Search results for the GEO ID: GSE28019 |
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|
GSM ID | GPL ID |
Select for analysis |
Title |
Source name |
Description |
Characteristics |
GSM692854 | GPL570 |
|
sknfi
|
sknfi
|
cell type: Neuroblastoma cell
cell line: sknfi
|
|
Sample_geo_accession | GSM692854
| Sample_status | Public on Mar 16 2013
| Sample_submission_date | Mar 17 2011
| Sample_last_update_date | Mar 16 2013
| 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 | Total RNA was isolated using Trizol (Invitrogen) and purified with RNeasy (Qiagen) according to manufacturer’s protocol
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | RNA sample integrity was checked on an Agilent 2100 Bioanalyzer (Agilent Technologies). 4 µg of total RNA was used for cRNA synthesis and fragmented. Labeling was performed with One-Cycle cDNA synthesis Kit (Affymetrix) according to manufacturer’s protocol. Sample quality was checked on a Bioanalyzer prior and after fragmentation.
| Sample_hyb_protocol | 10 µg of labeled cRNA was hybridized to Affymetrix Human genome U133 Plus 2.0 arrays according to manufacturer’s protocol (Affymetrix).
| Sample_scan_protocol | Arrays were scanned with a GeneChip Scanner 3000 (Affymetrix) according to manufacturer’s protocol
| Sample_data_processing = Expression data (cel files) were normalized with the MAS5.0 algorithm (target signal | 100) using GCOS software (Affymetrix)
| Sample_platform_id | GPL570
| Sample_contact_name | Rogier,,Versteeg
| Sample_contact_email | r.versteeg@amc.uva.nl
| Sample_contact_department | Department of Human Genetics
| Sample_contact_institute | Academic Medical Centre, University of Amsterdam
| Sample_contact_address | P.O. Box 22700
| Sample_contact_city | Amsterdam
| Sample_contact_zip/postal_code | 1100DE
| Sample_contact_country | Netherlands
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM692nnn/GSM692854/suppl/GSM692854.CEL.gz
| Sample_series_id | GSE28019
| Sample_data_row_count | 54675
| |
|
GSM692855 | GPL570 |
|
sknas
|
sknas
|
cell type: Neuroblastoma cell
cell line: sknas
|
|
Sample_geo_accession | GSM692855
| Sample_status | Public on Mar 16 2013
| Sample_submission_date | Mar 17 2011
| Sample_last_update_date | Mar 16 2013
| 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 | Total RNA was isolated using Trizol (Invitrogen) and purified with RNeasy (Qiagen) according to manufacturer’s protocol
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | RNA sample integrity was checked on an Agilent 2100 Bioanalyzer (Agilent Technologies). 4 µg of total RNA was used for cRNA synthesis and fragmented. Labeling was performed with One-Cycle cDNA synthesis Kit (Affymetrix) according to manufacturer’s protocol. Sample quality was checked on a Bioanalyzer prior and after fragmentation.
| Sample_hyb_protocol | 10 µg of labeled cRNA was hybridized to Affymetrix Human genome U133 Plus 2.0 arrays according to manufacturer’s protocol (Affymetrix).
| Sample_scan_protocol | Arrays were scanned with a GeneChip Scanner 3000 (Affymetrix) according to manufacturer’s protocol
| Sample_data_processing = Expression data (cel files) were normalized with the MAS5.0 algorithm (target signal | 100) using GCOS software (Affymetrix)
| Sample_platform_id | GPL570
| Sample_contact_name | Rogier,,Versteeg
| Sample_contact_email | r.versteeg@amc.uva.nl
| Sample_contact_department | Department of Human Genetics
| Sample_contact_institute | Academic Medical Centre, University of Amsterdam
| Sample_contact_address | P.O. Box 22700
| Sample_contact_city | Amsterdam
| Sample_contact_zip/postal_code | 1100DE
| Sample_contact_country | Netherlands
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM692nnn/GSM692855/suppl/GSM692855.CEL.gz
| Sample_series_id | GSE28019
| Sample_data_row_count | 54675
| |
|
GSM692856 | GPL570 |
|
gimen
|
gimen
|
cell type: Neuroblastoma cell
cell line: gimen
|
|
Sample_geo_accession | GSM692856
| Sample_status | Public on Mar 16 2013
| Sample_submission_date | Mar 17 2011
| Sample_last_update_date | Mar 16 2013
| 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 | Total RNA was isolated using Trizol (Invitrogen) and purified with RNeasy (Qiagen) according to manufacturer’s protocol
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | RNA sample integrity was checked on an Agilent 2100 Bioanalyzer (Agilent Technologies). 4 µg of total RNA was used for cRNA synthesis and fragmented. Labeling was performed with One-Cycle cDNA synthesis Kit (Affymetrix) according to manufacturer’s protocol. Sample quality was checked on a Bioanalyzer prior and after fragmentation.
| Sample_hyb_protocol | 10 µg of labeled cRNA was hybridized to Affymetrix Human genome U133 Plus 2.0 arrays according to manufacturer’s protocol (Affymetrix).
| Sample_scan_protocol | Arrays were scanned with a GeneChip Scanner 3000 (Affymetrix) according to manufacturer’s protocol
| Sample_data_processing = Expression data (cel files) were normalized with the MAS5.0 algorithm (target signal | 100) using GCOS software (Affymetrix)
| Sample_platform_id | GPL570
| Sample_contact_name | Rogier,,Versteeg
| Sample_contact_email | r.versteeg@amc.uva.nl
| Sample_contact_department | Department of Human Genetics
| Sample_contact_institute | Academic Medical Centre, University of Amsterdam
| Sample_contact_address | P.O. Box 22700
| Sample_contact_city | Amsterdam
| Sample_contact_zip/postal_code | 1100DE
| Sample_contact_country | Netherlands
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM692nnn/GSM692856/suppl/GSM692856.CEL.gz
| Sample_series_id | GSE28019
| Sample_data_row_count | 54675
| |
|
GSM692857 | GPL570 |
|
sjnb12
|
sjnb12
|
cell type: Neuroblastoma cell
cell line: sjnb12
|
|
Sample_geo_accession | GSM692857
| Sample_status | Public on Mar 16 2013
| Sample_submission_date | Mar 17 2011
| Sample_last_update_date | Mar 16 2013
| 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 | Total RNA was isolated using Trizol (Invitrogen) and purified with RNeasy (Qiagen) according to manufacturer’s protocol
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | RNA sample integrity was checked on an Agilent 2100 Bioanalyzer (Agilent Technologies). 4 µg of total RNA was used for cRNA synthesis and fragmented. Labeling was performed with One-Cycle cDNA synthesis Kit (Affymetrix) according to manufacturer’s protocol. Sample quality was checked on a Bioanalyzer prior and after fragmentation.
| Sample_hyb_protocol | 10 µg of labeled cRNA was hybridized to Affymetrix Human genome U133 Plus 2.0 arrays according to manufacturer’s protocol (Affymetrix).
| Sample_scan_protocol | Arrays were scanned with a GeneChip Scanner 3000 (Affymetrix) according to manufacturer’s protocol
| Sample_data_processing = Expression data (cel files) were normalized with the MAS5.0 algorithm (target signal | 100) using GCOS software (Affymetrix)
| Sample_platform_id | GPL570
| Sample_contact_name | Rogier,,Versteeg
| Sample_contact_email | r.versteeg@amc.uva.nl
| Sample_contact_department | Department of Human Genetics
| Sample_contact_institute | Academic Medical Centre, University of Amsterdam
| Sample_contact_address | P.O. Box 22700
| Sample_contact_city | Amsterdam
| Sample_contact_zip/postal_code | 1100DE
| Sample_contact_country | Netherlands
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM692nnn/GSM692857/suppl/GSM692857.CEL.gz
| Sample_series_id | GSE28019
| Sample_data_row_count | 54675
| |
|
GSM692858 | GPL570 |
|
shep21n
|
shep21n
|
cell type: Neuroblastoma cell
cell line: shep21n
|
|
Sample_geo_accession | GSM692858
| Sample_status | Public on Mar 16 2013
| Sample_submission_date | Mar 17 2011
| Sample_last_update_date | Mar 16 2013
| 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 | Total RNA was isolated using Trizol (Invitrogen) and purified with RNeasy (Qiagen) according to manufacturer’s protocol
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | RNA sample integrity was checked on an Agilent 2100 Bioanalyzer (Agilent Technologies). 4 µg of total RNA was used for cRNA synthesis and fragmented. Labeling was performed with One-Cycle cDNA synthesis Kit (Affymetrix) according to manufacturer’s protocol. Sample quality was checked on a Bioanalyzer prior and after fragmentation.
| Sample_hyb_protocol | 10 µg of labeled cRNA was hybridized to Affymetrix Human genome U133 Plus 2.0 arrays according to manufacturer’s protocol (Affymetrix).
| Sample_scan_protocol | Arrays were scanned with a GeneChip Scanner 3000 (Affymetrix) according to manufacturer’s protocol
| Sample_data_processing = Expression data (cel files) were normalized with the MAS5.0 algorithm (target signal | 100) using GCOS software (Affymetrix)
| Sample_platform_id | GPL570
| Sample_contact_name | Rogier,,Versteeg
| Sample_contact_email | r.versteeg@amc.uva.nl
| Sample_contact_department | Department of Human Genetics
| Sample_contact_institute | Academic Medical Centre, University of Amsterdam
| Sample_contact_address | P.O. Box 22700
| Sample_contact_city | Amsterdam
| Sample_contact_zip/postal_code | 1100DE
| Sample_contact_country | Netherlands
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM692nnn/GSM692858/suppl/GSM692858.CEL.gz
| Sample_series_id | GSE28019
| Sample_data_row_count | 54675
| |
|
GSM692859 | GPL570 |
|
imr32
|
imr32
|
cell type: Neuroblastoma cell
cell line: imr32
|
|
Sample_geo_accession | GSM692859
| Sample_status | Public on Mar 16 2013
| Sample_submission_date | Mar 17 2011
| Sample_last_update_date | Mar 16 2013
| 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 | Total RNA was isolated using Trizol (Invitrogen) and purified with RNeasy (Qiagen) according to manufacturer’s protocol
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | RNA sample integrity was checked on an Agilent 2100 Bioanalyzer (Agilent Technologies). 4 µg of total RNA was used for cRNA synthesis and fragmented. Labeling was performed with One-Cycle cDNA synthesis Kit (Affymetrix) according to manufacturer’s protocol. Sample quality was checked on a Bioanalyzer prior and after fragmentation.
| Sample_hyb_protocol | 10 µg of labeled cRNA was hybridized to Affymetrix Human genome U133 Plus 2.0 arrays according to manufacturer’s protocol (Affymetrix).
| Sample_scan_protocol | Arrays were scanned with a GeneChip Scanner 3000 (Affymetrix) according to manufacturer’s protocol
| Sample_data_processing = Expression data (cel files) were normalized with the MAS5.0 algorithm (target signal | 100) using GCOS software (Affymetrix)
| Sample_platform_id | GPL570
| Sample_contact_name | Rogier,,Versteeg
| Sample_contact_email | r.versteeg@amc.uva.nl
| Sample_contact_department | Department of Human Genetics
| Sample_contact_institute | Academic Medical Centre, University of Amsterdam
| Sample_contact_address | P.O. Box 22700
| Sample_contact_city | Amsterdam
| Sample_contact_zip/postal_code | 1100DE
| Sample_contact_country | Netherlands
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM692nnn/GSM692859/suppl/GSM692859.CEL.gz
| Sample_series_id | GSE28019
| Sample_data_row_count | 54675
| |
|
GSM692860 | GPL570 |
|
sjnb8
|
sjnb8
|
cell type: Neuroblastoma cell
cell line: sjnb8
|
|
Sample_geo_accession | GSM692860
| Sample_status | Public on Mar 16 2013
| Sample_submission_date | Mar 17 2011
| Sample_last_update_date | Mar 16 2013
| 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 | Total RNA was isolated using Trizol (Invitrogen) and purified with RNeasy (Qiagen) according to manufacturer’s protocol
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | RNA sample integrity was checked on an Agilent 2100 Bioanalyzer (Agilent Technologies). 4 µg of total RNA was used for cRNA synthesis and fragmented. Labeling was performed with One-Cycle cDNA synthesis Kit (Affymetrix) according to manufacturer’s protocol. Sample quality was checked on a Bioanalyzer prior and after fragmentation.
| Sample_hyb_protocol | 10 µg of labeled cRNA was hybridized to Affymetrix Human genome U133 Plus 2.0 arrays according to manufacturer’s protocol (Affymetrix).
| Sample_scan_protocol | Arrays were scanned with a GeneChip Scanner 3000 (Affymetrix) according to manufacturer’s protocol
| Sample_data_processing = Expression data (cel files) were normalized with the MAS5.0 algorithm (target signal | 100) using GCOS software (Affymetrix)
| Sample_platform_id | GPL570
| Sample_contact_name | Rogier,,Versteeg
| Sample_contact_email | r.versteeg@amc.uva.nl
| Sample_contact_department | Department of Human Genetics
| Sample_contact_institute | Academic Medical Centre, University of Amsterdam
| Sample_contact_address | P.O. Box 22700
| Sample_contact_city | Amsterdam
| Sample_contact_zip/postal_code | 1100DE
| Sample_contact_country | Netherlands
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM692nnn/GSM692860/suppl/GSM692860.CEL.gz
| Sample_series_id | GSE28019
| Sample_data_row_count | 54675
| |
|
GSM692861 | GPL570 |
|
sjnb10
|
sjnb10
|
cell type: Neuroblastoma cell
cell line: sjnb10
|
|
Sample_geo_accession | GSM692861
| Sample_status | Public on Mar 16 2013
| Sample_submission_date | Mar 17 2011
| Sample_last_update_date | Mar 16 2013
| 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 | Total RNA was isolated using Trizol (Invitrogen) and purified with RNeasy (Qiagen) according to manufacturer’s protocol
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | RNA sample integrity was checked on an Agilent 2100 Bioanalyzer (Agilent Technologies). 4 µg of total RNA was used for cRNA synthesis and fragmented. Labeling was performed with One-Cycle cDNA synthesis Kit (Affymetrix) according to manufacturer’s protocol. Sample quality was checked on a Bioanalyzer prior and after fragmentation.
| Sample_hyb_protocol | 10 µg of labeled cRNA was hybridized to Affymetrix Human genome U133 Plus 2.0 arrays according to manufacturer’s protocol (Affymetrix).
| Sample_scan_protocol | Arrays were scanned with a GeneChip Scanner 3000 (Affymetrix) according to manufacturer’s protocol
| Sample_data_processing = Expression data (cel files) were normalized with the MAS5.0 algorithm (target signal | 100) using GCOS software (Affymetrix)
| Sample_platform_id | GPL570
| Sample_contact_name | Rogier,,Versteeg
| Sample_contact_email | r.versteeg@amc.uva.nl
| Sample_contact_department | Department of Human Genetics
| Sample_contact_institute | Academic Medical Centre, University of Amsterdam
| Sample_contact_address | P.O. Box 22700
| Sample_contact_city | Amsterdam
| Sample_contact_zip/postal_code | 1100DE
| Sample_contact_country | Netherlands
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM692nnn/GSM692861/suppl/GSM692861.CEL.gz
| Sample_series_id | GSE28019
| Sample_data_row_count | 54675
| |
|
GSM692862 | GPL570 |
|
nmb
|
nmb
|
cell type: Neuroblastoma cell
cell line: nmb
|
|
Sample_geo_accession | GSM692862
| Sample_status | Public on Mar 16 2013
| Sample_submission_date | Mar 17 2011
| Sample_last_update_date | Mar 16 2013
| 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 | Total RNA was isolated using Trizol (Invitrogen) and purified with RNeasy (Qiagen) according to manufacturer’s protocol
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | RNA sample integrity was checked on an Agilent 2100 Bioanalyzer (Agilent Technologies). 4 µg of total RNA was used for cRNA synthesis and fragmented. Labeling was performed with One-Cycle cDNA synthesis Kit (Affymetrix) according to manufacturer’s protocol. Sample quality was checked on a Bioanalyzer prior and after fragmentation.
| Sample_hyb_protocol | 10 µg of labeled cRNA was hybridized to Affymetrix Human genome U133 Plus 2.0 arrays according to manufacturer’s protocol (Affymetrix).
| Sample_scan_protocol | Arrays were scanned with a GeneChip Scanner 3000 (Affymetrix) according to manufacturer’s protocol
| Sample_data_processing = Expression data (cel files) were normalized with the MAS5.0 algorithm (target signal | 100) using GCOS software (Affymetrix)
| Sample_platform_id | GPL570
| Sample_contact_name | Rogier,,Versteeg
| Sample_contact_email | r.versteeg@amc.uva.nl
| Sample_contact_department | Department of Human Genetics
| Sample_contact_institute | Academic Medical Centre, University of Amsterdam
| Sample_contact_address | P.O. Box 22700
| Sample_contact_city | Amsterdam
| Sample_contact_zip/postal_code | 1100DE
| Sample_contact_country | Netherlands
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM692nnn/GSM692862/suppl/GSM692862.CEL.gz
| Sample_series_id | GSE28019
| Sample_data_row_count | 54675
| |
|
GSM692863 | GPL570 |
|
chp134
|
chp134
|
cell type: Neuroblastoma cell
cell line: chp134
|
|
Sample_geo_accession | GSM692863
| Sample_status | Public on Mar 16 2013
| Sample_submission_date | Mar 17 2011
| Sample_last_update_date | Mar 16 2013
| 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 | Total RNA was isolated using Trizol (Invitrogen) and purified with RNeasy (Qiagen) according to manufacturer’s protocol
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | RNA sample integrity was checked on an Agilent 2100 Bioanalyzer (Agilent Technologies). 4 µg of total RNA was used for cRNA synthesis and fragmented. Labeling was performed with One-Cycle cDNA synthesis Kit (Affymetrix) according to manufacturer’s protocol. Sample quality was checked on a Bioanalyzer prior and after fragmentation.
| Sample_hyb_protocol | 10 µg of labeled cRNA was hybridized to Affymetrix Human genome U133 Plus 2.0 arrays according to manufacturer’s protocol (Affymetrix).
| Sample_scan_protocol | Arrays were scanned with a GeneChip Scanner 3000 (Affymetrix) according to manufacturer’s protocol
| Sample_data_processing = Expression data (cel files) were normalized with the MAS5.0 algorithm (target signal | 100) using GCOS software (Affymetrix)
| Sample_platform_id | GPL570
| Sample_contact_name | Rogier,,Versteeg
| Sample_contact_email | r.versteeg@amc.uva.nl
| Sample_contact_department | Department of Human Genetics
| Sample_contact_institute | Academic Medical Centre, University of Amsterdam
| Sample_contact_address | P.O. Box 22700
| Sample_contact_city | Amsterdam
| Sample_contact_zip/postal_code | 1100DE
| Sample_contact_country | Netherlands
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM692nnn/GSM692863/suppl/GSM692863.CEL.gz
| Sample_series_id | GSE28019
| Sample_data_row_count | 54675
| |
|
GSM692864 | GPL570 |
|
sknsh
|
sknsh
|
cell type: Neuroblastoma cell
cell line: sknsh
|
|
Sample_geo_accession | GSM692864
| Sample_status | Public on Mar 16 2013
| Sample_submission_date | Mar 17 2011
| Sample_last_update_date | Mar 16 2013
| 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 | Total RNA was isolated using Trizol (Invitrogen) and purified with RNeasy (Qiagen) according to manufacturer’s protocol
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | RNA sample integrity was checked on an Agilent 2100 Bioanalyzer (Agilent Technologies). 4 µg of total RNA was used for cRNA synthesis and fragmented. Labeling was performed with One-Cycle cDNA synthesis Kit (Affymetrix) according to manufacturer’s protocol. Sample quality was checked on a Bioanalyzer prior and after fragmentation.
| Sample_hyb_protocol | 10 µg of labeled cRNA was hybridized to Affymetrix Human genome U133 Plus 2.0 arrays according to manufacturer’s protocol (Affymetrix).
| Sample_scan_protocol | Arrays were scanned with a GeneChip Scanner 3000 (Affymetrix) according to manufacturer’s protocol
| Sample_data_processing = Expression data (cel files) were normalized with the MAS5.0 algorithm (target signal | 100) using GCOS software (Affymetrix)
| Sample_platform_id | GPL570
| Sample_contact_name | Rogier,,Versteeg
| Sample_contact_email | r.versteeg@amc.uva.nl
| Sample_contact_department | Department of Human Genetics
| Sample_contact_institute | Academic Medical Centre, University of Amsterdam
| Sample_contact_address | P.O. Box 22700
| Sample_contact_city | Amsterdam
| Sample_contact_zip/postal_code | 1100DE
| Sample_contact_country | Netherlands
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM692nnn/GSM692864/suppl/GSM692864.CEL.gz
| Sample_series_id | GSE28019
| Sample_data_row_count | 54675
| |
|
GSM692865 | GPL570 |
|
ngp
|
ngp
|
cell type: Neuroblastoma cell
cell line: ngp
|
|
Sample_geo_accession | GSM692865
| Sample_status | Public on Mar 16 2013
| Sample_submission_date | Mar 17 2011
| Sample_last_update_date | Mar 16 2013
| 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 | Total RNA was isolated using Trizol (Invitrogen) and purified with RNeasy (Qiagen) according to manufacturer’s protocol
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | RNA sample integrity was checked on an Agilent 2100 Bioanalyzer (Agilent Technologies). 4 µg of total RNA was used for cRNA synthesis and fragmented. Labeling was performed with One-Cycle cDNA synthesis Kit (Affymetrix) according to manufacturer’s protocol. Sample quality was checked on a Bioanalyzer prior and after fragmentation.
| Sample_hyb_protocol | 10 µg of labeled cRNA was hybridized to Affymetrix Human genome U133 Plus 2.0 arrays according to manufacturer’s protocol (Affymetrix).
| Sample_scan_protocol | Arrays were scanned with a GeneChip Scanner 3000 (Affymetrix) according to manufacturer’s protocol
| Sample_data_processing = Expression data (cel files) were normalized with the MAS5.0 algorithm (target signal | 100) using GCOS software (Affymetrix)
| Sample_platform_id | GPL570
| Sample_contact_name | Rogier,,Versteeg
| Sample_contact_email | r.versteeg@amc.uva.nl
| Sample_contact_department | Department of Human Genetics
| Sample_contact_institute | Academic Medical Centre, University of Amsterdam
| Sample_contact_address | P.O. Box 22700
| Sample_contact_city | Amsterdam
| Sample_contact_zip/postal_code | 1100DE
| Sample_contact_country | Netherlands
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM692nnn/GSM692865/suppl/GSM692865.CEL.gz
| Sample_series_id | GSE28019
| Sample_data_row_count | 54675
| |
|
GSM692866 | GPL570 |
|
smskcnr
|
smskcnr
|
cell type: Neuroblastoma cell
cell line: smskcnr
|
|
Sample_geo_accession | GSM692866
| Sample_status | Public on Mar 16 2013
| Sample_submission_date | Mar 17 2011
| Sample_last_update_date | Mar 16 2013
| 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 | Total RNA was isolated using Trizol (Invitrogen) and purified with RNeasy (Qiagen) according to manufacturer’s protocol
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | RNA sample integrity was checked on an Agilent 2100 Bioanalyzer (Agilent Technologies). 4 µg of total RNA was used for cRNA synthesis and fragmented. Labeling was performed with One-Cycle cDNA synthesis Kit (Affymetrix) according to manufacturer’s protocol. Sample quality was checked on a Bioanalyzer prior and after fragmentation.
| Sample_hyb_protocol | 10 µg of labeled cRNA was hybridized to Affymetrix Human genome U133 Plus 2.0 arrays according to manufacturer’s protocol (Affymetrix).
| Sample_scan_protocol | Arrays were scanned with a GeneChip Scanner 3000 (Affymetrix) according to manufacturer’s protocol
| Sample_data_processing = Expression data (cel files) were normalized with the MAS5.0 algorithm (target signal | 100) using GCOS software (Affymetrix)
| Sample_platform_id | GPL570
| Sample_contact_name | Rogier,,Versteeg
| Sample_contact_email | r.versteeg@amc.uva.nl
| Sample_contact_department | Department of Human Genetics
| Sample_contact_institute | Academic Medical Centre, University of Amsterdam
| Sample_contact_address | P.O. Box 22700
| Sample_contact_city | Amsterdam
| Sample_contact_zip/postal_code | 1100DE
| Sample_contact_country | Netherlands
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM692nnn/GSM692866/suppl/GSM692866.CEL.gz
| Sample_series_id | GSE28019
| Sample_data_row_count | 54675
| |
|
GSM692867 | GPL570 |
|
n206
|
n206
|
cell type: Neuroblastoma cell
cell line: n206
|
|
Sample_geo_accession | GSM692867
| Sample_status | Public on Mar 16 2013
| Sample_submission_date | Mar 17 2011
| Sample_last_update_date | Mar 16 2013
| 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 | Total RNA was isolated using Trizol (Invitrogen) and purified with RNeasy (Qiagen) according to manufacturer’s protocol
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | RNA sample integrity was checked on an Agilent 2100 Bioanalyzer (Agilent Technologies). 4 µg of total RNA was used for cRNA synthesis and fragmented. Labeling was performed with One-Cycle cDNA synthesis Kit (Affymetrix) according to manufacturer’s protocol. Sample quality was checked on a Bioanalyzer prior and after fragmentation.
| Sample_hyb_protocol | 10 µg of labeled cRNA was hybridized to Affymetrix Human genome U133 Plus 2.0 arrays according to manufacturer’s protocol (Affymetrix).
| Sample_scan_protocol | Arrays were scanned with a GeneChip Scanner 3000 (Affymetrix) according to manufacturer’s protocol
| Sample_data_processing = Expression data (cel files) were normalized with the MAS5.0 algorithm (target signal | 100) using GCOS software (Affymetrix)
| Sample_platform_id | GPL570
| Sample_contact_name | Rogier,,Versteeg
| Sample_contact_email | r.versteeg@amc.uva.nl
| Sample_contact_department | Department of Human Genetics
| Sample_contact_institute | Academic Medical Centre, University of Amsterdam
| Sample_contact_address | P.O. Box 22700
| Sample_contact_city | Amsterdam
| Sample_contact_zip/postal_code | 1100DE
| Sample_contact_country | Netherlands
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM692nnn/GSM692867/suppl/GSM692867.CEL.gz
| Sample_series_id | GSE28019
| Sample_data_row_count | 54675
| |
|
GSM692868 | GPL570 |
|
tr14
|
tr14
|
cell type: Neuroblastoma cell
cell line: tr14
|
|
Sample_geo_accession | GSM692868
| Sample_status | Public on Mar 16 2013
| Sample_submission_date | Mar 17 2011
| Sample_last_update_date | Mar 16 2013
| 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 | Total RNA was isolated using Trizol (Invitrogen) and purified with RNeasy (Qiagen) according to manufacturer’s protocol
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | RNA sample integrity was checked on an Agilent 2100 Bioanalyzer (Agilent Technologies). 4 µg of total RNA was used for cRNA synthesis and fragmented. Labeling was performed with One-Cycle cDNA synthesis Kit (Affymetrix) according to manufacturer’s protocol. Sample quality was checked on a Bioanalyzer prior and after fragmentation.
| Sample_hyb_protocol | 10 µg of labeled cRNA was hybridized to Affymetrix Human genome U133 Plus 2.0 arrays according to manufacturer’s protocol (Affymetrix).
| Sample_scan_protocol | Arrays were scanned with a GeneChip Scanner 3000 (Affymetrix) according to manufacturer’s protocol
| Sample_data_processing = Expression data (cel files) were normalized with the MAS5.0 algorithm (target signal | 100) using GCOS software (Affymetrix)
| Sample_platform_id | GPL570
| Sample_contact_name | Rogier,,Versteeg
| Sample_contact_email | r.versteeg@amc.uva.nl
| Sample_contact_department | Department of Human Genetics
| Sample_contact_institute | Academic Medical Centre, University of Amsterdam
| Sample_contact_address | P.O. Box 22700
| Sample_contact_city | Amsterdam
| Sample_contact_zip/postal_code | 1100DE
| Sample_contact_country | Netherlands
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM692nnn/GSM692868/suppl/GSM692868.CEL.gz
| Sample_series_id | GSE28019
| Sample_data_row_count | 54675
| |
|
GSM692869 | GPL570 |
|
sknbe
|
sknbe
|
cell type: Neuroblastoma cell
cell line: sknbe
|
|
Sample_geo_accession | GSM692869
| Sample_status | Public on Mar 16 2013
| Sample_submission_date | Mar 17 2011
| Sample_last_update_date | Mar 16 2013
| 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 | Total RNA was isolated using Trizol (Invitrogen) and purified with RNeasy (Qiagen) according to manufacturer’s protocol
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | RNA sample integrity was checked on an Agilent 2100 Bioanalyzer (Agilent Technologies). 4 µg of total RNA was used for cRNA synthesis and fragmented. Labeling was performed with One-Cycle cDNA synthesis Kit (Affymetrix) according to manufacturer’s protocol. Sample quality was checked on a Bioanalyzer prior and after fragmentation.
| Sample_hyb_protocol | 10 µg of labeled cRNA was hybridized to Affymetrix Human genome U133 Plus 2.0 arrays according to manufacturer’s protocol (Affymetrix).
| Sample_scan_protocol | Arrays were scanned with a GeneChip Scanner 3000 (Affymetrix) according to manufacturer’s protocol
| Sample_data_processing = Expression data (cel files) were normalized with the MAS5.0 algorithm (target signal | 100) using GCOS software (Affymetrix)
| Sample_platform_id | GPL570
| Sample_contact_name | Rogier,,Versteeg
| Sample_contact_email | r.versteeg@amc.uva.nl
| Sample_contact_department | Department of Human Genetics
| Sample_contact_institute | Academic Medical Centre, University of Amsterdam
| Sample_contact_address | P.O. Box 22700
| Sample_contact_city | Amsterdam
| Sample_contact_zip/postal_code | 1100DE
| Sample_contact_country | Netherlands
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM692nnn/GSM692869/suppl/GSM692869.CEL.gz
| Sample_series_id | GSE28019
| Sample_data_row_count | 54675
| |
|
GSM692870 | GPL570 |
|
sjnb1
|
sjnb1
|
cell type: Neuroblastoma cell
cell line: sjnb1
|
|
Sample_geo_accession | GSM692870
| Sample_status | Public on Mar 16 2013
| Sample_submission_date | Mar 17 2011
| Sample_last_update_date | Mar 16 2013
| 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 | Total RNA was isolated using Trizol (Invitrogen) and purified with RNeasy (Qiagen) according to manufacturer’s protocol
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | RNA sample integrity was checked on an Agilent 2100 Bioanalyzer (Agilent Technologies). 4 µg of total RNA was used for cRNA synthesis and fragmented. Labeling was performed with One-Cycle cDNA synthesis Kit (Affymetrix) according to manufacturer’s protocol. Sample quality was checked on a Bioanalyzer prior and after fragmentation.
| Sample_hyb_protocol | 10 µg of labeled cRNA was hybridized to Affymetrix Human genome U133 Plus 2.0 arrays according to manufacturer’s protocol (Affymetrix).
| Sample_scan_protocol | Arrays were scanned with a GeneChip Scanner 3000 (Affymetrix) according to manufacturer’s protocol
| Sample_data_processing = Expression data (cel files) were normalized with the MAS5.0 algorithm (target signal | 100) using GCOS software (Affymetrix)
| Sample_platform_id | GPL570
| Sample_contact_name | Rogier,,Versteeg
| Sample_contact_email | r.versteeg@amc.uva.nl
| Sample_contact_department | Department of Human Genetics
| Sample_contact_institute | Academic Medical Centre, University of Amsterdam
| Sample_contact_address | P.O. Box 22700
| Sample_contact_city | Amsterdam
| Sample_contact_zip/postal_code | 1100DE
| Sample_contact_country | Netherlands
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM692nnn/GSM692870/suppl/GSM692870.CEL.gz
| Sample_series_id | GSE28019
| Sample_data_row_count | 54675
| |
|
GSM692871 | GPL570 |
|
lan5
|
lan5
|
cell type: Neuroblastoma cell
cell line: lan5
|
|
Sample_geo_accession | GSM692871
| Sample_status | Public on Mar 16 2013
| Sample_submission_date | Mar 17 2011
| Sample_last_update_date | Mar 16 2013
| 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 | Total RNA was isolated using Trizol (Invitrogen) and purified with RNeasy (Qiagen) according to manufacturer’s protocol
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | RNA sample integrity was checked on an Agilent 2100 Bioanalyzer (Agilent Technologies). 4 µg of total RNA was used for cRNA synthesis and fragmented. Labeling was performed with One-Cycle cDNA synthesis Kit (Affymetrix) according to manufacturer’s protocol. Sample quality was checked on a Bioanalyzer prior and after fragmentation.
| Sample_hyb_protocol | 10 µg of labeled cRNA was hybridized to Affymetrix Human genome U133 Plus 2.0 arrays according to manufacturer’s protocol (Affymetrix).
| Sample_scan_protocol | Arrays were scanned with a GeneChip Scanner 3000 (Affymetrix) according to manufacturer’s protocol
| Sample_data_processing = Expression data (cel files) were normalized with the MAS5.0 algorithm (target signal | 100) using GCOS software (Affymetrix)
| Sample_platform_id | GPL570
| Sample_contact_name | Rogier,,Versteeg
| Sample_contact_email | r.versteeg@amc.uva.nl
| Sample_contact_department | Department of Human Genetics
| Sample_contact_institute | Academic Medical Centre, University of Amsterdam
| Sample_contact_address | P.O. Box 22700
| Sample_contact_city | Amsterdam
| Sample_contact_zip/postal_code | 1100DE
| Sample_contact_country | Netherlands
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM692nnn/GSM692871/suppl/GSM692871.CEL.gz
| Sample_series_id | GSE28019
| Sample_data_row_count | 54675
| |
|
GSM692872 | GPL570 |
|
lan1
|
lan1
|
cell type: Neuroblastoma cell
cell line: lan1
|
|
Sample_geo_accession | GSM692872
| Sample_status | Public on Mar 16 2013
| Sample_submission_date | Mar 17 2011
| Sample_last_update_date | Mar 16 2013
| 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 | Total RNA was isolated using Trizol (Invitrogen) and purified with RNeasy (Qiagen) according to manufacturer’s protocol
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | RNA sample integrity was checked on an Agilent 2100 Bioanalyzer (Agilent Technologies). 4 µg of total RNA was used for cRNA synthesis and fragmented. Labeling was performed with One-Cycle cDNA synthesis Kit (Affymetrix) according to manufacturer’s protocol. Sample quality was checked on a Bioanalyzer prior and after fragmentation.
| Sample_hyb_protocol | 10 µg of labeled cRNA was hybridized to Affymetrix Human genome U133 Plus 2.0 arrays according to manufacturer’s protocol (Affymetrix).
| Sample_scan_protocol | Arrays were scanned with a GeneChip Scanner 3000 (Affymetrix) according to manufacturer’s protocol
| Sample_data_processing = Expression data (cel files) were normalized with the MAS5.0 algorithm (target signal | 100) using GCOS software (Affymetrix)
| Sample_platform_id | GPL570
| Sample_contact_name | Rogier,,Versteeg
| Sample_contact_email | r.versteeg@amc.uva.nl
| Sample_contact_department | Department of Human Genetics
| Sample_contact_institute | Academic Medical Centre, University of Amsterdam
| Sample_contact_address | P.O. Box 22700
| Sample_contact_city | Amsterdam
| Sample_contact_zip/postal_code | 1100DE
| Sample_contact_country | Netherlands
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM692nnn/GSM692872/suppl/GSM692872.CEL.gz
| Sample_series_id | GSE28019
| Sample_data_row_count | 54675
| |
|
GSM692873 | GPL570 |
|
amc106
|
amc106
|
cell type: Neuroblastoma cell
cell line: amc106
|
|
Sample_geo_accession | GSM692873
| Sample_status | Public on Mar 16 2013
| Sample_submission_date | Mar 17 2011
| Sample_last_update_date | Mar 16 2013
| 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 | Total RNA was isolated using Trizol (Invitrogen) and purified with RNeasy (Qiagen) according to manufacturer’s protocol
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | RNA sample integrity was checked on an Agilent 2100 Bioanalyzer (Agilent Technologies). 4 µg of total RNA was used for cRNA synthesis and fragmented. Labeling was performed with One-Cycle cDNA synthesis Kit (Affymetrix) according to manufacturer’s protocol. Sample quality was checked on a Bioanalyzer prior and after fragmentation.
| Sample_hyb_protocol | 10 µg of labeled cRNA was hybridized to Affymetrix Human genome U133 Plus 2.0 arrays according to manufacturer’s protocol (Affymetrix).
| Sample_scan_protocol | Arrays were scanned with a GeneChip Scanner 3000 (Affymetrix) according to manufacturer’s protocol
| Sample_data_processing = Expression data (cel files) were normalized with the MAS5.0 algorithm (target signal | 100) using GCOS software (Affymetrix)
| Sample_platform_id | GPL570
| Sample_contact_name | Rogier,,Versteeg
| Sample_contact_email | r.versteeg@amc.uva.nl
| Sample_contact_department | Department of Human Genetics
| Sample_contact_institute | Academic Medical Centre, University of Amsterdam
| Sample_contact_address | P.O. Box 22700
| Sample_contact_city | Amsterdam
| Sample_contact_zip/postal_code | 1100DE
| Sample_contact_country | Netherlands
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM692nnn/GSM692873/suppl/GSM692873.CEL.gz
| Sample_series_id | GSE28019
| Sample_data_row_count | 54675
| |
|
GSM692874 | GPL570 |
|
shsy5y
|
shsy5y
|
cell type: Neuroblastoma cell
cell line: shsy5y
|
|
Sample_geo_accession | GSM692874
| Sample_status | Public on Mar 16 2013
| Sample_submission_date | Mar 17 2011
| Sample_last_update_date | Mar 16 2013
| 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 | Total RNA was isolated using Trizol (Invitrogen) and purified with RNeasy (Qiagen) according to manufacturer’s protocol
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | RNA sample integrity was checked on an Agilent 2100 Bioanalyzer (Agilent Technologies). 4 µg of total RNA was used for cRNA synthesis and fragmented. Labeling was performed with One-Cycle cDNA synthesis Kit (Affymetrix) according to manufacturer’s protocol. Sample quality was checked on a Bioanalyzer prior and after fragmentation.
| Sample_hyb_protocol | 10 µg of labeled cRNA was hybridized to Affymetrix Human genome U133 Plus 2.0 arrays according to manufacturer’s protocol (Affymetrix).
| Sample_scan_protocol | Arrays were scanned with a GeneChip Scanner 3000 (Affymetrix) according to manufacturer’s protocol
| Sample_data_processing = Expression data (cel files) were normalized with the MAS5.0 algorithm (target signal | 100) using GCOS software (Affymetrix)
| Sample_platform_id | GPL570
| Sample_contact_name | Rogier,,Versteeg
| Sample_contact_email | r.versteeg@amc.uva.nl
| Sample_contact_department | Department of Human Genetics
| Sample_contact_institute | Academic Medical Centre, University of Amsterdam
| Sample_contact_address | P.O. Box 22700
| Sample_contact_city | Amsterdam
| Sample_contact_zip/postal_code | 1100DE
| Sample_contact_country | Netherlands
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM692nnn/GSM692874/suppl/GSM692874.CEL.gz
| Sample_series_id | GSE28019
| Sample_data_row_count | 54675
| |
|
GSM692875 | GPL570 |
|
shep2
|
shep2
|
cell type: Neuroblastoma cell
cell line: shep2
|
|
Sample_geo_accession | GSM692875
| Sample_status | Public on Mar 16 2013
| Sample_submission_date | Mar 17 2011
| Sample_last_update_date | Mar 16 2013
| 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 | Total RNA was isolated using Trizol (Invitrogen) and purified with RNeasy (Qiagen) according to manufacturer’s protocol
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | RNA sample integrity was checked on an Agilent 2100 Bioanalyzer (Agilent Technologies). 4 µg of total RNA was used for cRNA synthesis and fragmented. Labeling was performed with One-Cycle cDNA synthesis Kit (Affymetrix) according to manufacturer’s protocol. Sample quality was checked on a Bioanalyzer prior and after fragmentation.
| Sample_hyb_protocol | 10 µg of labeled cRNA was hybridized to Affymetrix Human genome U133 Plus 2.0 arrays according to manufacturer’s protocol (Affymetrix).
| Sample_scan_protocol | Arrays were scanned with a GeneChip Scanner 3000 (Affymetrix) according to manufacturer’s protocol
| Sample_data_processing = Expression data (cel files) were normalized with the MAS5.0 algorithm (target signal | 100) using GCOS software (Affymetrix)
| Sample_platform_id | GPL570
| Sample_contact_name | Rogier,,Versteeg
| Sample_contact_email | r.versteeg@amc.uva.nl
| Sample_contact_department | Department of Human Genetics
| Sample_contact_institute | Academic Medical Centre, University of Amsterdam
| Sample_contact_address | P.O. Box 22700
| Sample_contact_city | Amsterdam
| Sample_contact_zip/postal_code | 1100DE
| Sample_contact_country | Netherlands
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM692nnn/GSM692875/suppl/GSM692875.CEL.gz
| Sample_series_id | GSE28019
| Sample_data_row_count | 54675
| |
|
GSM692876 | GPL570 |
|
uhgnp
|
uhgnp
|
cell type: Neuroblastoma cell
cell line: uhgnp
|
|
Sample_geo_accession | GSM692876
| Sample_status | Public on Mar 16 2013
| Sample_submission_date | Mar 17 2011
| Sample_last_update_date | Mar 16 2013
| 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 | Total RNA was isolated using Trizol (Invitrogen) and purified with RNeasy (Qiagen) according to manufacturer’s protocol
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | RNA sample integrity was checked on an Agilent 2100 Bioanalyzer (Agilent Technologies). 4 µg of total RNA was used for cRNA synthesis and fragmented. Labeling was performed with One-Cycle cDNA synthesis Kit (Affymetrix) according to manufacturer’s protocol. Sample quality was checked on a Bioanalyzer prior and after fragmentation.
| Sample_hyb_protocol | 10 µg of labeled cRNA was hybridized to Affymetrix Human genome U133 Plus 2.0 arrays according to manufacturer’s protocol (Affymetrix).
| Sample_scan_protocol | Arrays were scanned with a GeneChip Scanner 3000 (Affymetrix) according to manufacturer’s protocol
| Sample_data_processing = Expression data (cel files) were normalized with the MAS5.0 algorithm (target signal | 100) using GCOS software (Affymetrix)
| Sample_platform_id | GPL570
| Sample_contact_name | Rogier,,Versteeg
| Sample_contact_email | r.versteeg@amc.uva.nl
| Sample_contact_department | Department of Human Genetics
| Sample_contact_institute | Academic Medical Centre, University of Amsterdam
| Sample_contact_address | P.O. Box 22700
| Sample_contact_city | Amsterdam
| Sample_contact_zip/postal_code | 1100DE
| Sample_contact_country | Netherlands
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM692nnn/GSM692876/suppl/GSM692876.CEL.gz
| Sample_series_id | GSE28019
| Sample_data_row_count | 54675
| |
|
GSM692877 | GPL570 |
|
sjnb6
|
sjnb6
|
cell type: Neuroblastoma cell
cell line: sjnb6
|
|
Sample_geo_accession | GSM692877
| Sample_status | Public on Mar 16 2013
| Sample_submission_date | Mar 17 2011
| Sample_last_update_date | Mar 16 2013
| 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 | Total RNA was isolated using Trizol (Invitrogen) and purified with RNeasy (Qiagen) according to manufacturer’s protocol
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | RNA sample integrity was checked on an Agilent 2100 Bioanalyzer (Agilent Technologies). 4 µg of total RNA was used for cRNA synthesis and fragmented. Labeling was performed with One-Cycle cDNA synthesis Kit (Affymetrix) according to manufacturer’s protocol. Sample quality was checked on a Bioanalyzer prior and after fragmentation.
| Sample_hyb_protocol | 10 µg of labeled cRNA was hybridized to Affymetrix Human genome U133 Plus 2.0 arrays according to manufacturer’s protocol (Affymetrix).
| Sample_scan_protocol | Arrays were scanned with a GeneChip Scanner 3000 (Affymetrix) according to manufacturer’s protocol
| Sample_data_processing = Expression data (cel files) were normalized with the MAS5.0 algorithm (target signal | 100) using GCOS software (Affymetrix)
| Sample_platform_id | GPL570
| Sample_contact_name | Rogier,,Versteeg
| Sample_contact_email | r.versteeg@amc.uva.nl
| Sample_contact_department | Department of Human Genetics
| Sample_contact_institute | Academic Medical Centre, University of Amsterdam
| Sample_contact_address | P.O. Box 22700
| Sample_contact_city | Amsterdam
| Sample_contact_zip/postal_code | 1100DE
| Sample_contact_country | Netherlands
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM692nnn/GSM692877/suppl/GSM692877.CEL.gz
| Sample_series_id | GSE28019
| Sample_data_row_count | 54675
| |
|
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Select GSMs and click on "Add groups" |
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