Search results for the GEO ID: GSE43032  |
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|
GSM ID | GPL ID |
Select for analysis |
Title |
Source name |
Description |
Characteristics |
GSM1055335 | GPL570 |
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H295R/TR SF-1 cells, cultured in basal conditions for 72 hours
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H295R/TR SF-1 cell line
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cell line: H295R/TR
treatment: control
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Gene expression data from H295R/TR SF-1 cells cultured in basal conditions for 72 hours
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| Sample_geo_accession | GSM1055335
| | Sample_status | Public on Aug 01 2013
| | Sample_submission_date | Dec 19 2012
| | Sample_last_update_date | Aug 03 2013
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_treatment_protocol_ch1 | Sample H295R/TR SF-1 Dox was treated with doxycycline (Dox; 1 ug/mL)
| | Sample_growth_protocol_ch1 | H295R/TR SF-1 cells were grown in DMEM/F12 (Invitrogen) containing antibiotics, 2% NuSerum (BD Biosciences) an 1% ITS+ culture supplement (BD Biosciences) in 6-well plates
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | RNeasy Mini kit (Qiagen) following the manufacturer's procedures
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the GeneChip 3' IVT Express Affymetrix protocol from 2 ug total RNA
| | Sample_hyb_protocol | Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on HG-U133 Plus 2.0 arrays. Arrays were washed and stained in the Affymetrix Fluidics Station 400.
| | Sample_scan_protocol | GeneChips were scanned using the Hewlett-Packard GeneArray Scanner G2500A
| | Sample_data_processing | The data were analyzed with GC-RMA
| | Sample_platform_id | GPL570
| | Sample_contact_name | Enzo,,LALLI
| | Sample_contact_email | ninino@ipmc.cnrs.fr
| | Sample_contact_phone | +33 (0)4 93 95 77 55
| | Sample_contact_laboratory | 402
| | Sample_contact_department | CNRS UMR 7275
| | Sample_contact_institute | IPMC
| | Sample_contact_address | 660 route des Lucioles
| | Sample_contact_city | Valbonne
| | Sample_contact_zip/postal_code | 06560
| | Sample_contact_country | France
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM1055nnn/GSM1055335/suppl/GSM1055335_A680_01_CL_2.CEL.gz
| | Sample_series_id | GSE43032
| | Sample_series_id | GSE43035
| | Sample_data_row_count | 54613
| | |
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GSM1055336 | GPL570 |
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H295R/TR SF-1 cells, treated with doxycycline (1 ug/mL) for 72 hours
|
H295R/TR SF-1 cell line
|
cell line: H295R/TR
treatment: SF-1 overexpression
|
Gene expression data from H295R/TR SF-1 cells treated with doxycycline for 72 hours
|
| Sample_geo_accession | GSM1055336
| | Sample_status | Public on Aug 01 2013
| | Sample_submission_date | Dec 19 2012
| | Sample_last_update_date | Aug 03 2013
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_treatment_protocol_ch1 | Sample H295R/TR SF-1 Dox was treated with doxycycline (Dox; 1 ug/mL)
| | Sample_growth_protocol_ch1 | H295R/TR SF-1 cells were grown in DMEM/F12 (Invitrogen) containing antibiotics, 2% NuSerum (BD Biosciences) an 1% ITS+ culture supplement (BD Biosciences) in 6-well plates
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | RNeasy Mini kit (Qiagen) following the manufacturer's procedures
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the GeneChip 3' IVT Express Affymetrix protocol from 2 ug total RNA
| | Sample_hyb_protocol | Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on HG-U133 Plus 2.0 arrays. Arrays were washed and stained in the Affymetrix Fluidics Station 400.
| | Sample_scan_protocol | GeneChips were scanned using the Hewlett-Packard GeneArray Scanner G2500A
| | Sample_data_processing | The data were analyzed with GC-RMA
| | Sample_platform_id | GPL570
| | Sample_contact_name | Enzo,,LALLI
| | Sample_contact_email | ninino@ipmc.cnrs.fr
| | Sample_contact_phone | +33 (0)4 93 95 77 55
| | Sample_contact_laboratory | 402
| | Sample_contact_department | CNRS UMR 7275
| | Sample_contact_institute | IPMC
| | Sample_contact_address | 660 route des Lucioles
| | Sample_contact_city | Valbonne
| | Sample_contact_zip/postal_code | 06560
| | Sample_contact_country | France
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM1055nnn/GSM1055336/suppl/GSM1055336_A680_02_CL_2_DOX.CEL.gz
| | Sample_series_id | GSE43032
| | Sample_series_id | GSE43035
| | Sample_data_row_count | 54613
| | |
|
GSM1192155 | GPL570 |
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C_NT_01
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H295R/TR SF-1 cells, cultured in basal conditions for 72 hours
|
tissue: adrenal cortex
cell line: H295R/TR SF-1 cell line
treatment: cultured in basal conditions for 72 hours
|
Gene expression data from H295R/TR SF-1 cells cultured in basal conditions for 72 hours
|
| Sample_geo_accession | GSM1192155
| | Sample_status | Public on Aug 01 2013
| | Sample_submission_date | Jul 18 2013
| | Sample_last_update_date | Aug 03 2013
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_treatment_protocol_ch1 | Sample H295R/TR SF-1 Dox was treated with doxycycline (Dox; 1 ug/mL)
| | Sample_growth_protocol_ch1 | H295R/TR SF-1 cells were grown in DMEM/F12 (Invitrogen) containing antibiotics, 2% NuSerum (BD Biosciences) an 1% ITS+ culture supplement (BD Biosciences) in 6-well plates
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | RNeasy Mini kit (Qiagen) following the manufacturer's procedures
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the GeneChip 3' IVT Express Affymetrix protocol from 2 ug total RNA
| | Sample_hyb_protocol | Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on HG-U133 Plus 2.0 arrays. Arrays were washed and stained in the Affymetrix Fluidics Station 400.
| | Sample_scan_protocol | GeneChips were scanned using the Hewlett-Packard GeneArray Scanner G2500A
| | Sample_data_processing | The data were analyzed with GC-RMA
| | Sample_platform_id | GPL570
| | Sample_contact_name | Enzo,,LALLI
| | Sample_contact_email | ninino@ipmc.cnrs.fr
| | Sample_contact_phone | +33 (0)4 93 95 77 55
| | Sample_contact_laboratory | 402
| | Sample_contact_department | CNRS UMR 7275
| | Sample_contact_institute | IPMC
| | Sample_contact_address | 660 route des Lucioles
| | Sample_contact_city | Valbonne
| | Sample_contact_zip/postal_code | 06560
| | Sample_contact_country | France
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM1192nnn/GSM1192155/suppl/GSM1192155_A856a_01_C_NT_01.CEL.gz
| | Sample_series_id | GSE43032
| | Sample_series_id | GSE43035
| | Sample_data_row_count | 54613
| | |
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GSM1192156 | GPL570 |
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C_NT_02
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H295R/TR SF-1 cells, cultured in basal conditions for 72 hours
|
tissue: adrenal cortex
cell line: H295R/TR SF-1 cell line
treatment: cultured in basal conditions for 72 hours
|
Gene expression data from H295R/TR SF-1 cells cultured in basal conditions for 72 hours
|
| Sample_geo_accession | GSM1192156
| | Sample_status | Public on Aug 01 2013
| | Sample_submission_date | Jul 18 2013
| | Sample_last_update_date | Aug 03 2013
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_treatment_protocol_ch1 | Sample H295R/TR SF-1 Dox was treated with doxycycline (Dox; 1 ug/mL)
| | Sample_growth_protocol_ch1 | H295R/TR SF-1 cells were grown in DMEM/F12 (Invitrogen) containing antibiotics, 2% NuSerum (BD Biosciences) an 1% ITS+ culture supplement (BD Biosciences) in 6-well plates
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | RNeasy Mini kit (Qiagen) following the manufacturer's procedures
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the GeneChip 3' IVT Express Affymetrix protocol from 2 ug total RNA
| | Sample_hyb_protocol | Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on HG-U133 Plus 2.0 arrays. Arrays were washed and stained in the Affymetrix Fluidics Station 400.
| | Sample_scan_protocol | GeneChips were scanned using the Hewlett-Packard GeneArray Scanner G2500A
| | Sample_data_processing | The data were analyzed with GC-RMA
| | Sample_platform_id | GPL570
| | Sample_contact_name | Enzo,,LALLI
| | Sample_contact_email | ninino@ipmc.cnrs.fr
| | Sample_contact_phone | +33 (0)4 93 95 77 55
| | Sample_contact_laboratory | 402
| | Sample_contact_department | CNRS UMR 7275
| | Sample_contact_institute | IPMC
| | Sample_contact_address | 660 route des Lucioles
| | Sample_contact_city | Valbonne
| | Sample_contact_zip/postal_code | 06560
| | Sample_contact_country | France
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM1192nnn/GSM1192156/suppl/GSM1192156_A856a_02_C_NT_02.CEL.gz
| | Sample_series_id | GSE43032
| | Sample_series_id | GSE43035
| | Sample_data_row_count | 54613
| | |
|
GSM1192157 | GPL570 |
|
C_NT_DOX_03
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H295R/TR SF-1 cells, treated with doxycycline (1 ug/mL) for 72 hours
|
tissue: adrenal cortex
cell line: H295R/TR SF-1 cell line
treatment: treated with doxycycline (1 ug/mL) for 72 hours
|
Gene expression data from H295R/TR SF-1 cells treated with doxycycline for 72 hours
|
| Sample_geo_accession | GSM1192157
| | Sample_status | Public on Aug 01 2013
| | Sample_submission_date | Jul 18 2013
| | Sample_last_update_date | Aug 03 2013
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_treatment_protocol_ch1 | Sample H295R/TR SF-1 Dox was treated with doxycycline (Dox; 1 ug/mL)
| | Sample_growth_protocol_ch1 | H295R/TR SF-1 cells were grown in DMEM/F12 (Invitrogen) containing antibiotics, 2% NuSerum (BD Biosciences) an 1% ITS+ culture supplement (BD Biosciences) in 6-well plates
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | RNeasy Mini kit (Qiagen) following the manufacturer's procedures
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the GeneChip 3' IVT Express Affymetrix protocol from 2 ug total RNA
| | Sample_hyb_protocol | Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on HG-U133 Plus 2.0 arrays. Arrays were washed and stained in the Affymetrix Fluidics Station 400.
| | Sample_scan_protocol | GeneChips were scanned using the Hewlett-Packard GeneArray Scanner G2500A
| | Sample_data_processing | The data were analyzed with GC-RMA
| | Sample_platform_id | GPL570
| | Sample_contact_name | Enzo,,LALLI
| | Sample_contact_email | ninino@ipmc.cnrs.fr
| | Sample_contact_phone | +33 (0)4 93 95 77 55
| | Sample_contact_laboratory | 402
| | Sample_contact_department | CNRS UMR 7275
| | Sample_contact_institute | IPMC
| | Sample_contact_address | 660 route des Lucioles
| | Sample_contact_city | Valbonne
| | Sample_contact_zip/postal_code | 06560
| | Sample_contact_country | France
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM1192nnn/GSM1192157/suppl/GSM1192157_A856a_03_C_NT_DOX_03.CEL.gz
| | Sample_series_id | GSE43032
| | Sample_series_id | GSE43035
| | Sample_data_row_count | 54613
| | |
|
GSM1192158 | GPL570 |
|
C_NT_DOX_04
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H295R/TR SF-1 cells, treated with doxycycline (1 ug/mL) for 72 hours
|
tissue: adrenal cortex
cell line: H295R/TR SF-1 cell line
treatment: treated with doxycycline (1 ug/mL) for 72 hours
|
Gene expression data from H295R/TR SF-1 cells treated with doxycycline for 72 hours
|
| Sample_geo_accession | GSM1192158
| | Sample_status | Public on Aug 01 2013
| | Sample_submission_date | Jul 18 2013
| | Sample_last_update_date | Aug 03 2013
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_treatment_protocol_ch1 | Sample H295R/TR SF-1 Dox was treated with doxycycline (Dox; 1 ug/mL)
| | Sample_growth_protocol_ch1 | H295R/TR SF-1 cells were grown in DMEM/F12 (Invitrogen) containing antibiotics, 2% NuSerum (BD Biosciences) an 1% ITS+ culture supplement (BD Biosciences) in 6-well plates
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | RNeasy Mini kit (Qiagen) following the manufacturer's procedures
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the GeneChip 3' IVT Express Affymetrix protocol from 2 ug total RNA
| | Sample_hyb_protocol | Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on HG-U133 Plus 2.0 arrays. Arrays were washed and stained in the Affymetrix Fluidics Station 400.
| | Sample_scan_protocol | GeneChips were scanned using the Hewlett-Packard GeneArray Scanner G2500A
| | Sample_data_processing | The data were analyzed with GC-RMA
| | Sample_platform_id | GPL570
| | Sample_contact_name | Enzo,,LALLI
| | Sample_contact_email | ninino@ipmc.cnrs.fr
| | Sample_contact_phone | +33 (0)4 93 95 77 55
| | Sample_contact_laboratory | 402
| | Sample_contact_department | CNRS UMR 7275
| | Sample_contact_institute | IPMC
| | Sample_contact_address | 660 route des Lucioles
| | Sample_contact_city | Valbonne
| | Sample_contact_zip/postal_code | 06560
| | Sample_contact_country | France
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM1192nnn/GSM1192158/suppl/GSM1192158_A856a_04_C_NT_DOX_04.CEL.gz
| | Sample_series_id | GSE43032
| | Sample_series_id | GSE43035
| | Sample_data_row_count | 54613
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