99.1 | GSM128672 | Underwood_1-27_hrpA-10e8-7h_Rep3_ATH1 | GSE5520 | Genome-wide transcriptional analysis of the compatible A. thaliana-P. syringae pv. tomato DC3000 interaction | |
| 9.0 | 99.1 | GSM67087 | Arabidopsis_Stigma03 | GSE3056 | Arabidopsis Pollination Study | |
| 8.7 | 99.0 | GSM133733 | Buchanan-Wollaston_A-5-bwoll-NG1_SLD | GSE5727 | The effects of mutants in stress response pathways on gene expression during senescence | |
| 8.6 | 99.0 | GSM142836 | MG001_ATH1_A15-Torres-4N6 | GSE6176 | Impact of Type III effectors on plant defense responses | |
