Search results for the GEO ID: GSE6728 |
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|
GSM ID | GPL ID |
Select for analysis |
Title |
Source name |
Description |
Characteristics |
GSM155069 | GPL570 |
|
Granta-519 cell line mock treated
|
GRANTA-519 cell line mock treated
|
Mantle Cell Lymphoma cell line
|
Gene expression data from GRANTA cell line mock treated
|
Sample_geo_accession | GSM155069
| Sample_status | Public on Dec 31 2007
| Sample_submission_date | Jan 12 2007
| Sample_last_update_date | Dec 31 2007
| 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 followed by a cleanup using the QUIAGEN RNAesy Mini kit
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotynilated cRNA were prepared according to the standard Affymetrix protocol from 2 micrograms Total RNA (Expression Analysis Technical Manual (Affymetrix Inc)
| Sample_hyb_protocol | Following fragmentation, 10 micrograms of cRNA were hybridized for 16 hours at 45ºC on human 133 Plus 2.0 . GeneChips were washed and stained in the Affymetrix Fluidics Station 450
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix 3000 Scanner system
| Sample_data_processing | The data were analyzed with GCOS 1.4 using the Affymetrix default analysis settings and global scailing as normalization method. The target intensity used was arbitrarily set to 150
| Sample_platform_id | GPL570
| Sample_contact_name | Pedro,,Jares
| Sample_contact_email | pjares@clinic.ub.es
| Sample_contact_department | Genomics Unit
| Sample_contact_institute | IDIBAPS
| Sample_contact_address | c/ Villarroel 170
| Sample_contact_city | Barcelona
| Sample_contact_state | Barcelona
| Sample_contact_zip/postal_code | 08036
| Sample_contact_country | Spain
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM155nnn/GSM155069/suppl/GSM155069.CEL.gz
| Sample_series_id | GSE6728
| Sample_data_row_count | 54675
| |
|
GSM155070 | GPL570 |
|
Granta-519 cell line treated with emetine
|
GRANTA-519 cell line treated with emetine
|
Mantle Cell Lymphoma cell line
|
Gene expression data from GRANTA cell line treated with emetine
|
Sample_geo_accession | GSM155070
| Sample_status | Public on Dec 31 2007
| Sample_submission_date | Jan 12 2007
| Sample_last_update_date | Dec 31 2007
| 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 followed by a cleanup using the QUIAGEN RNAesy Mini kit
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotynilated cRNA were prepared according to the standard Affymetrix protocol from 2 micrograms Total RNA (Expression Analysis Technical Manual (Affymetrix Inc)
| Sample_hyb_protocol | Following fragmentation, 10 micrograms of cRNA were hybridized for 16 hours at 45ºC on human 133 Plus 2.0 . GeneChips were washed and stained in the Affymetrix Fluidics Station 450
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix 3000 Scanner system
| Sample_data_processing | The data were analyzed with GCOS 1.4 using the Affymetrix default analysis settings and global scailing as normalization method. The target intensity used was arbitrarily set to 150
| Sample_platform_id | GPL570
| Sample_contact_name | Pedro,,Jares
| Sample_contact_email | pjares@clinic.ub.es
| Sample_contact_department | Genomics Unit
| Sample_contact_institute | IDIBAPS
| Sample_contact_address | c/ Villarroel 170
| Sample_contact_city | Barcelona
| Sample_contact_state | Barcelona
| Sample_contact_zip/postal_code | 08036
| Sample_contact_country | Spain
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM155nnn/GSM155070/suppl/GSM155070.CEL.gz
| Sample_series_id | GSE6728
| Sample_data_row_count | 54675
| |
|
GSM155071 | GPL570 |
|
Granta- 519 cell line treated with emetine followed by actinomycin D treatment. Pool of a time course
|
Granta-519 cell line treated with emetine followed by actinomycin D treatment. Pool of a time course
|
Mantle Cell Lymphoma cell line
|
Gene expression data from GRANTA cell line treated with emetine
|
Sample_geo_accession | GSM155071
| Sample_status | Public on Dec 31 2007
| Sample_submission_date | Jan 12 2007
| Sample_last_update_date | Dec 31 2007
| 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 followed by a cleanup using the QUIAGEN RNAesy Mini kit
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotynilated cRNA were prepared according to the standard Affymetrix protocol from 2 micrograms Total RNA (Expression Analysis Technical Manual (Affymetrix Inc)
| Sample_hyb_protocol | Following fragmentation, 10 micrograms of cRNA were hybridized for 16 hours at 45ºC on human 133 Plus 2.0 . GeneChips were washed and stained in the Affymetrix Fluidics Station 450
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix 3000 Scanner system
| Sample_data_processing | The data were analyzed with GCOS 1.4 using the Affymetrix default analysis settings and global scailing as normalization method. The target intensity used was arbitrarily set to 150
| Sample_platform_id | GPL570
| Sample_contact_name | Pedro,,Jares
| Sample_contact_email | pjares@clinic.ub.es
| Sample_contact_department | Genomics Unit
| Sample_contact_institute | IDIBAPS
| Sample_contact_address | c/ Villarroel 170
| Sample_contact_city | Barcelona
| Sample_contact_state | Barcelona
| Sample_contact_zip/postal_code | 08036
| Sample_contact_country | Spain
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM155nnn/GSM155071/suppl/GSM155071.CEL.gz
| Sample_series_id | GSE6728
| Sample_data_row_count | 54675
| |
|
GSM155072 | GPL570 |
|
REC-1cell line mock treated
|
REC-1 cell line mock treated
|
Mantle Cell Lymphoma cell line
|
Gene expression data from REC-1 cell line mock treated
|
Sample_geo_accession | GSM155072
| Sample_status | Public on Dec 31 2007
| Sample_submission_date | Jan 12 2007
| Sample_last_update_date | Dec 31 2007
| 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 followed by a cleanup using the QUIAGEN RNAesy Mini kit
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotynilated cRNA were prepared according to the standard Affymetrix protocol from 2 micrograms Total RNA (Expression Analysis Technical Manual (Affymetrix Inc)
| Sample_hyb_protocol | Following fragmentation, 10 micrograms of cRNA were hybridized for 16 hours at 45ºC on human 133 Plus 2.0 . GeneChips were washed and stained in the Affymetrix Fluidics Station 450
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix 3000 Scanner system
| Sample_data_processing | The data were analyzed with GCOS 1.4 using the Affymetrix default analysis settings and global scailing as normalization method. The target intensity used was arbitrarily set to 150
| Sample_platform_id | GPL570
| Sample_contact_name | Pedro,,Jares
| Sample_contact_email | pjares@clinic.ub.es
| Sample_contact_department | Genomics Unit
| Sample_contact_institute | IDIBAPS
| Sample_contact_address | c/ Villarroel 170
| Sample_contact_city | Barcelona
| Sample_contact_state | Barcelona
| Sample_contact_zip/postal_code | 08036
| Sample_contact_country | Spain
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM155nnn/GSM155072/suppl/GSM155072.CEL.gz
| Sample_series_id | GSE6728
| Sample_data_row_count | 54675
| |
|
GSM155073 | GPL570 |
|
REC-1cell line treated with emetine
|
REC-1 cell line treated with emetine
|
Mantle Cell Lymphoma cell line
|
Gene expression data from GRANTA cell line treated with emetine
|
Sample_geo_accession | GSM155073
| Sample_status | Public on Dec 31 2007
| Sample_submission_date | Jan 12 2007
| Sample_last_update_date | Dec 31 2007
| 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 followed by a cleanup using the QUIAGEN RNAesy Mini kit
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotynilated cRNA were prepared according to the standard Affymetrix protocol from 2 micrograms Total RNA (Expression Analysis Technical Manual (Affymetrix Inc)
| Sample_hyb_protocol | Following fragmentation, 10 micrograms of cRNA were hybridized for 16 hours at 45ºC on human 133 Plus 2.0 . GeneChips were washed and stained in the Affymetrix Fluidics Station 450
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix 3000 Scanner system
| Sample_data_processing | The data were analyzed with GCOS 1.4 using the Affymetrix default analysis settings and global scailing as normalization method. The target intensity used was arbitrarily set to 150
| Sample_platform_id | GPL570
| Sample_contact_name | Pedro,,Jares
| Sample_contact_email | pjares@clinic.ub.es
| Sample_contact_department | Genomics Unit
| Sample_contact_institute | IDIBAPS
| Sample_contact_address | c/ Villarroel 170
| Sample_contact_city | Barcelona
| Sample_contact_state | Barcelona
| Sample_contact_zip/postal_code | 08036
| Sample_contact_country | Spain
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM155nnn/GSM155073/suppl/GSM155073.CEL.gz
| Sample_series_id | GSE6728
| Sample_data_row_count | 54675
| |
|
GSM155074 | GPL570 |
|
REC-1cell line treated with emetine followed by actinomycin D treatment. Pool of a time course
|
REC-1 cell line treated with emetine followed by actinomycin D treatment. Pool of a time course
|
Mantle Cell Lymphoma cell line
|
Gene expression data from Rec-1 cell line treated with emetine
|
Sample_geo_accession | GSM155074
| Sample_status | Public on Dec 31 2007
| Sample_submission_date | Jan 12 2007
| Sample_last_update_date | Dec 31 2007
| 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 followed by a cleanup using the QUIAGEN RNAesy Mini kit
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotynilated cRNA were prepared according to the standard Affymetrix protocol from 2 micrograms Total RNA (Expression Analysis Technical Manual (Affymetrix Inc)
| Sample_hyb_protocol | Following fragmentation, 10 micrograms of cRNA were hybridized for 16 hours at 45ºC on human 133 Plus 2.0 . GeneChips were washed and stained in the Affymetrix Fluidics Station 450
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix 3000 Scanner system
| Sample_data_processing | The data were analyzed with GCOS 1.4 using the Affymetrix default analysis settings and global scailing as normalization method. The target intensity used was arbitrarily set to 150
| Sample_platform_id | GPL570
| Sample_contact_name | Pedro,,Jares
| Sample_contact_email | pjares@clinic.ub.es
| Sample_contact_department | Genomics Unit
| Sample_contact_institute | IDIBAPS
| Sample_contact_address | c/ Villarroel 170
| Sample_contact_city | Barcelona
| Sample_contact_state | Barcelona
| Sample_contact_zip/postal_code | 08036
| Sample_contact_country | Spain
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM155nnn/GSM155074/suppl/GSM155074.CEL.gz
| Sample_series_id | GSE6728
| Sample_data_row_count | 54675
| |
|
GSM155075 | GPL570 |
|
UPN-1cell line mock treated
|
UPN-1 cell line mock treated
|
Mantle Cell Lymphoma cell line
|
Gene expression data from UPN-1 cell line mock treated
|
Sample_geo_accession | GSM155075
| Sample_status | Public on Dec 31 2007
| Sample_submission_date | Jan 12 2007
| Sample_last_update_date | Dec 31 2007
| 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 followed by a cleanup using the QUIAGEN RNAesy Mini kit
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotynilated cRNA were prepared according to the standard Affymetrix protocol from 2 micrograms Total RNA (Expression Analysis Technical Manual (Affymetrix Inc)
| Sample_hyb_protocol | Following fragmentation, 10 micrograms of cRNA were hybridized for 16 hours at 45ºC on human 133 Plus 2.0 . GeneChips were washed and stained in the Affymetrix Fluidics Station 450
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix 3000 Scanner system
| Sample_data_processing | The data were analyzed with GCOS 1.4 using the Affymetrix default analysis settings and global scailing as normalization method. The target intensity used was arbitrarily set to 150
| Sample_platform_id | GPL570
| Sample_contact_name | Pedro,,Jares
| Sample_contact_email | pjares@clinic.ub.es
| Sample_contact_department | Genomics Unit
| Sample_contact_institute | IDIBAPS
| Sample_contact_address | c/ Villarroel 170
| Sample_contact_city | Barcelona
| Sample_contact_state | Barcelona
| Sample_contact_zip/postal_code | 08036
| Sample_contact_country | Spain
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM155nnn/GSM155075/suppl/GSM155075.CEL.gz
| Sample_series_id | GSE6728
| Sample_data_row_count | 54675
| |
|
GSM155076 | GPL570 |
|
UPN-1cell line treated with emetine
|
UPN-1 cell line treated with emetine
|
Mantle Cell Lymphoma cell line
|
Gene expression data from UPN-1 cell line treated with emetine
|
Sample_geo_accession | GSM155076
| Sample_status | Public on Dec 31 2007
| Sample_submission_date | Jan 12 2007
| Sample_last_update_date | Dec 31 2007
| 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 followed by a cleanup using the QUIAGEN RNAesy Mini kit
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotynilated cRNA were prepared according to the standard Affymetrix protocol from 2 micrograms Total RNA (Expression Analysis Technical Manual (Affymetrix Inc)
| Sample_hyb_protocol | Following fragmentation, 10 micrograms of cRNA were hybridized for 16 hours at 45ºC on human 133 Plus 2.0 . GeneChips were washed and stained in the Affymetrix Fluidics Station 450
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix 3000 Scanner system
| Sample_data_processing | The data were analyzed with GCOS 1.4 using the Affymetrix default analysis settings and global scailing as normalization method. The target intensity used was arbitrarily set to 150
| Sample_platform_id | GPL570
| Sample_contact_name | Pedro,,Jares
| Sample_contact_email | pjares@clinic.ub.es
| Sample_contact_department | Genomics Unit
| Sample_contact_institute | IDIBAPS
| Sample_contact_address | c/ Villarroel 170
| Sample_contact_city | Barcelona
| Sample_contact_state | Barcelona
| Sample_contact_zip/postal_code | 08036
| Sample_contact_country | Spain
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM155nnn/GSM155076/suppl/GSM155076.CEL.gz
| Sample_series_id | GSE6728
| Sample_data_row_count | 54675
| |
|
GSM155077 | GPL570 |
|
UPN-1cell line treated with emetine followed by actinomycin D treatment. Pool of a time course
|
UPN-1 cell line treated with emetine followed by actinomycin D treatment. Pool of a time course
|
Mantle Cell Lymphoma cell line
|
Gene expression data from UPN-1 cell line treated with emetine
|
Sample_geo_accession | GSM155077
| Sample_status | Public on Dec 31 2007
| Sample_submission_date | Jan 12 2007
| Sample_last_update_date | Dec 31 2007
| 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 followed by a cleanup using the QUIAGEN RNAesy Mini kit
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotynilated cRNA were prepared according to the standard Affymetrix protocol from 2 micrograms Total RNA (Expression Analysis Technical Manual (Affymetrix Inc)
| Sample_hyb_protocol | Following fragmentation, 10 micrograms of cRNA were hybridized for 16 hours at 45ºC on human 133 Plus 2.0 . GeneChips were washed and stained in the Affymetrix Fluidics Station 450
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix 3000 Scanner system
| Sample_data_processing | The data were analyzed with GCOS 1.4 using the Affymetrix default analysis settings and global scailing as normalization method. The target intensity used was arbitrarily set to 150
| Sample_platform_id | GPL570
| Sample_contact_name | Pedro,,Jares
| Sample_contact_email | pjares@clinic.ub.es
| Sample_contact_department | Genomics Unit
| Sample_contact_institute | IDIBAPS
| Sample_contact_address | c/ Villarroel 170
| Sample_contact_city | Barcelona
| Sample_contact_state | Barcelona
| Sample_contact_zip/postal_code | 08036
| Sample_contact_country | Spain
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM155nnn/GSM155077/suppl/GSM155077.CEL.gz
| Sample_series_id | GSE6728
| Sample_data_row_count | 54675
| |
|
GSM155078 | GPL570 |
|
HBL-2 cell line mock treated
|
HBL-2 cell line mock treated
|
Mantle Cell Lymphoma cell line
|
Gene expression data from HBL-2 cell line mock treated
|
Sample_geo_accession | GSM155078
| Sample_status | Public on Dec 31 2007
| Sample_submission_date | Jan 12 2007
| Sample_last_update_date | Dec 31 2007
| 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 followed by a cleanup using the QUIAGEN RNAesy Mini kit
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotynilated cRNA were prepared according to the standard Affymetrix protocol from 2 micrograms Total RNA (Expression Analysis Technical Manual (Affymetrix Inc)
| Sample_hyb_protocol | Following fragmentation, 10 micrograms of cRNA were hybridized for 16 hours at 45ºC on human 133 Plus 2.0 . GeneChips were washed and stained in the Affymetrix Fluidics Station 450
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix 3000 Scanner system
| Sample_data_processing | The data were analyzed with GCOS 1.4 using the Affymetrix default analysis settings and global scailing as normalization method. The target intensity used was arbitrarily set to 150
| Sample_platform_id | GPL570
| Sample_contact_name | Pedro,,Jares
| Sample_contact_email | pjares@clinic.ub.es
| Sample_contact_department | Genomics Unit
| Sample_contact_institute | IDIBAPS
| Sample_contact_address | c/ Villarroel 170
| Sample_contact_city | Barcelona
| Sample_contact_state | Barcelona
| Sample_contact_zip/postal_code | 08036
| Sample_contact_country | Spain
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM155nnn/GSM155078/suppl/GSM155078.CEL.gz
| Sample_series_id | GSE6728
| Sample_data_row_count | 54675
| |
|
GSM155079 | GPL570 |
|
HBL-2 cell line treated with emetine
|
HBL-2 cell line treated with emetine
|
Mantle Cell Lymphoma cell line
|
Gene expression data from HBL-2 cell line treated with emetine
|
Sample_geo_accession | GSM155079
| Sample_status | Public on Dec 31 2007
| Sample_submission_date | Jan 12 2007
| Sample_last_update_date | Dec 31 2007
| 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 followed by a cleanup using the QUIAGEN RNAesy Mini kit
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotynilated cRNA were prepared according to the standard Affymetrix protocol from 2 micrograms Total RNA (Expression Analysis Technical Manual (Affymetrix Inc)
| Sample_hyb_protocol | Following fragmentation, 10 micrograms of cRNA were hybridized for 16 hours at 45ºC on human 133 Plus 2.0 . GeneChips were washed and stained in the Affymetrix Fluidics Station 450
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix 3000 Scanner system
| Sample_data_processing | The data were analyzed with GCOS 1.4 using the Affymetrix default analysis settings and global scailing as normalization method. The target intensity used was arbitrarily set to 150
| Sample_platform_id | GPL570
| Sample_contact_name | Pedro,,Jares
| Sample_contact_email | pjares@clinic.ub.es
| Sample_contact_department | Genomics Unit
| Sample_contact_institute | IDIBAPS
| Sample_contact_address | c/ Villarroel 170
| Sample_contact_city | Barcelona
| Sample_contact_state | Barcelona
| Sample_contact_zip/postal_code | 08036
| Sample_contact_country | Spain
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM155nnn/GSM155079/suppl/GSM155079.CEL.gz
| Sample_series_id | GSE6728
| Sample_data_row_count | 54675
| |
|
GSM155080 | GPL570 |
|
HBL-2 cell line treated with emetine followed by actinomycin D treatment. Pool of a time course
|
HBL-2 cell line treated with emetine followed by actinomycin D treatment. Pool of a time course
|
Mantle Cell Lymphoma cell line
|
Gene expression data from HBL-2 cell line treated with emetine
|
Sample_geo_accession | GSM155080
| Sample_status | Public on Dec 31 2007
| Sample_submission_date | Jan 12 2007
| Sample_last_update_date | Dec 31 2007
| 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 followed by a cleanup using the QUIAGEN RNAesy Mini kit
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotynilated cRNA were prepared according to the standard Affymetrix protocol from 2 micrograms Total RNA (Expression Analysis Technical Manual (Affymetrix Inc)
| Sample_hyb_protocol | Following fragmentation, 10 micrograms of cRNA were hybridized for 16 hours at 45ºC on human 133 Plus 2.0 . GeneChips were washed and stained in the Affymetrix Fluidics Station 450
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix 3000 Scanner system
| Sample_data_processing | The data were analyzed with GCOS 1.4 using the Affymetrix default analysis settings and global scailing as normalization method. The target intensity used was arbitrarily set to 150
| Sample_platform_id | GPL570
| Sample_contact_name | Pedro,,Jares
| Sample_contact_email | pjares@clinic.ub.es
| Sample_contact_department | Genomics Unit
| Sample_contact_institute | IDIBAPS
| Sample_contact_address | c/ Villarroel 170
| Sample_contact_city | Barcelona
| Sample_contact_state | Barcelona
| Sample_contact_zip/postal_code | 08036
| Sample_contact_country | Spain
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM155nnn/GSM155080/suppl/GSM155080.CEL.gz
| Sample_series_id | GSE6728
| Sample_data_row_count | 54675
| |
|
GSM155081 | GPL570 |
|
JEKO-1 cell line mock treated
|
JEKO-1 cell line mock treated
|
Mantle Cell Lymphoma cell line
|
Gene expression data from JEKO-1 cell line mock treated
|
Sample_geo_accession | GSM155081
| Sample_status | Public on Dec 31 2007
| Sample_submission_date | Jan 12 2007
| Sample_last_update_date | Dec 31 2007
| 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 followed by a cleanup using the QUIAGEN RNAesy Mini kit
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotynilated cRNA were prepared according to the standard Affymetrix protocol from 2 micrograms Total RNA (Expression Analysis Technical Manual (Affymetrix Inc)
| Sample_hyb_protocol | Following fragmentation, 10 micrograms of cRNA were hybridized for 16 hours at 45ºC on human 133 Plus 2.0 . GeneChips were washed and stained in the Affymetrix Fluidics Station 450
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix 3000 Scanner system
| Sample_data_processing | The data were analyzed with GCOS 1.4 using the Affymetrix default analysis settings and global scailing as normalization method. The target intensity used was arbitrarily set to 150
| Sample_platform_id | GPL570
| Sample_contact_name | Pedro,,Jares
| Sample_contact_email | pjares@clinic.ub.es
| Sample_contact_department | Genomics Unit
| Sample_contact_institute | IDIBAPS
| Sample_contact_address | c/ Villarroel 170
| Sample_contact_city | Barcelona
| Sample_contact_state | Barcelona
| Sample_contact_zip/postal_code | 08036
| Sample_contact_country | Spain
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM155nnn/GSM155081/suppl/GSM155081.CEL.gz
| Sample_series_id | GSE6728
| Sample_data_row_count | 54675
| |
|
GSM155082 | GPL570 |
|
JEKO-1 cell line treated with emetine
|
JEKO-1 cell line treated with emetine
|
Mantle Cell Lymphoma cell line
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Gene expression data from JEKO-1 cell line treated with emetine
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Sample_geo_accession | GSM155082
| Sample_status | Public on Dec 31 2007
| Sample_submission_date | Jan 12 2007
| Sample_last_update_date | Dec 31 2007
| 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 followed by a cleanup using the QUIAGEN RNAesy Mini kit
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotynilated cRNA were prepared according to the standard Affymetrix protocol from 2 micrograms Total RNA (Expression Analysis Technical Manual (Affymetrix Inc)
| Sample_hyb_protocol | Following fragmentation, 10 micrograms of cRNA were hybridized for 16 hours at 45ºC on human 133 Plus 2.0 . GeneChips were washed and stained in the Affymetrix Fluidics Station 450
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix 3000 Scanner system
| Sample_data_processing | The data were analyzed with GCOS 1.4 using the Affymetrix default analysis settings and global scailing as normalization method. The target intensity used was arbitrarily set to 150
| Sample_platform_id | GPL570
| Sample_contact_name | Pedro,,Jares
| Sample_contact_email | pjares@clinic.ub.es
| Sample_contact_department | Genomics Unit
| Sample_contact_institute | IDIBAPS
| Sample_contact_address | c/ Villarroel 170
| Sample_contact_city | Barcelona
| Sample_contact_state | Barcelona
| Sample_contact_zip/postal_code | 08036
| Sample_contact_country | Spain
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM155nnn/GSM155082/suppl/GSM155082.CEL.gz
| Sample_series_id | GSE6728
| Sample_data_row_count | 54675
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GSM155083 | GPL570 |
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JEKO-1 cell line treated with emetine followed by actinomycin D treatment. Pool of a time course
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JEKO-1 cell line treated with emetine followed by actinomycin D treatment. Pool of a time course
|
Mantle Cell Lymphoma cell line
|
Gene expression data from JEKO-1 cell line treated with emetine
|
Sample_geo_accession | GSM155083
| Sample_status | Public on Dec 31 2007
| Sample_submission_date | Jan 12 2007
| Sample_last_update_date | Dec 31 2007
| 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 followed by a cleanup using the QUIAGEN RNAesy Mini kit
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotynilated cRNA were prepared according to the standard Affymetrix protocol from 2 micrograms Total RNA (Expression Analysis Technical Manual (Affymetrix Inc)
| Sample_hyb_protocol | Following fragmentation, 10 micrograms of cRNA were hybridized for 16 hours at 45ºC on human 133 Plus 2.0 . GeneChips were washed and stained in the Affymetrix Fluidics Station 450
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix 3000 Scanner system
| Sample_data_processing | The data were analyzed with GCOS 1.4 using the Affymetrix default analysis settings and global scailing as normalization method. The target intensity used was arbitrarily set to 150
| Sample_platform_id | GPL570
| Sample_contact_name | Pedro,,Jares
| Sample_contact_email | pjares@clinic.ub.es
| Sample_contact_department | Genomics Unit
| Sample_contact_institute | IDIBAPS
| Sample_contact_address | c/ Villarroel 170
| Sample_contact_city | Barcelona
| Sample_contact_state | Barcelona
| Sample_contact_zip/postal_code | 08036
| Sample_contact_country | Spain
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM155nnn/GSM155083/suppl/GSM155083.CEL.gz
| Sample_series_id | GSE6728
| Sample_data_row_count | 54675
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