Search results for the GEO ID: GSE7412 |
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|
GSM ID | GPL ID |
Select for analysis |
Title |
Source name |
Description |
Characteristics |
GSM179064 | GPL339 |
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SRF Wt. IgM+IgD+ (GBF0551)
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FACS sorted IgM+IgD+ cells
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genetic modification: no modification
tissue: spleen: FACS sorted IgM+IgD+ cells
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SRF Wt. IgM+IgD+ cells
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Sample_geo_accession | GSM179064
| Sample_status | Public on Jun 27 2007
| Sample_submission_date | Mar 30 2007
| Sample_last_update_date | Jun 27 2007
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_growth_protocol_ch1 | primary cells
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Rneasy
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 microg total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| Sample_hyb_protocol | Following fragmentation, 10 microg of cRNA were hybridized for 16 hr at conditions recommended by the manufacturer. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix GCS 3000.
| 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 150.
| Sample_platform_id | GPL339
| Sample_contact_name | Robert,,Geffers
| Sample_contact_email | robert.geffers@helmholtz-hzi.de
| Sample_contact_phone | +49 531-6181-3058
| Sample_contact_laboratory | Array Facility
| Sample_contact_department | Dep. Cell Biology
| Sample_contact_institute | HCI - Helmholtz Centre for Infection Research
| Sample_contact_address | Inhoffenstr. 7
| Sample_contact_city | Braunschweig
| Sample_contact_zip/postal_code | 38124
| Sample_contact_country | Germany
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM179nnn/GSM179064/suppl/GSM179064.CEL.gz
| Sample_series_id | GSE7412
| Sample_data_row_count | 22690
| |
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GSM179065 | GPL339 |
|
SRF Mut. IgM+IgD+ (GBF0552)
|
FACS sorted IgM+IgD+ cells
|
genetic modification: Cd19-cre mediated deletion of the SRF Gene
tissue: spleen: FACS sorted IgM+IgD+ cells
|
SRF Mut. IgM+IgD+ cells
|
Sample_geo_accession | GSM179065
| Sample_status | Public on Jun 27 2007
| Sample_submission_date | Mar 30 2007
| Sample_last_update_date | Jun 27 2007
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_growth_protocol_ch1 | primary cells
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Rneasy
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 microg total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| Sample_hyb_protocol | Following fragmentation, 10 microg of cRNA were hybridized for 16 hr at conditions recommended by the manufacturer. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix GCS 3000.
| 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 150.
| Sample_platform_id | GPL339
| Sample_contact_name | Robert,,Geffers
| Sample_contact_email | robert.geffers@helmholtz-hzi.de
| Sample_contact_phone | +49 531-6181-3058
| Sample_contact_laboratory | Array Facility
| Sample_contact_department | Dep. Cell Biology
| Sample_contact_institute | HCI - Helmholtz Centre for Infection Research
| Sample_contact_address | Inhoffenstr. 7
| Sample_contact_city | Braunschweig
| Sample_contact_zip/postal_code | 38124
| Sample_contact_country | Germany
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM179nnn/GSM179065/suppl/GSM179065.CEL.gz
| Sample_series_id | GSE7412
| Sample_data_row_count | 22690
| |
|
GSM179066 | GPL339 |
|
SRF Wt. IgM+IgD+ (GBF0610)
|
FACS sorted IgM+IgD+ cells
|
genetic modification: no modification
tissue: spleen: FACS sorted IgM+IgD+ cells
|
SRF Wt. IgM+IgD+ cells
|
Sample_geo_accession | GSM179066
| Sample_status | Public on Jun 27 2007
| Sample_submission_date | Mar 30 2007
| Sample_last_update_date | Jun 27 2007
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_growth_protocol_ch1 | primary cells
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Rneasy
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 microg total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| Sample_hyb_protocol | Following fragmentation, 10 microg of cRNA were hybridized for 16 hr at conditions recommended by the manufacturer. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix GCS 3000.
| 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 150.
| Sample_platform_id | GPL339
| Sample_contact_name | Robert,,Geffers
| Sample_contact_email | robert.geffers@helmholtz-hzi.de
| Sample_contact_phone | +49 531-6181-3058
| Sample_contact_laboratory | Array Facility
| Sample_contact_department | Dep. Cell Biology
| Sample_contact_institute | HCI - Helmholtz Centre for Infection Research
| Sample_contact_address | Inhoffenstr. 7
| Sample_contact_city | Braunschweig
| Sample_contact_zip/postal_code | 38124
| Sample_contact_country | Germany
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM179nnn/GSM179066/suppl/GSM179066.CEL.gz
| Sample_series_id | GSE7412
| Sample_data_row_count | 22690
| |
|
GSM179067 | GPL339 |
|
SRF Mut. IgM+IgD+ (GBF0611)
|
FACS sorted IgM+IgD+ cells
|
genetic modification: Cd19-cre mediated deletion of the SRF Gene
tissue: spleen: FACS sorted IgM+IgD+ cells
|
SRF Mut. IgM+IgD+ cells
|
Sample_geo_accession | GSM179067
| Sample_status | Public on Jun 27 2007
| Sample_submission_date | Mar 30 2007
| Sample_last_update_date | Jun 27 2007
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_growth_protocol_ch1 | primary cells
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Rneasy
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 microg total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| Sample_hyb_protocol | Following fragmentation, 10 microg of cRNA were hybridized for 16 hr at conditions recommended by the manufacturer. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix GCS 3000.
| 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 150.
| Sample_platform_id | GPL339
| Sample_contact_name | Robert,,Geffers
| Sample_contact_email | robert.geffers@helmholtz-hzi.de
| Sample_contact_phone | +49 531-6181-3058
| Sample_contact_laboratory | Array Facility
| Sample_contact_department | Dep. Cell Biology
| Sample_contact_institute | HCI - Helmholtz Centre for Infection Research
| Sample_contact_address | Inhoffenstr. 7
| Sample_contact_city | Braunschweig
| Sample_contact_zip/postal_code | 38124
| Sample_contact_country | Germany
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM179nnn/GSM179067/suppl/GSM179067.CEL.gz
| Sample_series_id | GSE7412
| Sample_data_row_count | 22690
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