Search results for the GEO ID: GSE27974 |
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GSM ID | GPL ID |
Select for analysis |
Title |
Source name |
Description |
Characteristics |
GSM692131 | GPL570 |
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5min HCMV
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cell
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cell type: foreskin fibroblasts
time of hcmv infection: 5 minutes
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5min
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Sample_geo_accession | GSM692131
| Sample_status | Public on Mar 15 2013
| Sample_submission_date | Mar 15 2011
| Sample_last_update_date | Mar 15 2013
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | The MOI 10 was used to infect cells for RNA extraction
| Sample_growth_protocol_ch1 | human foreskin fibroblasts were grownconfluence of ~80% when infected with HCMV Towne strain
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | RNA was purified using the RNeasy RNA purification kit (QIAGEN Inc. Valencia, CA) followed by DNase treatment to eliminate all traces of DNA, according to the manufacturer's recommendation
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol
| Sample_hyb_protocol | Following fragmentation, 15 ug of cRNA were hybridized following affy protocol
| Sample_scan_protocol | GeneChips were scanned in stanford affy central
| Sample_data_processing | The data were analyzed with R.2.10
| Sample_platform_id | GPL570
| Sample_contact_name | ANYOU,,WANG
| Sample_contact_email | anyouwang@mednet.ucla.edu
| Sample_contact_department | Human Genetics
| Sample_contact_institute | UCLA
| Sample_contact_address | Gonda BLDG
| Sample_contact_city | Los Angeles
| Sample_contact_state | CA
| Sample_contact_zip/postal_code | CA90095
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM692nnn/GSM692131/suppl/GSM692131.CEL.gz
| Sample_series_id | GSE27974
| Sample_data_row_count | 54675
| |
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GSM692132 | GPL570 |
|
25min HCMV
|
cell
|
cell type: foreskin fibroblasts
time of hcmv infection: 25 minutes
|
25min
|
Sample_geo_accession | GSM692132
| Sample_status | Public on Mar 15 2013
| Sample_submission_date | Mar 15 2011
| Sample_last_update_date | Mar 15 2013
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | The MOI 10 was used to infect cells for RNA extraction
| Sample_growth_protocol_ch1 | human foreskin fibroblasts were grownconfluence of ~80% when infected with HCMV Towne strain
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | RNA was purified using the RNeasy RNA purification kit (QIAGEN Inc. Valencia, CA) followed by DNase treatment to eliminate all traces of DNA, according to the manufacturer's recommendation
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol
| Sample_hyb_protocol | Following fragmentation, 15 ug of cRNA were hybridized following affy protocol
| Sample_scan_protocol | GeneChips were scanned in stanford affy central
| Sample_data_processing | The data were analyzed with R.2.10
| Sample_platform_id | GPL570
| Sample_contact_name | ANYOU,,WANG
| Sample_contact_email | anyouwang@mednet.ucla.edu
| Sample_contact_department | Human Genetics
| Sample_contact_institute | UCLA
| Sample_contact_address | Gonda BLDG
| Sample_contact_city | Los Angeles
| Sample_contact_state | CA
| Sample_contact_zip/postal_code | CA90095
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM692nnn/GSM692132/suppl/GSM692132.CEL.gz
| Sample_series_id | GSE27974
| Sample_data_row_count | 54675
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