Search results for the GEO ID: GSE26393 |
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GSM ID | GPL ID |
Select for analysis |
Title |
Source name |
Description |
Characteristics |
GSM647870 | GPL1261 |
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JN_RG
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FACS sorted P4 early bulge stem cells from K14-RFP/Sox9-EGFP mice
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tissue: skin
strain: CD-1
genotype: K14-RFP/Sox9-EGFP
age: P4
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Gene expression data from FACS sorted P4 early bulge stem cells
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Sample_geo_accession | GSM647870
| Sample_status | Public on Jan 04 2011
| Sample_submission_date | Jan 03 2011
| Sample_last_update_date | Jan 04 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | Hair follicle cells were isolated from P4 Backskin of K14-RFP/Sox9-EGFP double transgenic mice as following: interfollicular epidermis sheet was pealed from hair follicle & dermis after dispase treatment. The hair follicle & dermis were first digested by collagenase (Sigma). Intact hair follicles were separated from dermal cells by low speed spinning (20g). The hair follicles were then digested by Trypsin and filtered by 40 µm cell strainers. The isolated hair follicle cells were FACS sorted. Dead cells and large differentiated cells were excluded based on DAPI and side scattering. Early bulge cells were gated as GFPHi,RFPHi. Non-bulge ORS cells were gated as GFP-, RFPHi.
| Sample_growth_protocol_ch1 | Standard mouse growth protocol
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | miRNeasy kit (Qiagen) 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 (Expression Analysis Technical Manual, 2001, Affymetrix).
| Sample_hyb_protocol | Labeled cRNA samples were hybridized to MOE 430 2.0 mouse expression arrays which were processed and analyzed according to standard Affymetrix protocols.
| Sample_scan_protocol | Standard Affymetrix protocol
| Sample_data_processing | The data were analyzed with Microarray Suite version 5.0 (MAS 5.0) using Affymetrix expression console default analysis settings
| Sample_platform_id | GPL1261
| Sample_contact_name | liang,,zhang
| Sample_contact_email | liangz@colorado.edu
| Sample_contact_institute | university of colorado at boulder
| Sample_contact_address | University of Colorado at Boulder, Han lab, Department of MCD Biology, Campus box 0347
| Sample_contact_city | Boulder
| Sample_contact_state | CO
| Sample_contact_zip/postal_code | 80309-0347
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM647nnn/GSM647870/suppl/GSM647870_JN_RG.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM647nnn/GSM647870/suppl/GSM647870_JN_RG.CHP.gz
| Sample_series_id | GSE26393
| Sample_series_id | GSE26396
| Sample_data_row_count | 45101
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GSM647871 | GPL1261 |
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JN_Rhi
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FACS sorted P4 non-bulge ORS cells from K14-RFP/Sox9-EGFP mice
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tissue: skin
strain: CD-1
genotype: K14-RFP/Sox9-EGFP
age: P4
|
Gene expression data from FACS sorted P4 non-bulge ORS cells
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Sample_geo_accession | GSM647871
| Sample_status | Public on Jan 04 2011
| Sample_submission_date | Jan 03 2011
| Sample_last_update_date | Jan 04 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | Hair follicle cells were isolated from P4 Backskin of K14-RFP/Sox9-EGFP double transgenic mice as following: interfollicular epidermis sheet was pealed from hair follicle & dermis after dispase treatment. The hair follicle & dermis were first digested by collagenase (Sigma). Intact hair follicles were separated from dermal cells by low speed spinning (20g). The hair follicles were then digested by Trypsin and filtered by 40 µm cell strainers. The isolated hair follicle cells were FACS sorted. Dead cells and large differentiated cells were excluded based on DAPI and side scattering. Early bulge cells were gated as GFPHi,RFPHi. Non-bulge ORS cells were gated as GFP-, RFPHi.
| Sample_growth_protocol_ch1 | Standard mouse growth protocol
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | miRNeasy kit (Qiagen) 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 (Expression Analysis Technical Manual, 2001, Affymetrix).
| Sample_hyb_protocol | Labeled cRNA samples were hybridized to MOE 430 2.0 mouse expression arrays which were processed and analyzed according to standard Affymetrix protocols.
| Sample_scan_protocol | Standard Affymetrix protocol
| Sample_data_processing | The data were analyzed with Microarray Suite version 5.0 (MAS 5.0) using Affymetrix expression console default analysis settings
| Sample_platform_id | GPL1261
| Sample_contact_name | liang,,zhang
| Sample_contact_email | liangz@colorado.edu
| Sample_contact_institute | university of colorado at boulder
| Sample_contact_address | University of Colorado at Boulder, Han lab, Department of MCD Biology, Campus box 0347
| Sample_contact_city | Boulder
| Sample_contact_state | CO
| Sample_contact_zip/postal_code | 80309-0347
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM647nnn/GSM647871/suppl/GSM647871_JN_RHi.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM647nnn/GSM647871/suppl/GSM647871_JN_RHi.CHP.gz
| Sample_series_id | GSE26393
| Sample_series_id | GSE26396
| Sample_data_row_count | 45101
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