Search results for the GEO ID: GSE15537 |
(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 |
GSM389321 | GPL570 |
|
CRL-2072(1)
|
normal skin fibroblasts
|
tissue: skin
|
Gene expression of normal skin fibroblasts
|
Sample_geo_accession | GSM389321
| Sample_status | Public on Oct 06 2009
| Sample_submission_date | Apr 03 2009
| Sample_last_update_date | Oct 06 2009
| 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 | RNeasy mini spin columns (Qiagen) were used according to the manufacturer's instructions.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 5 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| Sample_hyb_protocol | Following fragmentation, 15 ug of cRNA were hybridized for 16 hr at 45C on GeneChip® Human Genome U133 Plus 2.0 Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 450.
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix GeneChip Scanner GCS3000 7G.
| Sample_data_processing | The data were analyzed with Microarray Suite version 5.0 (MAS 5.0) using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 500.
| Sample_platform_id | GPL570
| Sample_contact_name | Chia-Huey,,Ooi
| Sample_contact_email | chia-huey.ooi@roche.com
| Sample_contact_phone | +49 8856 60 19703
| Sample_contact_institute | Roche Diagnostics GmbH
| Sample_contact_address | Nonnenwald 2
| Sample_contact_city | Penzberg
| Sample_contact_zip/postal_code | 82377
| Sample_contact_country | Germany
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM389nnn/GSM389321/suppl/GSM389321.CEL.gz
| Sample_series_id | GSE15460
| Sample_series_id | GSE15537
| Sample_data_row_count | 54675
| |
|
GSM389322 | GPL570 |
|
CRL-2072(2)
|
normal skin fibroblasts
|
tissue: skin
|
Gene expression of normal skin fibroblasts
|
Sample_geo_accession | GSM389322
| Sample_status | Public on Oct 06 2009
| Sample_submission_date | Apr 03 2009
| Sample_last_update_date | Oct 06 2009
| 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 | RNeasy mini spin columns (Qiagen) were used according to the manufacturer's instructions.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 5 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| Sample_hyb_protocol | Following fragmentation, 15 ug of cRNA were hybridized for 16 hr at 45C on GeneChip® Human Genome U133 Plus 2.0 Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 450.
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix GeneChip Scanner GCS3000 7G.
| Sample_data_processing | The data were analyzed with Microarray Suite version 5.0 (MAS 5.0) using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 500.
| Sample_platform_id | GPL570
| Sample_contact_name | Chia-Huey,,Ooi
| Sample_contact_email | chia-huey.ooi@roche.com
| Sample_contact_phone | +49 8856 60 19703
| Sample_contact_institute | Roche Diagnostics GmbH
| Sample_contact_address | Nonnenwald 2
| Sample_contact_city | Penzberg
| Sample_contact_zip/postal_code | 82377
| Sample_contact_country | Germany
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM389nnn/GSM389322/suppl/GSM389322.CEL.gz
| Sample_series_id | GSE15460
| Sample_series_id | GSE15537
| Sample_data_row_count | 54675
| |
|
GSM389323 | GPL570 |
|
CRL-2072(3)
|
normal skin fibroblasts
|
tissue: skin
|
Gene expression of normal skin fibroblasts
|
Sample_geo_accession | GSM389323
| Sample_status | Public on Oct 06 2009
| Sample_submission_date | Apr 03 2009
| Sample_last_update_date | Oct 06 2009
| 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 | RNeasy mini spin columns (Qiagen) were used according to the manufacturer's instructions.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 5 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| Sample_hyb_protocol | Following fragmentation, 15 ug of cRNA were hybridized for 16 hr at 45C on GeneChip® Human Genome U133 Plus 2.0 Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 450.
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix GeneChip Scanner GCS3000 7G.
| Sample_data_processing | The data were analyzed with Microarray Suite version 5.0 (MAS 5.0) using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 500.
| Sample_platform_id | GPL570
| Sample_contact_name | Chia-Huey,,Ooi
| Sample_contact_email | chia-huey.ooi@roche.com
| Sample_contact_phone | +49 8856 60 19703
| Sample_contact_institute | Roche Diagnostics GmbH
| Sample_contact_address | Nonnenwald 2
| Sample_contact_city | Penzberg
| Sample_contact_zip/postal_code | 82377
| Sample_contact_country | Germany
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM389nnn/GSM389323/suppl/GSM389323.CEL.gz
| Sample_series_id | GSE15460
| Sample_series_id | GSE15537
| Sample_data_row_count | 54675
| |
|
|
|
Make groups for comparisons |
(2 groups will be compared at a time) |
|
Select GSMs and click on "Add groups" |
Enter the group name here: |
|
|
|
Select expression type |
Transcripts profile based on; |
A. Differential status (Up/Down regulation) |
|
|
Regulation type |
|
Fold change |
|
p-value |
|
|
|
B. Absolute calls (Transcribed/Not-detected) |
|
|
Derive calls within/across groups |
Within groups |
|
|
Detection status |
|
Percentage detection |
|
|
Across groups |
|
|
Detection status |
First group: |
- |
Second group:
|
Percentage detection |
First group: |
- |
Second group:
|
|
|
|
Filter results by number of probes |
|
|