Search results for the GEO ID: GSE31028 |
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|
GSM ID | GPL ID |
Select for analysis |
Title |
Source name |
Description |
Characteristics |
GSM768826 | GPL1261 |
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Quiescent hair follicle stem cells, rep1
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Mouse back skins, qHF-SCs
|
strain: CD-1
tissue: back skin
cell type: quiescent hair follicle stem cells
gender: female
age: P52-60
sorting markers: integrin α6, CD34
|
qHF-SC-1
Gene expression data from quiescent hair follicle stem cells.
|
Sample_geo_accession | GSM768826
| Sample_status | Public on Sep 02 2011
| Sample_submission_date | Jul 28 2011
| Sample_last_update_date | Jun 07 2012
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | No treatment.
| Sample_growth_protocol_ch1 | HF-SCs and HF-TACs were FACS-purified from the back skins of mice at the indicated ages.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Trizol extraction of total RNA was performed 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 2 ug total RNA.
| Sample_hyb_protocol | Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on a GeneChip Mouse 430 2.0 Genome Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 450.
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix 3000 7G Scanner.
| Sample_data_processing | The data were analyzed with the RMA method using Gene Pattern analysis settings and median scaling as the normalization method.
| Sample_platform_id | GPL1261
| Sample_contact_name | Wen-Hui,,Lien
| Sample_contact_email | wlien@rockefeller.edu
| Sample_contact_phone | 212-327-7482
| Sample_contact_laboratory | Elaine Fuchs
| Sample_contact_department | Mammalian cell biology and development
| Sample_contact_institute | The Rockefeller Unoversity
| Sample_contact_address | 1230 York Ave Box#300
| Sample_contact_city | New York
| Sample_contact_state | NY
| Sample_contact_zip/postal_code | 10065
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM768nnn/GSM768826/suppl/GSM768826.CEL.gz
| Sample_relation | Reanalyzed by: GSE38557
| Sample_series_id | GSE31028
| Sample_data_row_count | 45101
| |
|
GSM768827 | GPL1261 |
|
Quiescent hair follicle stem cells, rep2
|
Mouse back skins, qHF-SCs
|
strain: CD-1
tissue: back skin
cell type: quiescent hair follicle stem cells
gender: female
age: P52-60
sorting markers: integrin α6, CD34
|
qHF-SC-2
Gene expression data from quiescent hair follicle stem cells.
|
Sample_geo_accession | GSM768827
| Sample_status | Public on Sep 02 2011
| Sample_submission_date | Jul 28 2011
| Sample_last_update_date | Jun 07 2012
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | No treatment.
| Sample_growth_protocol_ch1 | HF-SCs and HF-TACs were FACS-purified from the back skins of mice at the indicated ages.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Trizol extraction of total RNA was performed 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 2 ug total RNA.
| Sample_hyb_protocol | Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on a GeneChip Mouse 430 2.0 Genome Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 450.
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix 3000 7G Scanner.
| Sample_data_processing | The data were analyzed with the RMA method using Gene Pattern analysis settings and median scaling as the normalization method.
| Sample_platform_id | GPL1261
| Sample_contact_name | Wen-Hui,,Lien
| Sample_contact_email | wlien@rockefeller.edu
| Sample_contact_phone | 212-327-7482
| Sample_contact_laboratory | Elaine Fuchs
| Sample_contact_department | Mammalian cell biology and development
| Sample_contact_institute | The Rockefeller Unoversity
| Sample_contact_address | 1230 York Ave Box#300
| Sample_contact_city | New York
| Sample_contact_state | NY
| Sample_contact_zip/postal_code | 10065
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM768nnn/GSM768827/suppl/GSM768827.CEL.gz
| Sample_relation | Reanalyzed by: GSE38557
| Sample_series_id | GSE31028
| Sample_data_row_count | 45101
| |
|
GSM768828 | GPL1261 |
|
Activated hair follicle stem cells, rep1
|
Mouse back skins, aHF-SCs
|
strain: CD-1
tissue: back skin
cell type: activated hair follicle stem cells
gender: female
age: P28-30
sorting markers: GFP, integrin α6, CD34
|
aHF-SC-1
Gene expression data from activated hair follicle stem cells.
|
Sample_geo_accession | GSM768828
| Sample_status | Public on Sep 02 2011
| Sample_submission_date | Jul 28 2011
| Sample_last_update_date | Jun 07 2012
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | No treatment.
| Sample_growth_protocol_ch1 | HF-SCs and HF-TACs were FACS-purified from the back skins of mice at the indicated ages.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Trizol extraction of total RNA was performed 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 2 ug total RNA.
| Sample_hyb_protocol | Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on a GeneChip Mouse 430 2.0 Genome Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 450.
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix 3000 7G Scanner.
| Sample_data_processing | The data were analyzed with the RMA method using Gene Pattern analysis settings and median scaling as the normalization method.
| Sample_platform_id | GPL1261
| Sample_contact_name | Wen-Hui,,Lien
| Sample_contact_email | wlien@rockefeller.edu
| Sample_contact_phone | 212-327-7482
| Sample_contact_laboratory | Elaine Fuchs
| Sample_contact_department | Mammalian cell biology and development
| Sample_contact_institute | The Rockefeller Unoversity
| Sample_contact_address | 1230 York Ave Box#300
| Sample_contact_city | New York
| Sample_contact_state | NY
| Sample_contact_zip/postal_code | 10065
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM768nnn/GSM768828/suppl/GSM768828.CEL.gz
| Sample_relation | Reanalyzed by: GSE38557
| Sample_series_id | GSE31028
| Sample_data_row_count | 45101
| |
|
GSM768829 | GPL1261 |
|
Activated hair follicle stem cells, rep2
|
Mouse back skins, aHF-SCs
|
strain: CD-1
tissue: back skin
cell type: activated hair follicle stem cells
gender: female
age: P28-30
sorting markers: GFP, integrin α6, CD34
|
aHF-SC-2
Gene expression data from activated hair follicle stem cells.
|
Sample_geo_accession | GSM768829
| Sample_status | Public on Sep 02 2011
| Sample_submission_date | Jul 28 2011
| Sample_last_update_date | Jun 07 2012
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | No treatment.
| Sample_growth_protocol_ch1 | HF-SCs and HF-TACs were FACS-purified from the back skins of mice at the indicated ages.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Trizol extraction of total RNA was performed 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 2 ug total RNA.
| Sample_hyb_protocol | Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on a GeneChip Mouse 430 2.0 Genome Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 450.
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix 3000 7G Scanner.
| Sample_data_processing | The data were analyzed with the RMA method using Gene Pattern analysis settings and median scaling as the normalization method.
| Sample_platform_id | GPL1261
| Sample_contact_name | Wen-Hui,,Lien
| Sample_contact_email | wlien@rockefeller.edu
| Sample_contact_phone | 212-327-7482
| Sample_contact_laboratory | Elaine Fuchs
| Sample_contact_department | Mammalian cell biology and development
| Sample_contact_institute | The Rockefeller Unoversity
| Sample_contact_address | 1230 York Ave Box#300
| Sample_contact_city | New York
| Sample_contact_state | NY
| Sample_contact_zip/postal_code | 10065
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM768nnn/GSM768829/suppl/GSM768829.CEL.gz
| Sample_relation | Reanalyzed by: GSE38557
| Sample_series_id | GSE31028
| Sample_data_row_count | 45101
| |
|
GSM768830 | GPL1261 |
|
Transient-amplifying matrix cells, rep1
|
Mouse back skins, HF-TACs
|
strain: CD-1
tissue: back skin
cell type: transient-amplifying matrix cells
gender: female
age: P28-30
sorting markers: GFP, integrin α6, ephrinB1
|
HF-TAC-1
Gene expression data from transient-amplifying progenitors.
|
Sample_geo_accession | GSM768830
| Sample_status | Public on Sep 02 2011
| Sample_submission_date | Jul 28 2011
| Sample_last_update_date | Jun 07 2012
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | No treatment.
| Sample_growth_protocol_ch1 | HF-SCs and HF-TACs were FACS-purified from the back skins of mice at the indicated ages.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Trizol extraction of total RNA was performed 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 2 ug total RNA.
| Sample_hyb_protocol | Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on a GeneChip Mouse 430 2.0 Genome Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 450.
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix 3000 7G Scanner.
| Sample_data_processing | The data were analyzed with the RMA method using Gene Pattern analysis settings and median scaling as the normalization method.
| Sample_platform_id | GPL1261
| Sample_contact_name | Wen-Hui,,Lien
| Sample_contact_email | wlien@rockefeller.edu
| Sample_contact_phone | 212-327-7482
| Sample_contact_laboratory | Elaine Fuchs
| Sample_contact_department | Mammalian cell biology and development
| Sample_contact_institute | The Rockefeller Unoversity
| Sample_contact_address | 1230 York Ave Box#300
| Sample_contact_city | New York
| Sample_contact_state | NY
| Sample_contact_zip/postal_code | 10065
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM768nnn/GSM768830/suppl/GSM768830.CEL.gz
| Sample_relation | Reanalyzed by: GSE38557
| Sample_series_id | GSE31028
| Sample_data_row_count | 45101
| |
|
GSM768831 | GPL1261 |
|
Transient-amplifying matrix cells, rep2
|
Mouse back skins, HF-TACs
|
strain: CD-1
tissue: back skin
cell type: transient-amplifying matrix cells
gender: female
age: P28-30
sorting markers: GFP, integrin α6, ephrinB1
|
HF-TAC-2
Gene expression data from transient-amplifying progenitors.
|
Sample_geo_accession | GSM768831
| Sample_status | Public on Sep 02 2011
| Sample_submission_date | Jul 28 2011
| Sample_last_update_date | Jun 07 2012
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | No treatment.
| Sample_growth_protocol_ch1 | HF-SCs and HF-TACs were FACS-purified from the back skins of mice at the indicated ages.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Trizol extraction of total RNA was performed 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 2 ug total RNA.
| Sample_hyb_protocol | Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on a GeneChip Mouse 430 2.0 Genome Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 450.
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix 3000 7G Scanner.
| Sample_data_processing | The data were analyzed with the RMA method using Gene Pattern analysis settings and median scaling as the normalization method.
| Sample_platform_id | GPL1261
| Sample_contact_name | Wen-Hui,,Lien
| Sample_contact_email | wlien@rockefeller.edu
| Sample_contact_phone | 212-327-7482
| Sample_contact_laboratory | Elaine Fuchs
| Sample_contact_department | Mammalian cell biology and development
| Sample_contact_institute | The Rockefeller Unoversity
| Sample_contact_address | 1230 York Ave Box#300
| Sample_contact_city | New York
| Sample_contact_state | NY
| Sample_contact_zip/postal_code | 10065
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM768nnn/GSM768831/suppl/GSM768831.CEL.gz
| Sample_relation | Reanalyzed by: GSE38557
| Sample_series_id | GSE31028
| Sample_data_row_count | 45101
| |
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