Search results for the GEO ID: GSE28240  |
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|
GSM ID | GPL ID |
Select for analysis |
Title |
Source name |
Description |
Characteristics |
GSM699125 | GPL1261 |
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Endothelial SP-rep1
|
mouse CD31+CD45- side population
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tissue: endothelial cells from hindlimb
strain: C57BL/6
age: 8 weeks
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EC-SP (SP1)
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| Sample_geo_accession | GSM699125
| | Sample_status | Public on Mar 29 2012
| | Sample_submission_date | Mar 29 2011
| | Sample_last_update_date | Mar 29 2012
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Mus musculus
| | Sample_taxid_ch1 | 10090
| | Sample_treatment_protocol_ch1 | Hindlimb muscle were minced and dispersed with dispase and collagenase
| | Sample_growth_protocol_ch1 | Wild type mice were bred conventionally
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | RNA was extracted using an RNeasy Mini Kit (Qiagen)
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Biotinylated cRNA were prepared with Two-cycle Target Labeling Protocol according to the standard Affymetrix protocol from 10 ng total RNA
| | Sample_hyb_protocol | Following fragmentation, 15 ug of cRNA were hybridized for 16 hr on Mouse Genome 430 2.0 Array. GeneChips were washed and stained in the Fluidics Station 450.
| | Sample_scan_protocol | GeneChips were scanned using the GeneChip Scanner 3000.
| | Sample_data_processing | The data were analyzed with AGCC (Affymetrix GeneChip Command Console), Affymetrix expression console and GeneSpring GX 10.0.
| | Sample_platform_id | GPL1261
| | Sample_contact_name | Hisamichi,,Naito
| | Sample_contact_email | naitohi@biken.osaka-u.ac.jp
| | Sample_contact_phone | 81-6879-8312
| | Sample_contact_fax | 81-6879-8314
| | Sample_contact_department | Signal Transduction
| | Sample_contact_institute | The Research Institute for Microbial Diseases
| | Sample_contact_address | Yamada-oka 3-1
| | Sample_contact_city | Suita
| | Sample_contact_state | Osaka
| | Sample_contact_zip/postal_code | 5650871
| | Sample_contact_country | Japan
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM699nnn/GSM699125/suppl/GSM699125.CEL.gz
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM699nnn/GSM699125/suppl/GSM699125.CHP.gz
| | Sample_series_id | GSE28240
| | Sample_data_row_count | 45101
| | |
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GSM699126 | GPL1261 |
|
Endothelial SP-rep2
|
mouse CD31+CD45- side population
|
tissue: endothelial cells from hindlimb
strain: C57BL/6
age: 8 weeks
|
SP2
|
| Sample_geo_accession | GSM699126
| | Sample_status | Public on Mar 29 2012
| | Sample_submission_date | Mar 29 2011
| | Sample_last_update_date | Mar 29 2012
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Mus musculus
| | Sample_taxid_ch1 | 10090
| | Sample_treatment_protocol_ch1 | Hindlimb muscle were minced and dispersed with dispase and collagenase
| | Sample_growth_protocol_ch1 | Wild type mice were bred conventionally
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | RNA was extracted using an RNeasy Mini Kit (Qiagen)
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Biotinylated cRNA were prepared with Two-cycle Target Labeling Protocol according to the standard Affymetrix protocol from 10 ng total RNA
| | Sample_hyb_protocol | Following fragmentation, 15 ug of cRNA were hybridized for 16 hr on Mouse Genome 430 2.0 Array. GeneChips were washed and stained in the Fluidics Station 450.
| | Sample_scan_protocol | GeneChips were scanned using the GeneChip Scanner 3000.
| | Sample_data_processing | The data were analyzed with AGCC (Affymetrix GeneChip Command Console), Affymetrix expression console and GeneSpring GX 10.0.
| | Sample_platform_id | GPL1261
| | Sample_contact_name | Hisamichi,,Naito
| | Sample_contact_email | naitohi@biken.osaka-u.ac.jp
| | Sample_contact_phone | 81-6879-8312
| | Sample_contact_fax | 81-6879-8314
| | Sample_contact_department | Signal Transduction
| | Sample_contact_institute | The Research Institute for Microbial Diseases
| | Sample_contact_address | Yamada-oka 3-1
| | Sample_contact_city | Suita
| | Sample_contact_state | Osaka
| | Sample_contact_zip/postal_code | 5650871
| | Sample_contact_country | Japan
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM699nnn/GSM699126/suppl/GSM699126.CEL.gz
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM699nnn/GSM699126/suppl/GSM699126.CHP.gz
| | Sample_series_id | GSE28240
| | Sample_data_row_count | 45101
| | |
|
GSM699127 | GPL1261 |
|
Endothelial MP-rep1
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mouse CD31+CD45- main population
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tissue: endothelial cells from hindlimb
strain: C57BL/6
age: 8 weeks
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EC-MP (MP1)
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| Sample_geo_accession | GSM699127
| | Sample_status | Public on Mar 29 2012
| | Sample_submission_date | Mar 29 2011
| | Sample_last_update_date | Mar 29 2012
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Mus musculus
| | Sample_taxid_ch1 | 10090
| | Sample_treatment_protocol_ch1 | Hindlimb muscle were minced and dispersed with dispase and collagenase
| | Sample_growth_protocol_ch1 | Wild type mice were bred conventionally
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | RNA was extracted using an RNeasy Mini Kit (Qiagen)
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Biotinylated cRNA were prepared with Two-cycle Target Labeling Protocol according to the standard Affymetrix protocol from 10 ng total RNA
| | Sample_hyb_protocol | Following fragmentation, 15 ug of cRNA were hybridized for 16 hr on Mouse Genome 430 2.0 Array. GeneChips were washed and stained in the Fluidics Station 450.
| | Sample_scan_protocol | GeneChips were scanned using the GeneChip Scanner 3000.
| | Sample_data_processing | The data were analyzed with AGCC (Affymetrix GeneChip Command Console), Affymetrix expression console and GeneSpring GX 10.0.
| | Sample_platform_id | GPL1261
| | Sample_contact_name | Hisamichi,,Naito
| | Sample_contact_email | naitohi@biken.osaka-u.ac.jp
| | Sample_contact_phone | 81-6879-8312
| | Sample_contact_fax | 81-6879-8314
| | Sample_contact_department | Signal Transduction
| | Sample_contact_institute | The Research Institute for Microbial Diseases
| | Sample_contact_address | Yamada-oka 3-1
| | Sample_contact_city | Suita
| | Sample_contact_state | Osaka
| | Sample_contact_zip/postal_code | 5650871
| | Sample_contact_country | Japan
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM699nnn/GSM699127/suppl/GSM699127.CEL.gz
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM699nnn/GSM699127/suppl/GSM699127.CHP.gz
| | Sample_series_id | GSE28240
| | Sample_data_row_count | 45101
| | |
|
GSM699128 | GPL1261 |
|
Endothelial MP-rep2
|
mouse CD31+CD45- main population
|
tissue: endothelial cells from hindlimb
strain: C57BL/6
age: 8 weeks
|
MP2
|
| Sample_geo_accession | GSM699128
| | Sample_status | Public on Mar 29 2012
| | Sample_submission_date | Mar 29 2011
| | Sample_last_update_date | Mar 29 2012
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Mus musculus
| | Sample_taxid_ch1 | 10090
| | Sample_treatment_protocol_ch1 | Hindlimb muscle were minced and dispersed with dispase and collagenase
| | Sample_growth_protocol_ch1 | Wild type mice were bred conventionally
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | RNA was extracted using an RNeasy Mini Kit (Qiagen)
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Biotinylated cRNA were prepared with Two-cycle Target Labeling Protocol according to the standard Affymetrix protocol from 10 ng total RNA
| | Sample_hyb_protocol | Following fragmentation, 15 ug of cRNA were hybridized for 16 hr on Mouse Genome 430 2.0 Array. GeneChips were washed and stained in the Fluidics Station 450.
| | Sample_scan_protocol | GeneChips were scanned using the GeneChip Scanner 3000.
| | Sample_data_processing | The data were analyzed with AGCC (Affymetrix GeneChip Command Console), Affymetrix expression console and GeneSpring GX 10.0.
| | Sample_platform_id | GPL1261
| | Sample_contact_name | Hisamichi,,Naito
| | Sample_contact_email | naitohi@biken.osaka-u.ac.jp
| | Sample_contact_phone | 81-6879-8312
| | Sample_contact_fax | 81-6879-8314
| | Sample_contact_department | Signal Transduction
| | Sample_contact_institute | The Research Institute for Microbial Diseases
| | Sample_contact_address | Yamada-oka 3-1
| | Sample_contact_city | Suita
| | Sample_contact_state | Osaka
| | Sample_contact_zip/postal_code | 5650871
| | Sample_contact_country | Japan
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM699nnn/GSM699128/suppl/GSM699128.CEL.gz
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM699nnn/GSM699128/suppl/GSM699128.CHP.gz
| | Sample_series_id | GSE28240
| | Sample_data_row_count | 45101
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