Search results for the GEO ID: GSE18991 |
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|
GSM ID | GPL ID |
Select for analysis |
Title |
Source name |
Description |
Characteristics |
GSM469866 | GPL1261 |
|
chondrocytes at E18.5, control, biological rep1
|
Mouse rib chondrocytes
|
strain: FVB
age: E18.5
tissue: primary chondrocytes
genome/variation: wild type
|
Mouse_270TA
|
Sample_geo_accession | GSM469866
| Sample_status | Public on Oct 15 2010
| Sample_submission_date | Nov 12 2009
| Sample_last_update_date | Nov 12 2009
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | Rib cages were dissected from E18.5 embryos and washed in PBS. Cells were dissociated by enzymatic digestion with 0.25% Collagenase and 0.25% Trypsin/EDTA for 1h at 37oC. The rib cages were washed, and fresh 0.25% Collagenase in PBS was added for 1h at 37oC. Enzymatic reaction was stopped by adding an equal volume of tissue culture medium containing 10% FCS. The cells were filtered through a 70 micrometer cell strainer and pelleted (1200rpm for 10min). Pellets were washed with PBS and stored in Trizol reagent.
| Sample_growth_protocol_ch1 | Pregnant dams were single housed, the morning with presence of a vaginal plug being counted as 0.5 days.
| 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 | Biotin-labeled samples were generated using the Affymetrix Eukaryotic One-Cycle Target Labeling Assay.
| Sample_hyb_protocol | GeneChip arrays were hybridized overnight in the Affymetrix hybridization oven at 42oC. Washing and scanning was performed using the Affymetrix GeneChip Fluidics Station 450.
| Sample_scan_protocol | GeneChips were scanned using the GeneChip Scanner 3000 7G.
| 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.
| Sample_platform_id | GPL1261
| Sample_contact_name | Claudia,,Kappen
| Sample_contact_email | claudia.kappen@pbrc.edu
| Sample_contact_phone | 225-763-2781
| Sample_contact_department | Developmental Biology
| Sample_contact_institute | Pennington Biomedical Research Center
| Sample_contact_address | 6400 Perkins Road
| Sample_contact_city | Baton Rouge
| Sample_contact_state | LA
| Sample_contact_zip/postal_code | 70808
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM469nnn/GSM469866/suppl/GSM469866.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM469nnn/GSM469866/suppl/GSM469866.CHP.gz
| Sample_series_id | GSE18991
| Sample_series_id | GSE19002
| Sample_data_row_count | 45101
| |
|
GSM469867 | GPL1261 |
|
chondrocytes at E18.5, control, biological rep2
|
Mouse rib chondrocytes
|
strain: FVB
age: E18.5
tissue: primary chondrocytes
genome/variation: wild type
|
Mouse_271TA
|
Sample_geo_accession | GSM469867
| Sample_status | Public on Oct 15 2010
| Sample_submission_date | Nov 12 2009
| Sample_last_update_date | Nov 12 2009
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | Rib cages were dissected from E18.5 embryos and washed in PBS. Cells were dissociated by enzymatic digestion with 0.25% Collagenase and 0.25% Trypsin/EDTA for 1h at 37oC. The rib cages were washed, and fresh 0.25% Collagenase in PBS was added for 1h at 37oC. Enzymatic reaction was stopped by adding an equal volume of tissue culture medium containing 10% FCS. The cells were filtered through a 70 micrometer cell strainer and pelleted (1200rpm for 10min). Pellets were washed with PBS and stored in Trizol reagent.
| Sample_growth_protocol_ch1 | Pregnant dams were single housed, the morning with presence of a vaginal plug being counted as 0.5 days.
| 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 | Biotin-labeled samples were generated using the Affymetrix Eukaryotic One-Cycle Target Labeling Assay.
| Sample_hyb_protocol | GeneChip arrays were hybridized overnight in the Affymetrix hybridization oven at 42oC. Washing and scanning was performed using the Affymetrix GeneChip Fluidics Station 450.
| Sample_scan_protocol | GeneChips were scanned using the GeneChip Scanner 3000 7G.
| 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.
| Sample_platform_id | GPL1261
| Sample_contact_name | Claudia,,Kappen
| Sample_contact_email | claudia.kappen@pbrc.edu
| Sample_contact_phone | 225-763-2781
| Sample_contact_department | Developmental Biology
| Sample_contact_institute | Pennington Biomedical Research Center
| Sample_contact_address | 6400 Perkins Road
| Sample_contact_city | Baton Rouge
| Sample_contact_state | LA
| Sample_contact_zip/postal_code | 70808
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM469nnn/GSM469867/suppl/GSM469867.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM469nnn/GSM469867/suppl/GSM469867.CHP.gz
| Sample_series_id | GSE18991
| Sample_series_id | GSE19002
| Sample_data_row_count | 45101
| |
|
GSM469868 | GPL1261 |
|
chondrocytes at E18.5, control, biological rep3
|
Mouse rib chondrocytes
|
strain: FVB
age: E18.5
tissue: primary chondrocytes
genome/variation: wild type
|
Mouse_273TA
|
Sample_geo_accession | GSM469868
| Sample_status | Public on Oct 15 2010
| Sample_submission_date | Nov 12 2009
| Sample_last_update_date | Nov 12 2009
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | Rib cages were dissected from E18.5 embryos and washed in PBS. Cells were dissociated by enzymatic digestion with 0.25% Collagenase and 0.25% Trypsin/EDTA for 1h at 37oC. The rib cages were washed, and fresh 0.25% Collagenase in PBS was added for 1h at 37oC. Enzymatic reaction was stopped by adding an equal volume of tissue culture medium containing 10% FCS. The cells were filtered through a 70 micrometer cell strainer and pelleted (1200rpm for 10min). Pellets were washed with PBS and stored in Trizol reagent.
| Sample_growth_protocol_ch1 | Pregnant dams were single housed, the morning with presence of a vaginal plug being counted as 0.5 days.
| 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 | Biotin-labeled samples were generated using the Affymetrix Eukaryotic One-Cycle Target Labeling Assay.
| Sample_hyb_protocol | GeneChip arrays were hybridized overnight in the Affymetrix hybridization oven at 42oC. Washing and scanning was performed using the Affymetrix GeneChip Fluidics Station 450.
| Sample_scan_protocol | GeneChips were scanned using the GeneChip Scanner 3000 7G.
| 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.
| Sample_platform_id | GPL1261
| Sample_contact_name | Claudia,,Kappen
| Sample_contact_email | claudia.kappen@pbrc.edu
| Sample_contact_phone | 225-763-2781
| Sample_contact_department | Developmental Biology
| Sample_contact_institute | Pennington Biomedical Research Center
| Sample_contact_address | 6400 Perkins Road
| Sample_contact_city | Baton Rouge
| Sample_contact_state | LA
| Sample_contact_zip/postal_code | 70808
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM469nnn/GSM469868/suppl/GSM469868.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM469nnn/GSM469868/suppl/GSM469868.CHP.gz
| Sample_series_id | GSE18991
| Sample_series_id | GSE19002
| Sample_data_row_count | 45101
| |
|
GSM469869 | GPL1261 |
|
chondrocytes at E18.5, control, biological rep4
|
Mouse rib chondrocytes
|
strain: FVB
age: E18.5
tissue: primary chondrocytes
genome/variation: wild type
|
Mouse_291TA
|
Sample_geo_accession | GSM469869
| Sample_status | Public on Oct 15 2010
| Sample_submission_date | Nov 12 2009
| Sample_last_update_date | Nov 12 2009
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | Rib cages were dissected from E18.5 embryos and washed in PBS. Cells were dissociated by enzymatic digestion with 0.25% Collagenase and 0.25% Trypsin/EDTA for 1h at 37oC. The rib cages were washed, and fresh 0.25% Collagenase in PBS was added for 1h at 37oC. Enzymatic reaction was stopped by adding an equal volume of tissue culture medium containing 10% FCS. The cells were filtered through a 70 micrometer cell strainer and pelleted (1200rpm for 10min). Pellets were washed with PBS and stored in Trizol reagent.
| Sample_growth_protocol_ch1 | Pregnant dams were single housed, the morning with presence of a vaginal plug being counted as 0.5 days.
| 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 | Biotin-labeled samples were generated using the Affymetrix Eukaryotic One-Cycle Target Labeling Assay.
| Sample_hyb_protocol | GeneChip arrays were hybridized overnight in the Affymetrix hybridization oven at 42oC. Washing and scanning was performed using the Affymetrix GeneChip Fluidics Station 450.
| Sample_scan_protocol | GeneChips were scanned using the GeneChip Scanner 3000 7G.
| 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.
| Sample_platform_id | GPL1261
| Sample_contact_name | Claudia,,Kappen
| Sample_contact_email | claudia.kappen@pbrc.edu
| Sample_contact_phone | 225-763-2781
| Sample_contact_department | Developmental Biology
| Sample_contact_institute | Pennington Biomedical Research Center
| Sample_contact_address | 6400 Perkins Road
| Sample_contact_city | Baton Rouge
| Sample_contact_state | LA
| Sample_contact_zip/postal_code | 70808
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM469nnn/GSM469869/suppl/GSM469869.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM469nnn/GSM469869/suppl/GSM469869.CHP.gz
| Sample_series_id | GSE18991
| Sample_series_id | GSE19002
| Sample_data_row_count | 45101
| |
|
GSM469870 | GPL1261 |
|
chondrocytes at E18.5, transgenic, biological rep1
|
Mouse rib chondrocytes
|
strain: FVB
age: E18.5
tissue: primary chondrocytes
genome/variation: Hoxd4 transgenic
|
Mouse_270TR
|
Sample_geo_accession | GSM469870
| Sample_status | Public on Oct 15 2010
| Sample_submission_date | Nov 12 2009
| Sample_last_update_date | Nov 12 2009
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | Rib cages were dissected from E18.5 embryos and washed in PBS. Cells were dissociated by enzymatic digestion with 0.25% Collagenase and 0.25% Trypsin/EDTA for 1h at 37oC. The rib cages were washed, and fresh 0.25% Collagenase in PBS was added for 1h at 37oC. Enzymatic reaction was stopped by adding an equal volume of tissue culture medium containing 10% FCS. The cells were filtered through a 70 micrometer cell strainer and pelleted (1200rpm for 10min). Pellets were washed with PBS and stored in Trizol reagent.
| Sample_growth_protocol_ch1 | Pregnant dams were single housed, the morning with presence of a vaginal plug being counted as 0.5 days.
| 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 | Biotin-labeled samples were generated using the Affymetrix Eukaryotic One-Cycle Target Labeling Assay.
| Sample_hyb_protocol | GeneChip arrays were hybridized overnight in the Affymetrix hybridization oven at 42oC. Washing and scanning was performed using the Affymetrix GeneChip Fluidics Station 450.
| Sample_scan_protocol | GeneChips were scanned using the GeneChip Scanner 3000 7G.
| 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.
| Sample_platform_id | GPL1261
| Sample_contact_name | Claudia,,Kappen
| Sample_contact_email | claudia.kappen@pbrc.edu
| Sample_contact_phone | 225-763-2781
| Sample_contact_department | Developmental Biology
| Sample_contact_institute | Pennington Biomedical Research Center
| Sample_contact_address | 6400 Perkins Road
| Sample_contact_city | Baton Rouge
| Sample_contact_state | LA
| Sample_contact_zip/postal_code | 70808
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM469nnn/GSM469870/suppl/GSM469870.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM469nnn/GSM469870/suppl/GSM469870.CHP.gz
| Sample_series_id | GSE18991
| Sample_series_id | GSE19002
| Sample_data_row_count | 45101
| |
|
GSM469871 | GPL1261 |
|
chondrocytes at E18.5, transgenic, biological rep2
|
Mouse rib chondrocytes
|
strain: FVB
age: E18.5
tissue: primary chondrocytes
genome/variation: Hoxd4 transgenic
|
Mouse_271TR
|
Sample_geo_accession | GSM469871
| Sample_status | Public on Oct 15 2010
| Sample_submission_date | Nov 12 2009
| Sample_last_update_date | Nov 12 2009
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | Rib cages were dissected from E18.5 embryos and washed in PBS. Cells were dissociated by enzymatic digestion with 0.25% Collagenase and 0.25% Trypsin/EDTA for 1h at 37oC. The rib cages were washed, and fresh 0.25% Collagenase in PBS was added for 1h at 37oC. Enzymatic reaction was stopped by adding an equal volume of tissue culture medium containing 10% FCS. The cells were filtered through a 70 micrometer cell strainer and pelleted (1200rpm for 10min). Pellets were washed with PBS and stored in Trizol reagent.
| Sample_growth_protocol_ch1 | Pregnant dams were single housed, the morning with presence of a vaginal plug being counted as 0.5 days.
| 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 | Biotin-labeled samples were generated using the Affymetrix Eukaryotic One-Cycle Target Labeling Assay.
| Sample_hyb_protocol | GeneChip arrays were hybridized overnight in the Affymetrix hybridization oven at 42oC. Washing and scanning was performed using the Affymetrix GeneChip Fluidics Station 450.
| Sample_scan_protocol | GeneChips were scanned using the GeneChip Scanner 3000 7G.
| 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.
| Sample_platform_id | GPL1261
| Sample_contact_name | Claudia,,Kappen
| Sample_contact_email | claudia.kappen@pbrc.edu
| Sample_contact_phone | 225-763-2781
| Sample_contact_department | Developmental Biology
| Sample_contact_institute | Pennington Biomedical Research Center
| Sample_contact_address | 6400 Perkins Road
| Sample_contact_city | Baton Rouge
| Sample_contact_state | LA
| Sample_contact_zip/postal_code | 70808
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM469nnn/GSM469871/suppl/GSM469871.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM469nnn/GSM469871/suppl/GSM469871.CHP.gz
| Sample_series_id | GSE18991
| Sample_series_id | GSE19002
| Sample_data_row_count | 45101
| |
|
GSM469872 | GPL1261 |
|
chondrocytes at E18.5, transgenic, biological rep3
|
Mouse rib chondrocytes
|
strain: FVB
age: E18.5
tissue: primary chondrocytes
genome/variation: Hoxd4 transgenic
|
Mouse_273TR
|
Sample_geo_accession | GSM469872
| Sample_status | Public on Oct 15 2010
| Sample_submission_date | Nov 12 2009
| Sample_last_update_date | Nov 12 2009
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | Rib cages were dissected from E18.5 embryos and washed in PBS. Cells were dissociated by enzymatic digestion with 0.25% Collagenase and 0.25% Trypsin/EDTA for 1h at 37oC. The rib cages were washed, and fresh 0.25% Collagenase in PBS was added for 1h at 37oC. Enzymatic reaction was stopped by adding an equal volume of tissue culture medium containing 10% FCS. The cells were filtered through a 70 micrometer cell strainer and pelleted (1200rpm for 10min). Pellets were washed with PBS and stored in Trizol reagent.
| Sample_growth_protocol_ch1 | Pregnant dams were single housed, the morning with presence of a vaginal plug being counted as 0.5 days.
| 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 | Biotin-labeled samples were generated using the Affymetrix Eukaryotic One-Cycle Target Labeling Assay.
| Sample_hyb_protocol | GeneChip arrays were hybridized overnight in the Affymetrix hybridization oven at 42oC. Washing and scanning was performed using the Affymetrix GeneChip Fluidics Station 450.
| Sample_scan_protocol | GeneChips were scanned using the GeneChip Scanner 3000 7G.
| 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.
| Sample_platform_id | GPL1261
| Sample_contact_name | Claudia,,Kappen
| Sample_contact_email | claudia.kappen@pbrc.edu
| Sample_contact_phone | 225-763-2781
| Sample_contact_department | Developmental Biology
| Sample_contact_institute | Pennington Biomedical Research Center
| Sample_contact_address | 6400 Perkins Road
| Sample_contact_city | Baton Rouge
| Sample_contact_state | LA
| Sample_contact_zip/postal_code | 70808
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM469nnn/GSM469872/suppl/GSM469872.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM469nnn/GSM469872/suppl/GSM469872.CHP.gz
| Sample_series_id | GSE18991
| Sample_series_id | GSE19002
| Sample_data_row_count | 45101
| |
|
GSM469873 | GPL1261 |
|
chondrocytes at E18.5, transgenic, biological rep4
|
Mouse rib chondrocytes
|
strain: FVB
age: E18.5
tissue: primary chondrocytes
genome/variation: Hoxd4 transgenic
|
Mouse_291TR
|
Sample_geo_accession | GSM469873
| Sample_status | Public on Oct 15 2010
| Sample_submission_date | Nov 12 2009
| Sample_last_update_date | Nov 12 2009
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | Rib cages were dissected from E18.5 embryos and washed in PBS. Cells were dissociated by enzymatic digestion with 0.25% Collagenase and 0.25% Trypsin/EDTA for 1h at 37oC. The rib cages were washed, and fresh 0.25% Collagenase in PBS was added for 1h at 37oC. Enzymatic reaction was stopped by adding an equal volume of tissue culture medium containing 10% FCS. The cells were filtered through a 70 micrometer cell strainer and pelleted (1200rpm for 10min). Pellets were washed with PBS and stored in Trizol reagent.
| Sample_growth_protocol_ch1 | Pregnant dams were single housed, the morning with presence of a vaginal plug being counted as 0.5 days.
| 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 | Biotin-labeled samples were generated using the Affymetrix Eukaryotic One-Cycle Target Labeling Assay.
| Sample_hyb_protocol | GeneChip arrays were hybridized overnight in the Affymetrix hybridization oven at 42oC. Washing and scanning was performed using the Affymetrix GeneChip Fluidics Station 450.
| Sample_scan_protocol | GeneChips were scanned using the GeneChip Scanner 3000 7G.
| 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.
| Sample_platform_id | GPL1261
| Sample_contact_name | Claudia,,Kappen
| Sample_contact_email | claudia.kappen@pbrc.edu
| Sample_contact_phone | 225-763-2781
| Sample_contact_department | Developmental Biology
| Sample_contact_institute | Pennington Biomedical Research Center
| Sample_contact_address | 6400 Perkins Road
| Sample_contact_city | Baton Rouge
| Sample_contact_state | LA
| Sample_contact_zip/postal_code | 70808
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM469nnn/GSM469873/suppl/GSM469873.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM469nnn/GSM469873/suppl/GSM469873.CHP.gz
| Sample_series_id | GSE18991
| Sample_series_id | GSE19002
| Sample_data_row_count | 45101
| |
|
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