Search results for the GEO ID: GSE30012 |
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|
GSM ID | GPL ID |
Select for analysis |
Title |
Source name |
Description |
Characteristics |
GSM742803 | GPL1261 |
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Mouse Embryonic Stem Cells Control replicate 1
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Dicerflox/flox wild-type embryonic stem cells transfected with GFP
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genotype/variation: wild type (Dicer)
cell type: embryonic stem cells
transfection: GFP
|
Gene expression data from mouse embryoic stem cells with intact Dicer genes
|
Sample_geo_accession | GSM742803
| Sample_status | Public on Jun 18 2011
| Sample_submission_date | Jun 15 2011
| Sample_last_update_date | Jun 18 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | RNA was isolated 5 days following transfection of Dicerflox/flox wild-type cells with either GFP alone or GFP and Cre recombinase.
| Sample_growth_protocol_ch1 | ES cells were grown on gelatin in DMEM (GIBCO), 15% fetal calf serum (FCS, Hyclone), and 250 U LIF/ml (Y Marahrens, B Panning, J Dausman, W Strauss and R Jaenisch, Xist-deficient mice are defective in dosage compensation but not spermatogenesis, Genes Dev. 11 (1997), pp. 156–166) or 1000 U/ml when addressing the effect of Xist on undifferentiated ES cells.
| 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 5 ug total RNA according to the Affymetrix Expression Analysis Technical Manual.
| Sample_hyb_protocol | Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on Affymetrix Mouse Genome Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
| Sample_scan_protocol | GeneChips were scanned using the GeneChip Scanner 3000.
| Sample_data_processing | R version 2.11.1 (x86_64-pc-linux-gnu), affyPLM_1.24.1, preprocessCore_1.10.0, gcrma_2.20.0, affy_1.26.1, Biobase_2.8.0
| Sample_platform_id | GPL1261
| Sample_contact_name | Charles,Arthur,Whittaker
| Sample_contact_email | charliew@mit.edu
| Sample_contact_institute | Koch Institute
| Sample_contact_address | 77 Mass Ave 76-189
| Sample_contact_city | Cambridge
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02152
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM742nnn/GSM742803/suppl/GSM742803_CTRL1.CEL.gz
| Sample_series_id | GSE30012
| Sample_data_row_count | 45037
| |
|
GSM742804 | GPL1261 |
|
Mouse Embryonic Stem Cells Control replicate 2
|
Dicerflox/flox wild-type embryonic stem cells transfected with GFP
|
genotype/variation: wild type (Dicer)
cell type: embryonic stem cells
transfection: GFP
|
Gene expression data from mouse embryoic stem cells with intact Dicer genes
|
Sample_geo_accession | GSM742804
| Sample_status | Public on Jun 18 2011
| Sample_submission_date | Jun 15 2011
| Sample_last_update_date | Jun 18 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | RNA was isolated 5 days following transfection of Dicerflox/flox wild-type cells with either GFP alone or GFP and Cre recombinase.
| Sample_growth_protocol_ch1 | ES cells were grown on gelatin in DMEM (GIBCO), 15% fetal calf serum (FCS, Hyclone), and 250 U LIF/ml (Y Marahrens, B Panning, J Dausman, W Strauss and R Jaenisch, Xist-deficient mice are defective in dosage compensation but not spermatogenesis, Genes Dev. 11 (1997), pp. 156–166) or 1000 U/ml when addressing the effect of Xist on undifferentiated ES cells.
| 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 5 ug total RNA according to the Affymetrix Expression Analysis Technical Manual.
| Sample_hyb_protocol | Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on Affymetrix Mouse Genome Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
| Sample_scan_protocol | GeneChips were scanned using the GeneChip Scanner 3000.
| Sample_data_processing | R version 2.11.1 (x86_64-pc-linux-gnu), affyPLM_1.24.1, preprocessCore_1.10.0, gcrma_2.20.0, affy_1.26.1, Biobase_2.8.0
| Sample_platform_id | GPL1261
| Sample_contact_name | Charles,Arthur,Whittaker
| Sample_contact_email | charliew@mit.edu
| Sample_contact_institute | Koch Institute
| Sample_contact_address | 77 Mass Ave 76-189
| Sample_contact_city | Cambridge
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02152
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM742nnn/GSM742804/suppl/GSM742804_CTRL2.CEL.gz
| Sample_series_id | GSE30012
| Sample_data_row_count | 45037
| |
|
GSM742805 | GPL1261 |
|
Mouse Embryonic Stem Cells Control replicate 3
|
Dicerflox/flox wild-type embryonic stem cells transfected with GFP
|
genotype/variation: wild type (Dicer)
cell type: embryonic stem cells
transfection: GFP
|
Gene expression data from mouse embryoic stem cells with intact Dicer genes
|
Sample_geo_accession | GSM742805
| Sample_status | Public on Jun 18 2011
| Sample_submission_date | Jun 15 2011
| Sample_last_update_date | Jun 18 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | RNA was isolated 5 days following transfection of Dicerflox/flox wild-type cells with either GFP alone or GFP and Cre recombinase.
| Sample_growth_protocol_ch1 | ES cells were grown on gelatin in DMEM (GIBCO), 15% fetal calf serum (FCS, Hyclone), and 250 U LIF/ml (Y Marahrens, B Panning, J Dausman, W Strauss and R Jaenisch, Xist-deficient mice are defective in dosage compensation but not spermatogenesis, Genes Dev. 11 (1997), pp. 156–166) or 1000 U/ml when addressing the effect of Xist on undifferentiated ES cells.
| 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 5 ug total RNA according to the Affymetrix Expression Analysis Technical Manual.
| Sample_hyb_protocol | Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on Affymetrix Mouse Genome Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
| Sample_scan_protocol | GeneChips were scanned using the GeneChip Scanner 3000.
| Sample_data_processing | R version 2.11.1 (x86_64-pc-linux-gnu), affyPLM_1.24.1, preprocessCore_1.10.0, gcrma_2.20.0, affy_1.26.1, Biobase_2.8.0
| Sample_platform_id | GPL1261
| Sample_contact_name | Charles,Arthur,Whittaker
| Sample_contact_email | charliew@mit.edu
| Sample_contact_institute | Koch Institute
| Sample_contact_address | 77 Mass Ave 76-189
| Sample_contact_city | Cambridge
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02152
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM742nnn/GSM742805/suppl/GSM742805_CTRL3.CEL.gz
| Sample_series_id | GSE30012
| Sample_data_row_count | 45037
| |
|
GSM742806 | GPL1261 |
|
Mouse Embryonic Stem Cells Dicer Null - replicate 1
|
Dicerflox/flox wild-type embryonic stem cells transfected with GFP and Cre Recombinase
|
genotype/variation: Dicer Null (Cre)
cell type: embryonic stem cells
transfection: GFP+Cre
|
Gene expression data from mouse embryoic stem cells following acute Dicer deletion
|
Sample_geo_accession | GSM742806
| Sample_status | Public on Jun 18 2011
| Sample_submission_date | Jun 15 2011
| Sample_last_update_date | Jun 18 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | RNA was isolated 5 days following transfection of Dicerflox/flox wild-type cells with either GFP alone or GFP and Cre recombinase.
| Sample_growth_protocol_ch1 | ES cells were grown on gelatin in DMEM (GIBCO), 15% fetal calf serum (FCS, Hyclone), and 250 U LIF/ml (Y Marahrens, B Panning, J Dausman, W Strauss and R Jaenisch, Xist-deficient mice are defective in dosage compensation but not spermatogenesis, Genes Dev. 11 (1997), pp. 156–166) or 1000 U/ml when addressing the effect of Xist on undifferentiated ES cells.
| 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 5 ug total RNA according to the Affymetrix Expression Analysis Technical Manual.
| Sample_hyb_protocol | Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on Affymetrix Mouse Genome Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
| Sample_scan_protocol | GeneChips were scanned using the GeneChip Scanner 3000.
| Sample_data_processing | R version 2.11.1 (x86_64-pc-linux-gnu), affyPLM_1.24.1, preprocessCore_1.10.0, gcrma_2.20.0, affy_1.26.1, Biobase_2.8.0
| Sample_platform_id | GPL1261
| Sample_contact_name | Charles,Arthur,Whittaker
| Sample_contact_email | charliew@mit.edu
| Sample_contact_institute | Koch Institute
| Sample_contact_address | 77 Mass Ave 76-189
| Sample_contact_city | Cambridge
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02152
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM742nnn/GSM742806/suppl/GSM742806_CRE1.CEL.gz
| Sample_series_id | GSE30012
| Sample_data_row_count | 45037
| |
|
GSM742807 | GPL1261 |
|
Mouse Embryonic Stem Cells Dicer Null - replicate 2
|
Dicerflox/flox wild-type embryonic stem cells transfected with GFP and Cre Recombinase
|
genotype/variation: Dicer Null (Cre)
cell type: embryonic stem cells
transfection: GFP+Cre
|
Gene expression data from mouse embryoic stem cells following acute Dicer deletion
|
Sample_geo_accession | GSM742807
| Sample_status | Public on Jun 18 2011
| Sample_submission_date | Jun 15 2011
| Sample_last_update_date | Jun 18 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | RNA was isolated 5 days following transfection of Dicerflox/flox wild-type cells with either GFP alone or GFP and Cre recombinase.
| Sample_growth_protocol_ch1 | ES cells were grown on gelatin in DMEM (GIBCO), 15% fetal calf serum (FCS, Hyclone), and 250 U LIF/ml (Y Marahrens, B Panning, J Dausman, W Strauss and R Jaenisch, Xist-deficient mice are defective in dosage compensation but not spermatogenesis, Genes Dev. 11 (1997), pp. 156–166) or 1000 U/ml when addressing the effect of Xist on undifferentiated ES cells.
| 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 5 ug total RNA according to the Affymetrix Expression Analysis Technical Manual.
| Sample_hyb_protocol | Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on Affymetrix Mouse Genome Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
| Sample_scan_protocol | GeneChips were scanned using the GeneChip Scanner 3000.
| Sample_data_processing | R version 2.11.1 (x86_64-pc-linux-gnu), affyPLM_1.24.1, preprocessCore_1.10.0, gcrma_2.20.0, affy_1.26.1, Biobase_2.8.0
| Sample_platform_id | GPL1261
| Sample_contact_name | Charles,Arthur,Whittaker
| Sample_contact_email | charliew@mit.edu
| Sample_contact_institute | Koch Institute
| Sample_contact_address | 77 Mass Ave 76-189
| Sample_contact_city | Cambridge
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02152
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM742nnn/GSM742807/suppl/GSM742807_CRE2.CEL.gz
| Sample_series_id | GSE30012
| Sample_data_row_count | 45037
| |
|
GSM742808 | GPL1261 |
|
Mouse Embryonic Stem Cells Dicer Null - replicate 3
|
Dicerflox/flox wild-type embryonic stem cells transfected with GFP and Cre Recombinase
|
genotype/variation: Dicer Null (Cre)
cell type: embryonic stem cells
transfection: GFP+Cre
|
Gene expression data from mouse embryoic stem cells following acute Dicer deletion
|
Sample_geo_accession | GSM742808
| Sample_status | Public on Jun 18 2011
| Sample_submission_date | Jun 15 2011
| Sample_last_update_date | Jun 18 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | RNA was isolated 5 days following transfection of Dicerflox/flox wild-type cells with either GFP alone or GFP and Cre recombinase.
| Sample_growth_protocol_ch1 | ES cells were grown on gelatin in DMEM (GIBCO), 15% fetal calf serum (FCS, Hyclone), and 250 U LIF/ml (Y Marahrens, B Panning, J Dausman, W Strauss and R Jaenisch, Xist-deficient mice are defective in dosage compensation but not spermatogenesis, Genes Dev. 11 (1997), pp. 156–166) or 1000 U/ml when addressing the effect of Xist on undifferentiated ES cells.
| 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 5 ug total RNA according to the Affymetrix Expression Analysis Technical Manual.
| Sample_hyb_protocol | Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on Affymetrix Mouse Genome Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
| Sample_scan_protocol | GeneChips were scanned using the GeneChip Scanner 3000.
| Sample_data_processing | R version 2.11.1 (x86_64-pc-linux-gnu), affyPLM_1.24.1, preprocessCore_1.10.0, gcrma_2.20.0, affy_1.26.1, Biobase_2.8.0
| Sample_platform_id | GPL1261
| Sample_contact_name | Charles,Arthur,Whittaker
| Sample_contact_email | charliew@mit.edu
| Sample_contact_institute | Koch Institute
| Sample_contact_address | 77 Mass Ave 76-189
| Sample_contact_city | Cambridge
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02152
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM742nnn/GSM742808/suppl/GSM742808_CRE3.CEL.gz
| Sample_series_id | GSE30012
| Sample_data_row_count | 45037
| |
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