Search results for the GEO ID: GSE43991 |
(Click on the check boxes provided under "Select for analysis", to initiate grouping) |
(Once the selection is made, click on "Add groups" in "Make groups for comparison", to make a group. Scroll down) |
|
GSM ID | GPL ID |
Select for analysis |
Title |
Source name |
Description |
Characteristics |
GSM1076145 | GPL1261 |
|
non-transformed
|
p53-/- mouse fetal liver progenitor cells
|
cell: p53-/- mouse fetal liver progenitor cells
transformation: non-transformed
|
Gene expression data from the liver progenitor cells
|
Sample_geo_accession | GSM1076145
| Sample_status | Public on Feb 02 2013
| Sample_submission_date | Feb 01 2013
| Sample_last_update_date | Feb 02 2013
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_growth_protocol_ch1 | Liver progenitor cells were cultured in a maintenance medium containing 1:1 DMEM:F12 (GIBCO, Grand Island, NY) with 10% fetal bovine serum (GIBCO) and the following additives: dexamethasone (1×10−7 M; Sigma-Aldrich, St. Louis, MO), nicotinic acid (0.01 M; Sigma-Aldrich), 2-mercaptoethanol (50 mM; Sigma-Aldrich), 1× ITS liquid media supplement (Sigma-Aldrich), EGF (20 ng/ml; R&D Systems, Minneapolis, MN), HGF (50 ng/ml; R&D Systems), and penicillin/streptomycin (1% [v/v]; GIBCO).
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Trizol extraction of total RNA was performed according to the manufacturer's instructions.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 1ug total RNA (Expression Analysis Technical Manual, Affymetrix).
| Sample_hyb_protocol | Following fragmentation, 15 ug of cRNA were hybridized for 16 hr at 45C on GeneChip mouse 430 2.0 Genome Array in the Affymetrix Hybridization Oven 640. GeneChips were washed and stained in the Affymetrix Fluidics Station 450.
| Sample_scan_protocol | GeneChips were scanned using the affymetrix scanner 3000 7G.The scanned images were first assessed by visual inspection then analyzed to generate raw data files saved as CEL files using the default setting of AGCC.
| Sample_data_processing | The data were analyzed with Microarray Suite version 5.0 (MAS 5.0) using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 500.
| Sample_platform_id | GPL1261
| Sample_contact_name | Yongzhong,,Liu
| Sample_contact_email | liuyzg@shsci.org
| Sample_contact_institute | Shanghai Cancer Institute
| Sample_contact_address | Xietu Road 2200, 25
| Sample_contact_city | Shanghai
| Sample_contact_zip/postal_code | 200031
| Sample_contact_country | China
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM1076nnn/GSM1076145/suppl/GSM1076145_non-transformed.CEL.gz
| Sample_series_id | GSE43991
| Sample_data_row_count | 45101
| |
|
GSM1076146 | GPL1261 |
|
H-RasV12
|
p53-/- mouse fetal liver progenitor cells transformed with H-RasV12
|
cell: p53-/- mouse fetal liver progenitor cells transformed with H-RasV12
transformation: H-RasV12
|
Gene expression data from the liver progenitor cells transformed with H-RasV12
|
Sample_geo_accession | GSM1076146
| Sample_status | Public on Feb 02 2013
| Sample_submission_date | Feb 01 2013
| Sample_last_update_date | Feb 02 2013
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_growth_protocol_ch1 | Liver progenitor cells were cultured in a maintenance medium containing 1:1 DMEM:F12 (GIBCO, Grand Island, NY) with 10% fetal bovine serum (GIBCO) and the following additives: dexamethasone (1×10−7 M; Sigma-Aldrich, St. Louis, MO), nicotinic acid (0.01 M; Sigma-Aldrich), 2-mercaptoethanol (50 mM; Sigma-Aldrich), 1× ITS liquid media supplement (Sigma-Aldrich), EGF (20 ng/ml; R&D Systems, Minneapolis, MN), HGF (50 ng/ml; R&D Systems), and penicillin/streptomycin (1% [v/v]; GIBCO).
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Trizol extraction of total RNA was performed according to the manufacturer's instructions.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 1ug total RNA (Expression Analysis Technical Manual, Affymetrix).
| Sample_hyb_protocol | Following fragmentation, 15 ug of cRNA were hybridized for 16 hr at 45C on GeneChip mouse 430 2.0 Genome Array in the Affymetrix Hybridization Oven 640. GeneChips were washed and stained in the Affymetrix Fluidics Station 450.
| Sample_scan_protocol | GeneChips were scanned using the affymetrix scanner 3000 7G.The scanned images were first assessed by visual inspection then analyzed to generate raw data files saved as CEL files using the default setting of AGCC.
| Sample_data_processing | The data were analyzed with Microarray Suite version 5.0 (MAS 5.0) using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 500.
| Sample_platform_id | GPL1261
| Sample_contact_name | Yongzhong,,Liu
| Sample_contact_email | liuyzg@shsci.org
| Sample_contact_institute | Shanghai Cancer Institute
| Sample_contact_address | Xietu Road 2200, 25
| Sample_contact_city | Shanghai
| Sample_contact_zip/postal_code | 200031
| Sample_contact_country | China
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM1076nnn/GSM1076146/suppl/GSM1076146_H-RasV12.CEL.gz
| Sample_series_id | GSE43991
| Sample_data_row_count | 45101
| |
|
GSM1076147 | GPL1261 |
|
myr-Akt
|
p53-/- mouse fetal liver progenitor cells transformed with myr-Akt
|
cell: p53-/- mouse fetal liver progenitor cells transformed with myr-Akt
transformation: myr-Akt
|
Gene expression data from the liver progenitor cells transformed with myr-Akt
|
Sample_geo_accession | GSM1076147
| Sample_status | Public on Feb 02 2013
| Sample_submission_date | Feb 01 2013
| Sample_last_update_date | Feb 02 2013
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_growth_protocol_ch1 | Liver progenitor cells were cultured in a maintenance medium containing 1:1 DMEM:F12 (GIBCO, Grand Island, NY) with 10% fetal bovine serum (GIBCO) and the following additives: dexamethasone (1×10−7 M; Sigma-Aldrich, St. Louis, MO), nicotinic acid (0.01 M; Sigma-Aldrich), 2-mercaptoethanol (50 mM; Sigma-Aldrich), 1× ITS liquid media supplement (Sigma-Aldrich), EGF (20 ng/ml; R&D Systems, Minneapolis, MN), HGF (50 ng/ml; R&D Systems), and penicillin/streptomycin (1% [v/v]; GIBCO).
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Trizol extraction of total RNA was performed according to the manufacturer's instructions.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 1ug total RNA (Expression Analysis Technical Manual, Affymetrix).
| Sample_hyb_protocol | Following fragmentation, 15 ug of cRNA were hybridized for 16 hr at 45C on GeneChip mouse 430 2.0 Genome Array in the Affymetrix Hybridization Oven 640. GeneChips were washed and stained in the Affymetrix Fluidics Station 450.
| Sample_scan_protocol | GeneChips were scanned using the affymetrix scanner 3000 7G.The scanned images were first assessed by visual inspection then analyzed to generate raw data files saved as CEL files using the default setting of AGCC.
| Sample_data_processing | The data were analyzed with Microarray Suite version 5.0 (MAS 5.0) using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 500.
| Sample_platform_id | GPL1261
| Sample_contact_name | Yongzhong,,Liu
| Sample_contact_email | liuyzg@shsci.org
| Sample_contact_institute | Shanghai Cancer Institute
| Sample_contact_address | Xietu Road 2200, 25
| Sample_contact_city | Shanghai
| Sample_contact_zip/postal_code | 200031
| Sample_contact_country | China
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM1076nnn/GSM1076147/suppl/GSM1076147_myr-Akt.CEL.gz
| Sample_series_id | GSE43991
| Sample_data_row_count | 45101
| |
|
GSM1076148 | GPL1261 |
|
c-Myc
|
p53-/- mouse fetal liver progenitor cells transformed with c-Myc
|
cell: p53-/- mouse fetal liver progenitor cells transformed with c-Myc
transformation: c-Myc
|
Gene expression data from the liver progenitor cells transformed with c-Myc
|
Sample_geo_accession | GSM1076148
| Sample_status | Public on Feb 02 2013
| Sample_submission_date | Feb 01 2013
| Sample_last_update_date | Feb 02 2013
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_growth_protocol_ch1 | Liver progenitor cells were cultured in a maintenance medium containing 1:1 DMEM:F12 (GIBCO, Grand Island, NY) with 10% fetal bovine serum (GIBCO) and the following additives: dexamethasone (1×10−7 M; Sigma-Aldrich, St. Louis, MO), nicotinic acid (0.01 M; Sigma-Aldrich), 2-mercaptoethanol (50 mM; Sigma-Aldrich), 1× ITS liquid media supplement (Sigma-Aldrich), EGF (20 ng/ml; R&D Systems, Minneapolis, MN), HGF (50 ng/ml; R&D Systems), and penicillin/streptomycin (1% [v/v]; GIBCO).
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Trizol extraction of total RNA was performed according to the manufacturer's instructions.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 1ug total RNA (Expression Analysis Technical Manual, Affymetrix).
| Sample_hyb_protocol | Following fragmentation, 15 ug of cRNA were hybridized for 16 hr at 45C on GeneChip mouse 430 2.0 Genome Array in the Affymetrix Hybridization Oven 640. GeneChips were washed and stained in the Affymetrix Fluidics Station 450.
| Sample_scan_protocol | GeneChips were scanned using the affymetrix scanner 3000 7G.The scanned images were first assessed by visual inspection then analyzed to generate raw data files saved as CEL files using the default setting of AGCC.
| Sample_data_processing | The data were analyzed with Microarray Suite version 5.0 (MAS 5.0) using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 500.
| Sample_platform_id | GPL1261
| Sample_contact_name | Yongzhong,,Liu
| Sample_contact_email | liuyzg@shsci.org
| Sample_contact_institute | Shanghai Cancer Institute
| Sample_contact_address | Xietu Road 2200, 25
| Sample_contact_city | Shanghai
| Sample_contact_zip/postal_code | 200031
| Sample_contact_country | China
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM1076nnn/GSM1076148/suppl/GSM1076148_c-Myc.CEL.gz
| Sample_series_id | GSE43991
| Sample_data_row_count | 45101
| |
|
|
|
Make groups for comparisons |
(2 groups will be compared at a time) |
|
Select GSMs and click on "Add groups" |
Enter the group name here: |
|
|
|