Search results for the GEO ID: GSE45270 |
(Click on the check boxes provided under "Select for analysis", to initiate grouping) |
(Once the selection is made, click on "Add groups" in "Make groups for comparison", to make a group. Scroll down) |
|
GSM ID | GPL ID |
Select for analysis |
Title |
Source name |
Description |
Characteristics |
GSM1100483 | GPL570 |
|
Tubular Adenoma, sample 1
|
tubular adenoma
|
tissue: tubular adenoma
|
fap1
|
Sample_geo_accession | GSM1100483
| Sample_status | Public on Apr 14 2013
| Sample_submission_date | Mar 18 2013
| Sample_last_update_date | Apr 14 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 the 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 the One-Cycle cDNA synthesis Kit (Affymetrix) according to the 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 the manufacturer's protocol (Affymetrix).
| Sample_scan_protocol | Arrays were scanned with a GeneChip Scanner 3000 (Affymetrix) according to the 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/GSM1100nnn/GSM1100483/suppl/GSM1100483_EXT_423.CEL.gz
| Sample_series_id | GSE45270
| Sample_data_row_count | 34549
| |
|
GSM1100484 | GPL570 |
|
Tubular Adenoma, sample 2
|
tubular adenoma
|
tissue: tubular adenoma
|
fap2
|
Sample_geo_accession | GSM1100484
| Sample_status | Public on Apr 14 2013
| Sample_submission_date | Mar 18 2013
| Sample_last_update_date | Apr 14 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 the 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 the One-Cycle cDNA synthesis Kit (Affymetrix) according to the 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 the manufacturer's protocol (Affymetrix).
| Sample_scan_protocol | Arrays were scanned with a GeneChip Scanner 3000 (Affymetrix) according to the 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/GSM1100nnn/GSM1100484/suppl/GSM1100484_EXT_424.CEL.gz
| Sample_series_id | GSE45270
| Sample_data_row_count | 34549
| |
|
GSM1100485 | GPL570 |
|
Tubular Adenoma, sample 3
|
tubular adenoma
|
tissue: tubular adenoma
|
fap3
|
Sample_geo_accession | GSM1100485
| Sample_status | Public on Apr 14 2013
| Sample_submission_date | Mar 18 2013
| Sample_last_update_date | Apr 14 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 the 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 the One-Cycle cDNA synthesis Kit (Affymetrix) according to the 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 the manufacturer's protocol (Affymetrix).
| Sample_scan_protocol | Arrays were scanned with a GeneChip Scanner 3000 (Affymetrix) according to the 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/GSM1100nnn/GSM1100485/suppl/GSM1100485_EXT_425.CEL.gz
| Sample_series_id | GSE45270
| Sample_data_row_count | 34549
| |
|
GSM1100486 | GPL570 |
|
Tubular Adenoma, sample 4
|
tubular adenoma
|
tissue: tubular adenoma
|
fap4
|
Sample_geo_accession | GSM1100486
| Sample_status | Public on Apr 14 2013
| Sample_submission_date | Mar 18 2013
| Sample_last_update_date | Apr 14 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 the 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 the One-Cycle cDNA synthesis Kit (Affymetrix) according to the 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 the manufacturer's protocol (Affymetrix).
| Sample_scan_protocol | Arrays were scanned with a GeneChip Scanner 3000 (Affymetrix) according to the 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/GSM1100nnn/GSM1100486/suppl/GSM1100486_EXT_426.CEL.gz
| Sample_series_id | GSE45270
| Sample_data_row_count | 34549
| |
|
GSM1100487 | GPL570 |
|
Tubular Adenoma, sample 5
|
tubular adenoma
|
tissue: tubular adenoma
|
fap5
|
Sample_geo_accession | GSM1100487
| Sample_status | Public on Apr 14 2013
| Sample_submission_date | Mar 18 2013
| Sample_last_update_date | Apr 14 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 the 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 the One-Cycle cDNA synthesis Kit (Affymetrix) according to the 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 the manufacturer's protocol (Affymetrix).
| Sample_scan_protocol | Arrays were scanned with a GeneChip Scanner 3000 (Affymetrix) according to the 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/GSM1100nnn/GSM1100487/suppl/GSM1100487_EXT_427.CEL.gz
| Sample_series_id | GSE45270
| Sample_data_row_count | 34549
| |
|
GSM1100488 | GPL570 |
|
Tubular Adenoma, sample 6
|
tubular adenoma
|
tissue: tubular adenoma
|
fap6
|
Sample_geo_accession | GSM1100488
| Sample_status | Public on Apr 14 2013
| Sample_submission_date | Mar 18 2013
| Sample_last_update_date | Apr 14 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 the 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 the One-Cycle cDNA synthesis Kit (Affymetrix) according to the 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 the manufacturer's protocol (Affymetrix).
| Sample_scan_protocol | Arrays were scanned with a GeneChip Scanner 3000 (Affymetrix) according to the 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/GSM1100nnn/GSM1100488/suppl/GSM1100488_EXT_428.CEL.gz
| Sample_series_id | GSE45270
| Sample_data_row_count | 34549
| |
|
GSM1100489 | GPL570 |
|
Tubular Adenoma, sample 7
|
tubular adenoma
|
tissue: tubular adenoma
|
fap7
|
Sample_geo_accession | GSM1100489
| Sample_status | Public on Apr 14 2013
| Sample_submission_date | Mar 18 2013
| Sample_last_update_date | Apr 14 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 the 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 the One-Cycle cDNA synthesis Kit (Affymetrix) according to the 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 the manufacturer's protocol (Affymetrix).
| Sample_scan_protocol | Arrays were scanned with a GeneChip Scanner 3000 (Affymetrix) according to the 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/GSM1100nnn/GSM1100489/suppl/GSM1100489_EXT_429.CEL.gz
| Sample_series_id | GSE45270
| Sample_data_row_count | 34549
| |
|
GSM1100490 | GPL570 |
|
Serrated Adenoma, sample 1
|
serrated adenoma
|
tissue: serrated adenoma
|
serrated 10
|
Sample_geo_accession | GSM1100490
| Sample_status | Public on Apr 14 2013
| Sample_submission_date | Mar 18 2013
| Sample_last_update_date | Apr 14 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 the 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 the One-Cycle cDNA synthesis Kit (Affymetrix) according to the 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 the manufacturer's protocol (Affymetrix).
| Sample_scan_protocol | Arrays were scanned with a GeneChip Scanner 3000 (Affymetrix) according to the 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/GSM1100nnn/GSM1100490/suppl/GSM1100490_EXT_417.CEL.gz
| Sample_series_id | GSE45270
| Sample_data_row_count | 34549
| |
|
GSM1100491 | GPL570 |
|
Serrated Adenoma, sample 2
|
serrated adenoma
|
tissue: serrated adenoma
|
serrated 14
|
Sample_geo_accession | GSM1100491
| Sample_status | Public on Apr 14 2013
| Sample_submission_date | Mar 18 2013
| Sample_last_update_date | Apr 14 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 the 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 the One-Cycle cDNA synthesis Kit (Affymetrix) according to the 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 the manufacturer's protocol (Affymetrix).
| Sample_scan_protocol | Arrays were scanned with a GeneChip Scanner 3000 (Affymetrix) according to the 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/GSM1100nnn/GSM1100491/suppl/GSM1100491_EXT_418.CEL.gz
| Sample_series_id | GSE45270
| Sample_data_row_count | 34549
| |
|
GSM1100492 | GPL570 |
|
Serrated Adenoma, sample 3
|
serrated adenoma
|
tissue: serrated adenoma
|
serrated 15
|
Sample_geo_accession | GSM1100492
| Sample_status | Public on Apr 14 2013
| Sample_submission_date | Mar 18 2013
| Sample_last_update_date | Apr 14 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 the 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 the One-Cycle cDNA synthesis Kit (Affymetrix) according to the 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 the manufacturer's protocol (Affymetrix).
| Sample_scan_protocol | Arrays were scanned with a GeneChip Scanner 3000 (Affymetrix) according to the 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/GSM1100nnn/GSM1100492/suppl/GSM1100492_EXT_419.CEL.gz
| Sample_series_id | GSE45270
| Sample_data_row_count | 34549
| |
|
GSM1100493 | GPL570 |
|
Serrated Adenoma, sample 4
|
serrated adenoma
|
tissue: serrated adenoma
|
serrated 16
|
Sample_geo_accession | GSM1100493
| Sample_status | Public on Apr 14 2013
| Sample_submission_date | Mar 18 2013
| Sample_last_update_date | Apr 14 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 the 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 the One-Cycle cDNA synthesis Kit (Affymetrix) according to the 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 the manufacturer's protocol (Affymetrix).
| Sample_scan_protocol | Arrays were scanned with a GeneChip Scanner 3000 (Affymetrix) according to the 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/GSM1100nnn/GSM1100493/suppl/GSM1100493_EXT_420.CEL.gz
| Sample_series_id | GSE45270
| Sample_data_row_count | 34549
| |
|
GSM1100494 | GPL570 |
|
Serrated Adenoma, sample 5
|
serrated adenoma
|
tissue: serrated adenoma
|
serrated 11
|
Sample_geo_accession | GSM1100494
| Sample_status | Public on Apr 14 2013
| Sample_submission_date | Mar 18 2013
| Sample_last_update_date | Apr 14 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 the 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 the One-Cycle cDNA synthesis Kit (Affymetrix) according to the 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 the manufacturer's protocol (Affymetrix).
| Sample_scan_protocol | Arrays were scanned with a GeneChip Scanner 3000 (Affymetrix) according to the 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/GSM1100nnn/GSM1100494/suppl/GSM1100494_EXT_421.CEL.gz
| Sample_series_id | GSE45270
| Sample_data_row_count | 34549
| |
|
GSM1100495 | GPL570 |
|
Serrated Adenoma, sample 6
|
serrated adenoma
|
tissue: serrated adenoma
|
serrated 12
|
Sample_geo_accession | GSM1100495
| Sample_status | Public on Apr 14 2013
| Sample_submission_date | Mar 18 2013
| Sample_last_update_date | Apr 14 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 the 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 the One-Cycle cDNA synthesis Kit (Affymetrix) according to the 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 the manufacturer's protocol (Affymetrix).
| Sample_scan_protocol | Arrays were scanned with a GeneChip Scanner 3000 (Affymetrix) according to the 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/GSM1100nnn/GSM1100495/suppl/GSM1100495_EXT_422.CEL.gz
| Sample_series_id | GSE45270
| Sample_data_row_count | 34549
| |
|
|
|
Make groups for comparisons |
(2 groups will be compared at a time) |
|
Select GSMs and click on "Add groups" |
Enter the group name here: |
|
|
|