Search results for the GEO ID: GSE19238 |
(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 |
GSM476767 | GPL570 |
|
Sample1
|
subcutaneous adipose tissue
|
tissue: adbominal subcutaneous adipose tissue, collected via needle biopsy
genome/variation: del 16p11.2
disease status: obese
|
gene expression data from subcutaneous adipose tissue from an obese individual
|
Sample_geo_accession | GSM476767
| Sample_status | Public on Dec 02 2009
| Sample_submission_date | Dec 01 2009
| Sample_last_update_date | Dec 01 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 | Qiagen Lipid Tissue RNA extraction kit.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 3 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 Human U133 Plus 2.0 arrays. Arrays were washed and stained in the Affymetrix Fluidics Station 450.
| Sample_scan_protocol | After hybridisation (according to the Minimum Information About a Microarray Experiment guideline, the arrays were scanned using an Affymetrix confocal laser scanner (Affymetrix, GeneArray scanner GCS3000) and visualised using GeneChip Operating Software (GCOS, Affymetrix).
| Sample_data_processing | Gene expression levels were normalised using the Robust Multiarray Average (RMA) method.
| Sample_platform_id | GPL570
| Sample_contact_name | Johanna,Cecilia,Andersson
| Sample_contact_email | j.andersson@imperial.ac.uk
| Sample_contact_laboratory | Froguel
| Sample_contact_department | Division of Genetics of Common Disease
| Sample_contact_institute | Imperial College London
| Sample_contact_address | Burlington Danes Building, Hammersmith Hospital, Du Cane Road
| Sample_contact_city | London
| Sample_contact_zip/postal_code | W12 0NN
| Sample_contact_country | United Kingdom
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM476nnn/GSM476767/suppl/GSM476767.CEL.gz
| Sample_series_id | GSE19238
| Sample_data_row_count | 54675
| |
|
GSM476768 | GPL570 |
|
Sample2
|
subcutaneous adipose tissue
|
tissue: adbominal subcutaneous adipose tissue, collected via needle biopsy
genome/variation: del 16p11.2
disease status: obese
|
gene expression data from subcutaneous adipose tissue from an obese individual
|
Sample_geo_accession | GSM476768
| Sample_status | Public on Dec 02 2009
| Sample_submission_date | Dec 01 2009
| Sample_last_update_date | Dec 01 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 | Qiagen Lipid Tissue RNA extraction kit.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 3 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 Human U133 Plus 2.0 arrays. Arrays were washed and stained in the Affymetrix Fluidics Station 450.
| Sample_scan_protocol | After hybridisation (according to the Minimum Information About a Microarray Experiment guideline, the arrays were scanned using an Affymetrix confocal laser scanner (Affymetrix, GeneArray scanner GCS3000) and visualised using GeneChip Operating Software (GCOS, Affymetrix).
| Sample_data_processing | Gene expression levels were normalised using the Robust Multiarray Average (RMA) method.
| Sample_platform_id | GPL570
| Sample_contact_name | Johanna,Cecilia,Andersson
| Sample_contact_email | j.andersson@imperial.ac.uk
| Sample_contact_laboratory | Froguel
| Sample_contact_department | Division of Genetics of Common Disease
| Sample_contact_institute | Imperial College London
| Sample_contact_address | Burlington Danes Building, Hammersmith Hospital, Du Cane Road
| Sample_contact_city | London
| Sample_contact_zip/postal_code | W12 0NN
| Sample_contact_country | United Kingdom
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM476nnn/GSM476768/suppl/GSM476768.CEL.gz
| Sample_series_id | GSE19238
| 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 |
|
|