Search results for the GEO ID: GSE9171 |
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|
GSM ID | GPL ID |
Select for analysis |
Title |
Source name |
Description |
Characteristics |
GSM231695 | GPL570 |
|
Glioblastoma tumor GBM_157
|
human glioblastoma tumor
|
Human glioblastoma tumor
|
Gene expression data from human glioblastoma tumor.
|
Sample_geo_accession | GSM231695
| Sample_status | Public on Apr 29 2008
| Sample_submission_date | Sep 26 2007
| Sample_last_update_date | Aug 14 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| 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 15 microg total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| Sample_hyb_protocol | Following fragmentation, cRNA were hybridized for 16 hr at 45C on GeneChip Human Genome U133Plus2.0. The chips are then transferred to a fluidics instrument that performs washes to remove cRNA that has not hybridized to its complementary oligonucleotide probe. The bound cRNA is then fluorescently labeled using phycoerythrin-conjugated streptavidin (SAPE); additional fluors are then added using biotinylated anti-streptavidin antibody and additional SAPE.
| Sample_scan_protocol | Each cRNA bound at its complementary oligonucleotide is excited using a confocal laser scanner, and the positions and intensities of the fluorescent emissions are captured.
| 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 100.
| Sample_platform_id | GPL570
| Sample_contact_name | Yonghong,,Xiao
| Sample_contact_email | yonghong_xiao@yahoo.com
| Sample_contact_institute | Dana-Farber Cancer Institute
| Sample_contact_address | 450 Brookline Ave., HIM218A
| Sample_contact_city | Boston
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02115
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM231nnn/GSM231695/suppl/GSM231695.CEL.gz
| Sample_series_id | GSE9171
| Sample_series_id | GSE9200
| Sample_data_row_count | 54675
| |
|
GSM231696 | GPL570 |
|
Glioblastoma tumor GBM_186
|
human glioblastoma tumor
|
Human glioblastoma tumor
|
Gene expression data from human glioblastoma tumor.
|
Sample_geo_accession | GSM231696
| Sample_status | Public on Apr 29 2008
| Sample_submission_date | Sep 26 2007
| Sample_last_update_date | Aug 14 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| 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 15 microg total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| Sample_hyb_protocol | Following fragmentation, cRNA were hybridized for 16 hr at 45C on GeneChip Human Genome U133Plus2.0. The chips are then transferred to a fluidics instrument that performs washes to remove cRNA that has not hybridized to its complementary oligonucleotide probe. The bound cRNA is then fluorescently labeled using phycoerythrin-conjugated streptavidin (SAPE); additional fluors are then added using biotinylated anti-streptavidin antibody and additional SAPE.
| Sample_scan_protocol | Each cRNA bound at its complementary oligonucleotide is excited using a confocal laser scanner, and the positions and intensities of the fluorescent emissions are captured.
| 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 100.
| Sample_platform_id | GPL570
| Sample_contact_name | Yonghong,,Xiao
| Sample_contact_email | yonghong_xiao@yahoo.com
| Sample_contact_institute | Dana-Farber Cancer Institute
| Sample_contact_address | 450 Brookline Ave., HIM218A
| Sample_contact_city | Boston
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02115
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM231nnn/GSM231696/suppl/GSM231696.CEL.gz
| Sample_series_id | GSE9171
| Sample_series_id | GSE9200
| Sample_data_row_count | 54675
| |
|
GSM231697 | GPL570 |
|
Glioblastoma tumor GBM_193
|
human glioblastoma tumor
|
Human glioblastoma tumor
|
Gene expression data from human glioblastoma tumor.
|
Sample_geo_accession | GSM231697
| Sample_status | Public on Apr 29 2008
| Sample_submission_date | Sep 26 2007
| Sample_last_update_date | Aug 14 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| 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 15 microg total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| Sample_hyb_protocol | Following fragmentation, cRNA were hybridized for 16 hr at 45C on GeneChip Human Genome U133Plus2.0. The chips are then transferred to a fluidics instrument that performs washes to remove cRNA that has not hybridized to its complementary oligonucleotide probe. The bound cRNA is then fluorescently labeled using phycoerythrin-conjugated streptavidin (SAPE); additional fluors are then added using biotinylated anti-streptavidin antibody and additional SAPE.
| Sample_scan_protocol | Each cRNA bound at its complementary oligonucleotide is excited using a confocal laser scanner, and the positions and intensities of the fluorescent emissions are captured.
| 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 100.
| Sample_platform_id | GPL570
| Sample_contact_name | Yonghong,,Xiao
| Sample_contact_email | yonghong_xiao@yahoo.com
| Sample_contact_institute | Dana-Farber Cancer Institute
| Sample_contact_address | 450 Brookline Ave., HIM218A
| Sample_contact_city | Boston
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02115
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM231nnn/GSM231697/suppl/GSM231697.CEL.gz
| Sample_series_id | GSE9171
| Sample_series_id | GSE9200
| Sample_data_row_count | 54675
| |
|
GSM231698 | GPL570 |
|
Glioblastoma tumor GBM_199
|
human glioblastoma tumor
|
Human glioblastoma tumor
|
Gene expression data from human glioblastoma tumor.
|
Sample_geo_accession | GSM231698
| Sample_status | Public on Apr 29 2008
| Sample_submission_date | Sep 26 2007
| Sample_last_update_date | Aug 14 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| 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 15 microg total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| Sample_hyb_protocol | Following fragmentation, cRNA were hybridized for 16 hr at 45C on GeneChip Human Genome U133Plus2.0. The chips are then transferred to a fluidics instrument that performs washes to remove cRNA that has not hybridized to its complementary oligonucleotide probe. The bound cRNA is then fluorescently labeled using phycoerythrin-conjugated streptavidin (SAPE); additional fluors are then added using biotinylated anti-streptavidin antibody and additional SAPE.
| Sample_scan_protocol | Each cRNA bound at its complementary oligonucleotide is excited using a confocal laser scanner, and the positions and intensities of the fluorescent emissions are captured.
| 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 100.
| Sample_platform_id | GPL570
| Sample_contact_name | Yonghong,,Xiao
| Sample_contact_email | yonghong_xiao@yahoo.com
| Sample_contact_institute | Dana-Farber Cancer Institute
| Sample_contact_address | 450 Brookline Ave., HIM218A
| Sample_contact_city | Boston
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02115
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM231nnn/GSM231698/suppl/GSM231698.CEL.gz
| Sample_series_id | GSE9171
| Sample_series_id | GSE9200
| Sample_data_row_count | 54675
| |
|
GSM231699 | GPL570 |
|
Glioblastoma tumor GBM_206
|
human glioblastoma tumor
|
Human glioblastoma tumor
|
Gene expression data from human glioblastoma tumor.
|
Sample_geo_accession | GSM231699
| Sample_status | Public on Apr 29 2008
| Sample_submission_date | Sep 26 2007
| Sample_last_update_date | Aug 14 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| 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 15 microg total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| Sample_hyb_protocol | Following fragmentation, cRNA were hybridized for 16 hr at 45C on GeneChip Human Genome U133Plus2.0. The chips are then transferred to a fluidics instrument that performs washes to remove cRNA that has not hybridized to its complementary oligonucleotide probe. The bound cRNA is then fluorescently labeled using phycoerythrin-conjugated streptavidin (SAPE); additional fluors are then added using biotinylated anti-streptavidin antibody and additional SAPE.
| Sample_scan_protocol | Each cRNA bound at its complementary oligonucleotide is excited using a confocal laser scanner, and the positions and intensities of the fluorescent emissions are captured.
| 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 100.
| Sample_platform_id | GPL570
| Sample_contact_name | Yonghong,,Xiao
| Sample_contact_email | yonghong_xiao@yahoo.com
| Sample_contact_institute | Dana-Farber Cancer Institute
| Sample_contact_address | 450 Brookline Ave., HIM218A
| Sample_contact_city | Boston
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02115
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM231nnn/GSM231699/suppl/GSM231699.CEL.gz
| Sample_series_id | GSE9171
| Sample_series_id | GSE9200
| Sample_data_row_count | 54675
| |
|
GSM231700 | GPL570 |
|
Glioblastoma tumor GBM_210
|
human glioblastoma tumor
|
Human glioblastoma tumor
|
Gene expression data from human glioblastoma tumor.
|
Sample_geo_accession | GSM231700
| Sample_status | Public on Apr 29 2008
| Sample_submission_date | Sep 26 2007
| Sample_last_update_date | Aug 14 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| 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 15 microg total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| Sample_hyb_protocol | Following fragmentation, cRNA were hybridized for 16 hr at 45C on GeneChip Human Genome U133Plus2.0. The chips are then transferred to a fluidics instrument that performs washes to remove cRNA that has not hybridized to its complementary oligonucleotide probe. The bound cRNA is then fluorescently labeled using phycoerythrin-conjugated streptavidin (SAPE); additional fluors are then added using biotinylated anti-streptavidin antibody and additional SAPE.
| Sample_scan_protocol | Each cRNA bound at its complementary oligonucleotide is excited using a confocal laser scanner, and the positions and intensities of the fluorescent emissions are captured.
| 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 100.
| Sample_platform_id | GPL570
| Sample_contact_name | Yonghong,,Xiao
| Sample_contact_email | yonghong_xiao@yahoo.com
| Sample_contact_institute | Dana-Farber Cancer Institute
| Sample_contact_address | 450 Brookline Ave., HIM218A
| Sample_contact_city | Boston
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02115
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM231nnn/GSM231700/suppl/GSM231700.CEL.gz
| Sample_series_id | GSE9171
| Sample_series_id | GSE9200
| Sample_data_row_count | 54675
| |
|
GSM231701 | GPL570 |
|
Glioblastoma tumor GBM_218
|
human glioblastoma tumor
|
Human glioblastoma tumor
|
Gene expression data from human glioblastoma tumor.
|
Sample_geo_accession | GSM231701
| Sample_status | Public on Apr 29 2008
| Sample_submission_date | Sep 26 2007
| Sample_last_update_date | Aug 14 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| 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 15 microg total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| Sample_hyb_protocol | Following fragmentation, cRNA were hybridized for 16 hr at 45C on GeneChip Human Genome U133Plus2.0. The chips are then transferred to a fluidics instrument that performs washes to remove cRNA that has not hybridized to its complementary oligonucleotide probe. The bound cRNA is then fluorescently labeled using phycoerythrin-conjugated streptavidin (SAPE); additional fluors are then added using biotinylated anti-streptavidin antibody and additional SAPE.
| Sample_scan_protocol | Each cRNA bound at its complementary oligonucleotide is excited using a confocal laser scanner, and the positions and intensities of the fluorescent emissions are captured.
| 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 100.
| Sample_platform_id | GPL570
| Sample_contact_name | Yonghong,,Xiao
| Sample_contact_email | yonghong_xiao@yahoo.com
| Sample_contact_institute | Dana-Farber Cancer Institute
| Sample_contact_address | 450 Brookline Ave., HIM218A
| Sample_contact_city | Boston
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02115
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM231nnn/GSM231701/suppl/GSM231701.CEL.gz
| Sample_series_id | GSE9171
| Sample_series_id | GSE9200
| Sample_data_row_count | 54675
| |
|
GSM231702 | GPL570 |
|
Glioblastoma tumor GBM_257
|
human glioblastoma tumor
|
Human glioblastoma tumor
|
Gene expression data from human glioblastoma tumor.
|
Sample_geo_accession | GSM231702
| Sample_status | Public on Apr 29 2008
| Sample_submission_date | Sep 26 2007
| Sample_last_update_date | Aug 14 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| 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 15 microg total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| Sample_hyb_protocol | Following fragmentation, cRNA were hybridized for 16 hr at 45C on GeneChip Human Genome U133Plus2.0. The chips are then transferred to a fluidics instrument that performs washes to remove cRNA that has not hybridized to its complementary oligonucleotide probe. The bound cRNA is then fluorescently labeled using phycoerythrin-conjugated streptavidin (SAPE); additional fluors are then added using biotinylated anti-streptavidin antibody and additional SAPE.
| Sample_scan_protocol | Each cRNA bound at its complementary oligonucleotide is excited using a confocal laser scanner, and the positions and intensities of the fluorescent emissions are captured.
| 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 100.
| Sample_platform_id | GPL570
| Sample_contact_name | Yonghong,,Xiao
| Sample_contact_email | yonghong_xiao@yahoo.com
| Sample_contact_institute | Dana-Farber Cancer Institute
| Sample_contact_address | 450 Brookline Ave., HIM218A
| Sample_contact_city | Boston
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02115
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM231nnn/GSM231702/suppl/GSM231702.CEL.gz
| Sample_series_id | GSE9171
| Sample_series_id | GSE9200
| Sample_data_row_count | 54675
| |
|
GSM231703 | GPL570 |
|
Glioblastoma tumor GBM_271
|
human glioblastoma tumor
|
Human glioblastoma tumor
|
Gene expression data from human glioblastoma tumor.
|
Sample_geo_accession | GSM231703
| Sample_status | Public on Apr 29 2008
| Sample_submission_date | Sep 26 2007
| Sample_last_update_date | Aug 14 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| 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 15 microg total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| Sample_hyb_protocol | Following fragmentation, cRNA were hybridized for 16 hr at 45C on GeneChip Human Genome U133Plus2.0. The chips are then transferred to a fluidics instrument that performs washes to remove cRNA that has not hybridized to its complementary oligonucleotide probe. The bound cRNA is then fluorescently labeled using phycoerythrin-conjugated streptavidin (SAPE); additional fluors are then added using biotinylated anti-streptavidin antibody and additional SAPE.
| Sample_scan_protocol | Each cRNA bound at its complementary oligonucleotide is excited using a confocal laser scanner, and the positions and intensities of the fluorescent emissions are captured.
| 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 100.
| Sample_platform_id | GPL570
| Sample_contact_name | Yonghong,,Xiao
| Sample_contact_email | yonghong_xiao@yahoo.com
| Sample_contact_institute | Dana-Farber Cancer Institute
| Sample_contact_address | 450 Brookline Ave., HIM218A
| Sample_contact_city | Boston
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02115
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM231nnn/GSM231703/suppl/GSM231703.CEL.gz
| Sample_series_id | GSE9171
| Sample_series_id | GSE9200
| Sample_data_row_count | 54675
| |
|
GSM231704 | GPL570 |
|
Glioblastoma tumor GBM_311
|
human glioblastoma tumor
|
Human glioblastoma tumor
|
Gene expression data from human glioblastoma tumor.
|
Sample_geo_accession | GSM231704
| Sample_status | Public on Apr 29 2008
| Sample_submission_date | Sep 26 2007
| Sample_last_update_date | Aug 14 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| 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 15 microg total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| Sample_hyb_protocol | Following fragmentation, cRNA were hybridized for 16 hr at 45C on GeneChip Human Genome U133Plus2.0. The chips are then transferred to a fluidics instrument that performs washes to remove cRNA that has not hybridized to its complementary oligonucleotide probe. The bound cRNA is then fluorescently labeled using phycoerythrin-conjugated streptavidin (SAPE); additional fluors are then added using biotinylated anti-streptavidin antibody and additional SAPE.
| Sample_scan_protocol | Each cRNA bound at its complementary oligonucleotide is excited using a confocal laser scanner, and the positions and intensities of the fluorescent emissions are captured.
| 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 100.
| Sample_platform_id | GPL570
| Sample_contact_name | Yonghong,,Xiao
| Sample_contact_email | yonghong_xiao@yahoo.com
| Sample_contact_institute | Dana-Farber Cancer Institute
| Sample_contact_address | 450 Brookline Ave., HIM218A
| Sample_contact_city | Boston
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02115
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM231nnn/GSM231704/suppl/GSM231704.CEL.gz
| Sample_series_id | GSE9171
| Sample_series_id | GSE9200
| Sample_data_row_count | 54675
| |
|
GSM231705 | GPL570 |
|
Glioblastoma tumor GBM_328
|
human glioblastoma tumor
|
Human glioblastoma tumor
|
Gene expression data from human glioblastoma tumor.
|
Sample_geo_accession | GSM231705
| Sample_status | Public on Apr 29 2008
| Sample_submission_date | Sep 26 2007
| Sample_last_update_date | Aug 14 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| 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 15 microg total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| Sample_hyb_protocol | Following fragmentation, cRNA were hybridized for 16 hr at 45C on GeneChip Human Genome U133Plus2.0. The chips are then transferred to a fluidics instrument that performs washes to remove cRNA that has not hybridized to its complementary oligonucleotide probe. The bound cRNA is then fluorescently labeled using phycoerythrin-conjugated streptavidin (SAPE); additional fluors are then added using biotinylated anti-streptavidin antibody and additional SAPE.
| Sample_scan_protocol | Each cRNA bound at its complementary oligonucleotide is excited using a confocal laser scanner, and the positions and intensities of the fluorescent emissions are captured.
| 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 100.
| Sample_platform_id | GPL570
| Sample_contact_name | Yonghong,,Xiao
| Sample_contact_email | yonghong_xiao@yahoo.com
| Sample_contact_institute | Dana-Farber Cancer Institute
| Sample_contact_address | 450 Brookline Ave., HIM218A
| Sample_contact_city | Boston
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02115
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM231nnn/GSM231705/suppl/GSM231705.CEL.gz
| Sample_series_id | GSE9171
| Sample_series_id | GSE9200
| Sample_data_row_count | 54675
| |
|
GSM231706 | GPL570 |
|
Glioblastoma tumor GBM_349
|
human glioblastoma tumor
|
Human glioblastoma tumor
|
Gene expression data from human glioblastoma tumor.
|
Sample_geo_accession | GSM231706
| Sample_status | Public on Apr 29 2008
| Sample_submission_date | Sep 26 2007
| Sample_last_update_date | Aug 14 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| 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 15 microg total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| Sample_hyb_protocol | Following fragmentation, cRNA were hybridized for 16 hr at 45C on GeneChip Human Genome U133Plus2.0. The chips are then transferred to a fluidics instrument that performs washes to remove cRNA that has not hybridized to its complementary oligonucleotide probe. The bound cRNA is then fluorescently labeled using phycoerythrin-conjugated streptavidin (SAPE); additional fluors are then added using biotinylated anti-streptavidin antibody and additional SAPE.
| Sample_scan_protocol | Each cRNA bound at its complementary oligonucleotide is excited using a confocal laser scanner, and the positions and intensities of the fluorescent emissions are captured.
| 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 100.
| Sample_platform_id | GPL570
| Sample_contact_name | Yonghong,,Xiao
| Sample_contact_email | yonghong_xiao@yahoo.com
| Sample_contact_institute | Dana-Farber Cancer Institute
| Sample_contact_address | 450 Brookline Ave., HIM218A
| Sample_contact_city | Boston
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02115
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM231nnn/GSM231706/suppl/GSM231706.CEL.gz
| Sample_series_id | GSE9171
| Sample_series_id | GSE9200
| Sample_data_row_count | 54675
| |
|
GSM231707 | GPL570 |
|
Glioblastoma tumor GBM_355
|
human glioblastoma tumor
|
Human glioblastoma tumor
|
Gene expression data from human glioblastoma tumor.
|
Sample_geo_accession | GSM231707
| Sample_status | Public on Apr 29 2008
| Sample_submission_date | Sep 26 2007
| Sample_last_update_date | Aug 14 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| 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 15 microg total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| Sample_hyb_protocol | Following fragmentation, cRNA were hybridized for 16 hr at 45C on GeneChip Human Genome U133Plus2.0. The chips are then transferred to a fluidics instrument that performs washes to remove cRNA that has not hybridized to its complementary oligonucleotide probe. The bound cRNA is then fluorescently labeled using phycoerythrin-conjugated streptavidin (SAPE); additional fluors are then added using biotinylated anti-streptavidin antibody and additional SAPE.
| Sample_scan_protocol | Each cRNA bound at its complementary oligonucleotide is excited using a confocal laser scanner, and the positions and intensities of the fluorescent emissions are captured.
| 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 100.
| Sample_platform_id | GPL570
| Sample_contact_name | Yonghong,,Xiao
| Sample_contact_email | yonghong_xiao@yahoo.com
| Sample_contact_institute | Dana-Farber Cancer Institute
| Sample_contact_address | 450 Brookline Ave., HIM218A
| Sample_contact_city | Boston
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02115
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM231nnn/GSM231707/suppl/GSM231707.CEL.gz
| Sample_series_id | GSE9171
| Sample_series_id | GSE9200
| Sample_data_row_count | 54675
| |
|
GSM231708 | GPL570 |
|
Glioblastoma cell line GBM_Hs683
|
human glioblastoma cell line
|
Human glioblastoma cell line
|
Gene expression data from human glioblastoma cell line.
|
Sample_geo_accession | GSM231708
| Sample_status | Public on Apr 29 2008
| Sample_submission_date | Sep 26 2007
| Sample_last_update_date | Aug 14 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| 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 15 microg total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| Sample_hyb_protocol | Following fragmentation, cRNA were hybridized for 16 hr at 45C on GeneChip Human Genome U133Plus2.0. The chips are then transferred to a fluidics instrument that performs washes to remove cRNA that has not hybridized to its complementary oligonucleotide probe. The bound cRNA is then fluorescently labeled using phycoerythrin-conjugated streptavidin (SAPE); additional fluors are then added using biotinylated anti-streptavidin antibody and additional SAPE.
| Sample_scan_protocol | Each cRNA bound at its complementary oligonucleotide is excited using a confocal laser scanner, and the positions and intensities of the fluorescent emissions are captured.
| 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 100.
| Sample_platform_id | GPL570
| Sample_contact_name | Yonghong,,Xiao
| Sample_contact_email | yonghong_xiao@yahoo.com
| Sample_contact_institute | Dana-Farber Cancer Institute
| Sample_contact_address | 450 Brookline Ave., HIM218A
| Sample_contact_city | Boston
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02115
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM231nnn/GSM231708/suppl/GSM231708.CEL.gz
| Sample_series_id | GSE9171
| Sample_series_id | GSE9200
| Sample_data_row_count | 54675
| |
|
GSM231709 | GPL570 |
|
Glioblastoma cell line GBM_LN18
|
human glioblastoma cell line
|
Human glioblastoma cell line
|
Gene expression data from human glioblastoma cell line.
|
Sample_geo_accession | GSM231709
| Sample_status | Public on Apr 29 2008
| Sample_submission_date | Sep 26 2007
| Sample_last_update_date | Aug 14 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| 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 15 microg total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| Sample_hyb_protocol | Following fragmentation, cRNA were hybridized for 16 hr at 45C on GeneChip Human Genome U133Plus2.0. The chips are then transferred to a fluidics instrument that performs washes to remove cRNA that has not hybridized to its complementary oligonucleotide probe. The bound cRNA is then fluorescently labeled using phycoerythrin-conjugated streptavidin (SAPE); additional fluors are then added using biotinylated anti-streptavidin antibody and additional SAPE.
| Sample_scan_protocol | Each cRNA bound at its complementary oligonucleotide is excited using a confocal laser scanner, and the positions and intensities of the fluorescent emissions are captured.
| 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 100.
| Sample_platform_id | GPL570
| Sample_contact_name | Yonghong,,Xiao
| Sample_contact_email | yonghong_xiao@yahoo.com
| Sample_contact_institute | Dana-Farber Cancer Institute
| Sample_contact_address | 450 Brookline Ave., HIM218A
| Sample_contact_city | Boston
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02115
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM231nnn/GSM231709/suppl/GSM231709.CEL.gz
| Sample_series_id | GSE9171
| Sample_series_id | GSE9200
| Sample_data_row_count | 54675
| |
|
GSM231710 | GPL570 |
|
Glioblastoma cell line GBM_LN215
|
human glioblastoma cell line
|
Human glioblastoma cell line
|
Gene expression data from human glioblastoma cell line.
|
Sample_geo_accession | GSM231710
| Sample_status | Public on Apr 29 2008
| Sample_submission_date | Sep 26 2007
| Sample_last_update_date | Aug 14 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| 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 15 microg total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| Sample_hyb_protocol | Following fragmentation, cRNA were hybridized for 16 hr at 45C on GeneChip Human Genome U133Plus2.0. The chips are then transferred to a fluidics instrument that performs washes to remove cRNA that has not hybridized to its complementary oligonucleotide probe. The bound cRNA is then fluorescently labeled using phycoerythrin-conjugated streptavidin (SAPE); additional fluors are then added using biotinylated anti-streptavidin antibody and additional SAPE.
| Sample_scan_protocol | Each cRNA bound at its complementary oligonucleotide is excited using a confocal laser scanner, and the positions and intensities of the fluorescent emissions are captured.
| 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 100.
| Sample_platform_id | GPL570
| Sample_contact_name | Yonghong,,Xiao
| Sample_contact_email | yonghong_xiao@yahoo.com
| Sample_contact_institute | Dana-Farber Cancer Institute
| Sample_contact_address | 450 Brookline Ave., HIM218A
| Sample_contact_city | Boston
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02115
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM231nnn/GSM231710/suppl/GSM231710.CEL.gz
| Sample_series_id | GSE9171
| Sample_series_id | GSE9200
| Sample_data_row_count | 54675
| |
|
GSM231711 | GPL570 |
|
Glioblastoma cell line GBM_LN229
|
human glioblastoma cell line
|
Human glioblastoma cell line
|
Gene expression data from human glioblastoma cell line.
|
Sample_geo_accession | GSM231711
| Sample_status | Public on Apr 29 2008
| Sample_submission_date | Sep 26 2007
| Sample_last_update_date | Aug 14 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_molecule_ch1 | polyA 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 6 microg total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| Sample_hyb_protocol | Following fragmentation, 10 microg of cRNA were hybridized for 16 hr at 45C on GeneChip Drosophila Genome Array. GeneChips 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 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 100.
| Sample_platform_id | GPL570
| Sample_contact_name | Yonghong,,Xiao
| Sample_contact_email | yonghong_xiao@yahoo.com
| Sample_contact_institute | Dana-Farber Cancer Institute
| Sample_contact_address | 450 Brookline Ave., HIM218A
| Sample_contact_city | Boston
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02115
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM231nnn/GSM231711/suppl/GSM231711.CEL.gz
| Sample_series_id | GSE9171
| Sample_series_id | GSE9200
| Sample_data_row_count | 54675
| |
|
GSM231712 | GPL570 |
|
Glioblastoma cell line GBM_LN235
|
human glioblastoma cell line
|
Human glioblastoma cell line
|
Gene expression data from human glioblastoma cell line.
|
Sample_geo_accession | GSM231712
| Sample_status | Public on Apr 29 2008
| Sample_submission_date | Sep 26 2007
| Sample_last_update_date | Aug 14 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| 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 15 microg total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| Sample_hyb_protocol | Following fragmentation, cRNA were hybridized for 16 hr at 45C on GeneChip Human Genome U133Plus2.0. The chips are then transferred to a fluidics instrument that performs washes to remove cRNA that has not hybridized to its complementary oligonucleotide probe. The bound cRNA is then fluorescently labeled using phycoerythrin-conjugated streptavidin (SAPE); additional fluors are then added using biotinylated anti-streptavidin antibody and additional SAPE.
| Sample_scan_protocol | Each cRNA bound at its complementary oligonucleotide is excited using a confocal laser scanner, and the positions and intensities of the fluorescent emissions are captured.
| 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 100.
| Sample_platform_id | GPL570
| Sample_contact_name | Yonghong,,Xiao
| Sample_contact_email | yonghong_xiao@yahoo.com
| Sample_contact_institute | Dana-Farber Cancer Institute
| Sample_contact_address | 450 Brookline Ave., HIM218A
| Sample_contact_city | Boston
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02115
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM231nnn/GSM231712/suppl/GSM231712.CEL.gz
| Sample_series_id | GSE9171
| Sample_series_id | GSE9200
| Sample_data_row_count | 54675
| |
|
GSM231713 | GPL570 |
|
Glioblastoma cell line GBM_LN319
|
human glioblastoma cell line
|
Human glioblastoma cell line
|
Gene expression data from human glioblastoma cell line.
|
Sample_geo_accession | GSM231713
| Sample_status | Public on Apr 29 2008
| Sample_submission_date | Sep 26 2007
| Sample_last_update_date | Aug 14 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| 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 15 microg total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| Sample_hyb_protocol | Following fragmentation, cRNA were hybridized for 16 hr at 45C on GeneChip Human Genome U133Plus2.0. The chips are then transferred to a fluidics instrument that performs washes to remove cRNA that has not hybridized to its complementary oligonucleotide probe. The bound cRNA is then fluorescently labeled using phycoerythrin-conjugated streptavidin (SAPE); additional fluors are then added using biotinylated anti-streptavidin antibody and additional SAPE.
| Sample_scan_protocol | Each cRNA bound at its complementary oligonucleotide is excited using a confocal laser scanner, and the positions and intensities of the fluorescent emissions are captured.
| 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 100.
| Sample_platform_id | GPL570
| Sample_contact_name | Yonghong,,Xiao
| Sample_contact_email | yonghong_xiao@yahoo.com
| Sample_contact_institute | Dana-Farber Cancer Institute
| Sample_contact_address | 450 Brookline Ave., HIM218A
| Sample_contact_city | Boston
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02115
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM231nnn/GSM231713/suppl/GSM231713.CEL.gz
| Sample_series_id | GSE9171
| Sample_series_id | GSE9200
| Sample_data_row_count | 54675
| |
|
GSM231714 | GPL570 |
|
Glioblastoma cell line GBM_LN340
|
human glioblastoma cell line
|
Human glioblastoma cell line
|
Gene expression data from human glioblastoma cell line.
|
Sample_geo_accession | GSM231714
| Sample_status | Public on Apr 29 2008
| Sample_submission_date | Sep 26 2007
| Sample_last_update_date | Aug 14 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| 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 15 microg total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| Sample_hyb_protocol | Following fragmentation, cRNA were hybridized for 16 hr at 45C on GeneChip Human Genome U133Plus2.0. The chips are then transferred to a fluidics instrument that performs washes to remove cRNA that has not hybridized to its complementary oligonucleotide probe. The bound cRNA is then fluorescently labeled using phycoerythrin-conjugated streptavidin (SAPE); additional fluors are then added using biotinylated anti-streptavidin antibody and additional SAPE.
| Sample_scan_protocol | Each cRNA bound at its complementary oligonucleotide is excited using a confocal laser scanner, and the positions and intensities of the fluorescent emissions are captured.
| 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 100.
| Sample_platform_id | GPL570
| Sample_contact_name | Yonghong,,Xiao
| Sample_contact_email | yonghong_xiao@yahoo.com
| Sample_contact_institute | Dana-Farber Cancer Institute
| Sample_contact_address | 450 Brookline Ave., HIM218A
| Sample_contact_city | Boston
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02115
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM231nnn/GSM231714/suppl/GSM231714.CEL.gz
| Sample_series_id | GSE9171
| Sample_series_id | GSE9200
| Sample_data_row_count | 54675
| |
|
GSM231715 | GPL570 |
|
Glioblastoma cell line GBM_LN382
|
human glioblastoma cell line
|
Human glioblastoma cell line
|
Gene expression data from human glioblastoma cell line.
|
Sample_geo_accession | GSM231715
| Sample_status | Public on Apr 29 2008
| Sample_submission_date | Sep 26 2007
| Sample_last_update_date | Aug 14 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| 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 15 microg total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| Sample_hyb_protocol | Following fragmentation, cRNA were hybridized for 16 hr at 45C on GeneChip Human Genome U133Plus2.0. The chips are then transferred to a fluidics instrument that performs washes to remove cRNA that has not hybridized to its complementary oligonucleotide probe. The bound cRNA is then fluorescently labeled using phycoerythrin-conjugated streptavidin (SAPE); additional fluors are then added using biotinylated anti-streptavidin antibody and additional SAPE.
| Sample_scan_protocol | Each cRNA bound at its complementary oligonucleotide is excited using a confocal laser scanner, and the positions and intensities of the fluorescent emissions are captured.
| 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 100.
| Sample_platform_id | GPL570
| Sample_contact_name | Yonghong,,Xiao
| Sample_contact_email | yonghong_xiao@yahoo.com
| Sample_contact_institute | Dana-Farber Cancer Institute
| Sample_contact_address | 450 Brookline Ave., HIM218A
| Sample_contact_city | Boston
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02115
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM231nnn/GSM231715/suppl/GSM231715.CEL.gz
| Sample_series_id | GSE9171
| Sample_series_id | GSE9200
| Sample_data_row_count | 54675
| |
|
GSM231716 | GPL570 |
|
Glioblastoma cell line GBM_LN443
|
human glioblastoma cell line
|
Human glioblastoma cell line
|
Gene expression data from human glioblastoma cell line.
|
Sample_geo_accession | GSM231716
| Sample_status | Public on Apr 29 2008
| Sample_submission_date | Sep 26 2007
| Sample_last_update_date | Aug 14 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| 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 15 microg total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| Sample_hyb_protocol | Following fragmentation, cRNA were hybridized for 16 hr at 45C on GeneChip Human Genome U133Plus2.0. The chips are then transferred to a fluidics instrument that performs washes to remove cRNA that has not hybridized to its complementary oligonucleotide probe. The bound cRNA is then fluorescently labeled using phycoerythrin-conjugated streptavidin (SAPE); additional fluors are then added using biotinylated anti-streptavidin antibody and additional SAPE.
| Sample_scan_protocol | Each cRNA bound at its complementary oligonucleotide is excited using a confocal laser scanner, and the positions and intensities of the fluorescent emissions are captured.
| 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 100.
| Sample_platform_id | GPL570
| Sample_contact_name | Yonghong,,Xiao
| Sample_contact_email | yonghong_xiao@yahoo.com
| Sample_contact_institute | Dana-Farber Cancer Institute
| Sample_contact_address | 450 Brookline Ave., HIM218A
| Sample_contact_city | Boston
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02115
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM231nnn/GSM231716/suppl/GSM231716.CEL.gz
| Sample_series_id | GSE9171
| Sample_series_id | GSE9200
| Sample_data_row_count | 54675
| |
|
GSM231717 | GPL570 |
|
Glioblastoma cell line GBM_LN444
|
human glioblastoma cell line
|
Human glioblastoma cell line
|
Gene expression data from human glioblastoma cell line.
|
Sample_geo_accession | GSM231717
| Sample_status | Public on Apr 29 2008
| Sample_submission_date | Sep 26 2007
| Sample_last_update_date | Aug 14 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| 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 15 microg total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| Sample_hyb_protocol | Following fragmentation, cRNA were hybridized for 16 hr at 45C on GeneChip Human Genome U133Plus2.0. The chips are then transferred to a fluidics instrument that performs washes to remove cRNA that has not hybridized to its complementary oligonucleotide probe. The bound cRNA is then fluorescently labeled using phycoerythrin-conjugated streptavidin (SAPE); additional fluors are then added using biotinylated anti-streptavidin antibody and additional SAPE.
| Sample_scan_protocol | Each cRNA bound at its complementary oligonucleotide is excited using a confocal laser scanner, and the positions and intensities of the fluorescent emissions are captured.
| 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 100.
| Sample_platform_id | GPL570
| Sample_contact_name | Yonghong,,Xiao
| Sample_contact_email | yonghong_xiao@yahoo.com
| Sample_contact_institute | Dana-Farber Cancer Institute
| Sample_contact_address | 450 Brookline Ave., HIM218A
| Sample_contact_city | Boston
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02115
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM231nnn/GSM231717/suppl/GSM231717.CEL.gz
| Sample_series_id | GSE9171
| Sample_series_id | GSE9200
| Sample_data_row_count | 54675
| |
|
GSM231718 | GPL570 |
|
Glioblastoma cell line GBM_LN464
|
human glioblastoma cell line
|
Human glioblastoma cell line
|
Gene expression data from human glioblastoma cell line.
|
Sample_geo_accession | GSM231718
| Sample_status | Public on Apr 29 2008
| Sample_submission_date | Sep 26 2007
| Sample_last_update_date | Aug 14 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| 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 15 microg total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| Sample_hyb_protocol | Following fragmentation, cRNA were hybridized for 16 hr at 45C on GeneChip Human Genome U133Plus2.0. The chips are then transferred to a fluidics instrument that performs washes to remove cRNA that has not hybridized to its complementary oligonucleotide probe. The bound cRNA is then fluorescently labeled using phycoerythrin-conjugated streptavidin (SAPE); additional fluors are then added using biotinylated anti-streptavidin antibody and additional SAPE.
| Sample_scan_protocol | Each cRNA bound at its complementary oligonucleotide is excited using a confocal laser scanner, and the positions and intensities of the fluorescent emissions are captured.
| 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 100.
| Sample_platform_id | GPL570
| Sample_contact_name | Yonghong,,Xiao
| Sample_contact_email | yonghong_xiao@yahoo.com
| Sample_contact_institute | Dana-Farber Cancer Institute
| Sample_contact_address | 450 Brookline Ave., HIM218A
| Sample_contact_city | Boston
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02115
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM231nnn/GSM231718/suppl/GSM231718.CEL.gz
| Sample_series_id | GSE9171
| Sample_series_id | GSE9200
| Sample_data_row_count | 54675
| |
|
GSM231719 | GPL570 |
|
Glioblastoma cell line GBM_LNZ308
|
human glioblastoma cell line
|
Human glioblastoma cell line
|
Gene expression data from human glioblastoma cell line.
|
Sample_geo_accession | GSM231719
| Sample_status | Public on Apr 29 2008
| Sample_submission_date | Sep 26 2007
| Sample_last_update_date | Aug 14 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| 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 15 microg total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| Sample_hyb_protocol | Following fragmentation, cRNA were hybridized for 16 hr at 45C on GeneChip Human Genome U133Plus2.0. The chips are then transferred to a fluidics instrument that performs washes to remove cRNA that has not hybridized to its complementary oligonucleotide probe. The bound cRNA is then fluorescently labeled using phycoerythrin-conjugated streptavidin (SAPE); additional fluors are then added using biotinylated anti-streptavidin antibody and additional SAPE.
| Sample_scan_protocol | Each cRNA bound at its complementary oligonucleotide is excited using a confocal laser scanner, and the positions and intensities of the fluorescent emissions are captured.
| 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 100.
| Sample_platform_id | GPL570
| Sample_contact_name | Yonghong,,Xiao
| Sample_contact_email | yonghong_xiao@yahoo.com
| Sample_contact_institute | Dana-Farber Cancer Institute
| Sample_contact_address | 450 Brookline Ave., HIM218A
| Sample_contact_city | Boston
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02115
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM231nnn/GSM231719/suppl/GSM231719.CEL.gz
| Sample_series_id | GSE9171
| Sample_series_id | GSE9200
| Sample_data_row_count | 54675
| |
|
GSM231720 | GPL570 |
|
Glioblastoma cell line GBM_SF763
|
human glioblastoma cell line
|
Human glioblastoma cell line
|
Gene expression data from human glioblastoma cell line.
|
Sample_geo_accession | GSM231720
| Sample_status | Public on Apr 29 2008
| Sample_submission_date | Sep 26 2007
| Sample_last_update_date | Aug 14 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| 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 15 microg total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| Sample_hyb_protocol | Following fragmentation, cRNA were hybridized for 16 hr at 45C on GeneChip Human Genome U133Plus2.0. The chips are then transferred to a fluidics instrument that performs washes to remove cRNA that has not hybridized to its complementary oligonucleotide probe. The bound cRNA is then fluorescently labeled using phycoerythrin-conjugated streptavidin (SAPE); additional fluors are then added using biotinylated anti-streptavidin antibody and additional SAPE.
| Sample_scan_protocol | Each cRNA bound at its complementary oligonucleotide is excited using a confocal laser scanner, and the positions and intensities of the fluorescent emissions are captured.
| 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 100.
| Sample_platform_id | GPL570
| Sample_contact_name | Yonghong,,Xiao
| Sample_contact_email | yonghong_xiao@yahoo.com
| Sample_contact_institute | Dana-Farber Cancer Institute
| Sample_contact_address | 450 Brookline Ave., HIM218A
| Sample_contact_city | Boston
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02115
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM231nnn/GSM231720/suppl/GSM231720.CEL.gz
| Sample_series_id | GSE9171
| Sample_series_id | GSE9200
| Sample_data_row_count | 54675
| |
|
GSM231721 | GPL570 |
|
Glioblastoma cell line GBM_SF767
|
human glioblastoma cell line
|
Human glioblastoma cell line
|
Gene expression data from human glioblastoma cell line.
|
Sample_geo_accession | GSM231721
| Sample_status | Public on Apr 29 2008
| Sample_submission_date | Sep 26 2007
| Sample_last_update_date | Aug 14 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| 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 15 microg total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| Sample_hyb_protocol | Following fragmentation, cRNA were hybridized for 16 hr at 45C on GeneChip Human Genome U133Plus2.0. The chips are then transferred to a fluidics instrument that performs washes to remove cRNA that has not hybridized to its complementary oligonucleotide probe. The bound cRNA is then fluorescently labeled using phycoerythrin-conjugated streptavidin (SAPE); additional fluors are then added using biotinylated anti-streptavidin antibody and additional SAPE.
| Sample_scan_protocol | Each cRNA bound at its complementary oligonucleotide is excited using a confocal laser scanner, and the positions and intensities of the fluorescent emissions are captured.
| 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 100.
| Sample_platform_id | GPL570
| Sample_contact_name | Yonghong,,Xiao
| Sample_contact_email | yonghong_xiao@yahoo.com
| Sample_contact_institute | Dana-Farber Cancer Institute
| Sample_contact_address | 450 Brookline Ave., HIM218A
| Sample_contact_city | Boston
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02115
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM231nnn/GSM231721/suppl/GSM231721.CEL.gz
| Sample_series_id | GSE9171
| Sample_series_id | GSE9200
| Sample_data_row_count | 54675
| |
|
GSM231722 | GPL570 |
|
Glioblastoma cell line GBM_U343
|
human glioblastoma cell line
|
Human glioblastoma cell line
|
Gene expression data from human glioblastoma cell line.
|
Sample_geo_accession | GSM231722
| Sample_status | Public on Apr 29 2008
| Sample_submission_date | Sep 26 2007
| Sample_last_update_date | Aug 14 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| 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 15 microg total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| Sample_hyb_protocol | Following fragmentation, cRNA were hybridized for 16 hr at 45C on GeneChip Human Genome U133Plus2.0. The chips are then transferred to a fluidics instrument that performs washes to remove cRNA that has not hybridized to its complementary oligonucleotide probe. The bound cRNA is then fluorescently labeled using phycoerythrin-conjugated streptavidin (SAPE); additional fluors are then added using biotinylated anti-streptavidin antibody and additional SAPE.
| Sample_scan_protocol | Each cRNA bound at its complementary oligonucleotide is excited using a confocal laser scanner, and the positions and intensities of the fluorescent emissions are captured.
| 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 100.
| Sample_platform_id | GPL570
| Sample_contact_name | Yonghong,,Xiao
| Sample_contact_email | yonghong_xiao@yahoo.com
| Sample_contact_institute | Dana-Farber Cancer Institute
| Sample_contact_address | 450 Brookline Ave., HIM218A
| Sample_contact_city | Boston
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02115
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM231nnn/GSM231722/suppl/GSM231722.CEL.gz
| Sample_series_id | GSE9171
| Sample_series_id | GSE9200
| Sample_data_row_count | 54675
| |
|
GSM231723 | GPL570 |
|
Glioblastoma cell line GBM_U373
|
human glioblastoma cell line
|
Human glioblastoma cell line
|
Gene expression data from human glioblastoma cell line.
|
Sample_geo_accession | GSM231723
| Sample_status | Public on Apr 29 2008
| Sample_submission_date | Sep 26 2007
| Sample_last_update_date | Aug 14 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| 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 15 microg total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| Sample_hyb_protocol | Following fragmentation, cRNA were hybridized for 16 hr at 45C on GeneChip Human Genome U133Plus2.0. The chips are then transferred to a fluidics instrument that performs washes to remove cRNA that has not hybridized to its complementary oligonucleotide probe. The bound cRNA is then fluorescently labeled using phycoerythrin-conjugated streptavidin (SAPE); additional fluors are then added using biotinylated anti-streptavidin antibody and additional SAPE.
| Sample_scan_protocol | Each cRNA bound at its complementary oligonucleotide is excited using a confocal laser scanner, and the positions and intensities of the fluorescent emissions are captured.
| 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 100.
| Sample_platform_id | GPL570
| Sample_contact_name | Yonghong,,Xiao
| Sample_contact_email | yonghong_xiao@yahoo.com
| Sample_contact_institute | Dana-Farber Cancer Institute
| Sample_contact_address | 450 Brookline Ave., HIM218A
| Sample_contact_city | Boston
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02115
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM231nnn/GSM231723/suppl/GSM231723.CEL.gz
| Sample_series_id | GSE9171
| Sample_series_id | GSE9200
| Sample_data_row_count | 54675
| |
|
GSM231724 | GPL570 |
|
Glioblastoma cell line GBM_U87
|
human glioblastoma cell line
|
Human glioblastoma cell line
|
Gene expression data from human glioblastoma cell line.
|
Sample_geo_accession | GSM231724
| Sample_status | Public on Apr 29 2008
| Sample_submission_date | Sep 26 2007
| Sample_last_update_date | Aug 14 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| 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 15 microg total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| Sample_hyb_protocol | Following fragmentation, cRNA were hybridized for 16 hr at 45C on GeneChip Human Genome U133Plus2.0. The chips are then transferred to a fluidics instrument that performs washes to remove cRNA that has not hybridized to its complementary oligonucleotide probe. The bound cRNA is then fluorescently labeled using phycoerythrin-conjugated streptavidin (SAPE); additional fluors are then added using biotinylated anti-streptavidin antibody and additional SAPE.
| Sample_scan_protocol | Each cRNA bound at its complementary oligonucleotide is excited using a confocal laser scanner, and the positions and intensities of the fluorescent emissions are captured.
| 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 100.
| Sample_platform_id | GPL570
| Sample_contact_name | Yonghong,,Xiao
| Sample_contact_email | yonghong_xiao@yahoo.com
| Sample_contact_institute | Dana-Farber Cancer Institute
| Sample_contact_address | 450 Brookline Ave., HIM218A
| Sample_contact_city | Boston
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02115
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM231nnn/GSM231724/suppl/GSM231724.CEL.gz
| Sample_series_id | GSE9171
| Sample_series_id | GSE9200
| Sample_data_row_count | 54675
| |
|
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Make groups for comparisons |
(2 groups will be compared at a time) |
|
Select GSMs and click on "Add groups" |
Enter the group name here: |
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